Mercurial > repos > recetox > matchms_split

comparison test-data/convert/msp_out.msp @ 23:6864944b00fd draft default tip

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planemo upload for repository https://github.com/RECETOX/galaxytools/tree/master/tools/matchms commit bd80a813fb2f01f22eed0c874f8911ce4d00762a
author recetox
date Mon, 30 Jun 2025 13:02:23 +0000
parents 9dfcee100f48
children
comparison
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22:ea6c5636c0cf 23:6864944b00fd
1 COMPOUND_NAME: Acephate
1 SCANNUMBER: 1161 2 SCANNUMBER: 1161
2 IONMODE: Positive 3 IONMODE: Positive
3 SPECTRUMTYPE: Centroid 4 SPECTRUMTYPE: Centroid
4 FORMULA: C4H10NO3PS 5 FORMULA: C4H10NO3PS
5 INCHIKEY: YASYVMFAVPKPKE-SECBINFHSA-N 6 INCHIKEY: YASYVMFAVPKPKE-SECBINFHSA-N
8 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 9 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
9 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 10 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
10 IONIZATION: ESI+ 11 IONIZATION: ESI+
11 LICENSE: CC BY-NC 12 LICENSE: CC BY-NC
12 COMMENT: 13 COMMENT:
13 COMPOUND_NAME: Acephate
14 RETENTION_TIME: 1.232997 14 RETENTION_TIME: 1.232997
15 PRECURSOR_MZ: 184.0194 15 PRECURSOR_MZ: 184.0194
16 ADDUCT: [M+H]+ 16 ADDUCT: [M+H]+
17 COLLISION_ENERGY: 17 COLLISION_ENERGY:
18 INSTRUMENT_TYPE: LC-ESI-Orbitrap 18 INSTRUMENT_TYPE: LC-ESI-Orbitrap
19 NUM PEAKS: 16 19 NUM PEAKS: 16
20 90.09368 1128.0 20 90.09368 1128.0
21 93.11512 1241.0 21 93.11512 1241.0
22 95.10279 1118.0 22 95.10279 1118.0
23 101.31465 1152.0 23 101.31465 1152.0
24 102.90688 1322.0 24 102.90688 1322.0
25 103.98039 1201.0 25 103.98039 1201.0
26 112.01607 12289.0 26 112.01607 12289.0
27 112.99994 38027.0 27 112.99994 38027.0
28 115.00399 1634.0 28 115.00399 1634.0
29 124.98121 922.0 29 124.98121 922.0
30 128.97701 9208.0 30 128.97701 9208.0
31 132.57193 1350.0 31 132.57193 1350.0
32 135.84808 1428.0 32 135.84808 1428.0
33 142.99275 16419.0 33 142.99275 16419.0
34 147.94205 1750.0 34 147.94205 1750.0
35 173.5094 2353.0 35 173.5094 2353.0
36 36
37 COMPOUND_NAME: Carbaryl
37 SCANNUMBER: 2257 38 SCANNUMBER: 2257
38 IONMODE: Positive 39 IONMODE: Positive
39 SPECTRUMTYPE: Centroid 40 SPECTRUMTYPE: Centroid
40 FORMULA: C12H11NO2 41 FORMULA: C12H11NO2
41 INCHIKEY: CVXBEEMKQHEXEN-UHFFFAOYSA-N 42 INCHIKEY: CVXBEEMKQHEXEN-UHFFFAOYSA-N
44 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 45 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
45 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 46 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
46 IONIZATION: ESI+ 47 IONIZATION: ESI+
47 LICENSE: CC BY-NC 48 LICENSE: CC BY-NC
48 COMMENT: 49 COMMENT:
49 COMPOUND_NAME: Carbaryl
50 RETENTION_TIME: 5.259445 50 RETENTION_TIME: 5.259445
51 PRECURSOR_MZ: 202.0863 51 PRECURSOR_MZ: 202.0863
52 ADDUCT: [M+H]+ 52 ADDUCT: [M+H]+
53 COLLISION_ENERGY: 53 COLLISION_ENERGY:
54 INSTRUMENT_TYPE: LC-ESI-Orbitrap 54 INSTRUMENT_TYPE: LC-ESI-Orbitrap
55 NUM PEAKS: 1 55 NUM PEAKS: 1
56 145.06491 1326147.0 56 145.06491 1326147.0
57 57
58 COMPOUND_NAME: Dicrotophos
58 SCANNUMBER: 1516 59 SCANNUMBER: 1516
59 IONMODE: Positive 60 IONMODE: Positive
60 SPECTRUMTYPE: Centroid 61 SPECTRUMTYPE: Centroid
61 FORMULA: C8H16NO5P 62 FORMULA: C8H16NO5P
62 INCHIKEY: VEENJGZXVHKXNB-UHFFFAOYSA-N 63 INCHIKEY: VEENJGZXVHKXNB-UHFFFAOYSA-N
65 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 66 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
66 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 67 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
67 IONIZATION: ESI+ 68 IONIZATION: ESI+
68 LICENSE: CC BY-NC 69 LICENSE: CC BY-NC
69 COMMENT: 70 COMMENT:
70 COMPOUND_NAME: Dicrotophos
71 RETENTION_TIME: 2.025499 71 RETENTION_TIME: 2.025499
72 PRECURSOR_MZ: 238.0844 72 PRECURSOR_MZ: 238.0844
73 ADDUCT: [M+H]+ 73 ADDUCT: [M+H]+
74 COLLISION_ENERGY: 74 COLLISION_ENERGY:
75 INSTRUMENT_TYPE: LC-ESI-Orbitrap 75 INSTRUMENT_TYPE: LC-ESI-Orbitrap
76 NUM PEAKS: 5 76 NUM PEAKS: 5
77 112.074 102027.0 77 112.074 102027.0
78 112.07591 9070987.0 78 112.07591 9070987.0
79 127.01563 3230337.0 79 127.01563 3230337.0
80 193.02605 7897744.0 80 193.02605 7897744.0
81 238.08437 2973124.0 81 238.08437 2973124.0
82 82
83 COMPOUND_NAME: Dimethoate
83 SCANNUMBER: 1865 84 SCANNUMBER: 1865
84 IONMODE: Positive 85 IONMODE: Positive
85 SPECTRUMTYPE: Centroid 86 SPECTRUMTYPE: Centroid
86 FORMULA: C5H12NO3PS2 87 FORMULA: C5H12NO3PS2
87 INCHIKEY: MCWXGJITAZMZEV-UHFFFAOYSA-N 88 INCHIKEY: MCWXGJITAZMZEV-UHFFFAOYSA-N
90 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 91 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
91 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 92 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
92 IONIZATION: ESI+ 93 IONIZATION: ESI+
93 LICENSE: CC BY-NC 94 LICENSE: CC BY-NC
94 COMMENT: 95 COMMENT:
95 COMPOUND_NAME: Dimethoate
96 RETENTION_TIME: 2.866696 96 RETENTION_TIME: 2.866696
97 PRECURSOR_MZ: 230.0072 97 PRECURSOR_MZ: 230.0072
98 ADDUCT: [M+H]+ 98 ADDUCT: [M+H]+
99 COLLISION_ENERGY: 99 COLLISION_ENERGY:
100 INSTRUMENT_TYPE: LC-ESI-Orbitrap 100 INSTRUMENT_TYPE: LC-ESI-Orbitrap
101 NUM PEAKS: 8 101 NUM PEAKS: 8
102 88.0219 548446.0 102 88.0219 548446.0
103 124.98233 183861.0 103 124.98233 183861.0
104 142.99275 722053.0 104 142.99275 722053.0
105 156.95422 80792.0 105 156.95422 80792.0
106 170.97 1426256.0 106 170.97 1426256.0
107 197.98123 240915.0 107 197.98123 240915.0
108 198.96501 5415933.0 108 198.96501 5415933.0
109 230.00722 497851.0 109 230.00722 497851.0
110 110
111 COMPOUND_NAME: Dimethomorph
111 SCANNUMBER: 3852 112 SCANNUMBER: 3852
112 IONMODE: Positive 113 IONMODE: Positive
113 SPECTRUMTYPE: Centroid 114 SPECTRUMTYPE: Centroid
114 FORMULA: C21H22NO4Cl 115 FORMULA: C21H22NO4Cl
115 INCHIKEY: QNBTYORWCCMPQP-UHFFFAOYSA-N 116 INCHIKEY: QNBTYORWCCMPQP-UHFFFAOYSA-N
118 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 119 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
119 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 120 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
120 IONIZATION: ESI+ 121 IONIZATION: ESI+
121 LICENSE: CC BY-NC 122 LICENSE: CC BY-NC
122 COMMENT: 123 COMMENT:
123 COMPOUND_NAME: Dimethomorph
124 RETENTION_TIME: 7.060486 124 RETENTION_TIME: 7.060486
125 PRECURSOR_MZ: 388.1316 125 PRECURSOR_MZ: 388.1316
126 ADDUCT: [M+H]+ 126 ADDUCT: [M+H]+
127 COLLISION_ENERGY: 127 COLLISION_ENERGY:
128 INSTRUMENT_TYPE: LC-ESI-Orbitrap 128 INSTRUMENT_TYPE: LC-ESI-Orbitrap
129 NUM PEAKS: 22 129 NUM PEAKS: 22
130 114.05532 468862.0 130 114.05532 468862.0
131 125.01571 886745.0 131 125.01571 886745.0
132 138.99484 4138370.0 132 138.99484 4138370.0
133 155.0705 425164.0 133 155.0705 425164.0
134 165.05519 15513399.0 134 165.05519 15513399.0
135 165.06543 350695.0 135 165.06543 350695.0
136 195.08057 386226.0 136 195.08057 386226.0
137 215.0262 490061.0 137 215.0262 490061.0
138 223.07544 702025.0 138 223.07544 702025.0
139 227.02576 230514.0 139 227.02576 230514.0
140 229.04225 216308.0 140 229.04225 216308.0
141 235.07555 241142.0 141 235.07555 241142.0
142 238.09914 1323577.0 142 238.09914 1323577.0
143 242.04929 2449236.0 143 242.04929 2449236.0
144 243.02142 891584.0 144 243.02142 891584.0
145 257.03726 578874.0 145 257.03726 578874.0
146 258.04443 3232295.0 146 258.04443 3232295.0
147 266.0943 358273.0 147 266.0943 358273.0
148 270.04492 608851.0 148 270.04492 608851.0
149 273.06772 3866006.0 149 273.06772 3866006.0
150 286.03912 483547.0 150 286.03912 483547.0
151 301.06311 4060551.0 151 301.06311 4060551.0
152 152
153 COMPOUND_NAME: Methamidophos
153 SCANNUMBER: 1009 154 SCANNUMBER: 1009
154 IONMODE: Positive 155 IONMODE: Positive
155 SPECTRUMTYPE: Centroid 156 SPECTRUMTYPE: Centroid
156 FORMULA: C2H8NO2PS 157 FORMULA: C2H8NO2PS
157 INCHIKEY: NNKVPIKMPCQWCG-ZCFIWIBFSA-N 158 INCHIKEY: NNKVPIKMPCQWCG-ZCFIWIBFSA-N
160 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 161 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
161 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 162 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
162 IONIZATION: ESI+ 163 IONIZATION: ESI+
163 LICENSE: CC BY-NC 164 LICENSE: CC BY-NC
164 COMMENT: 165 COMMENT:
165 COMPOUND_NAME: Methamidophos
166 RETENTION_TIME: 1.153307 166 RETENTION_TIME: 1.153307
167 PRECURSOR_MZ: 142.0089 167 PRECURSOR_MZ: 142.0089
168 ADDUCT: [M+H]+ 168 ADDUCT: [M+H]+
169 COLLISION_ENERGY: 169 COLLISION_ENERGY:
170 INSTRUMENT_TYPE: LC-ESI-Orbitrap 170 INSTRUMENT_TYPE: LC-ESI-Orbitrap
171 NUM PEAKS: 4 171 NUM PEAKS: 4
172 98.00042 37721.0 172 98.00042 37721.0
173 109.98272 71172.0 173 109.98272 71172.0
174 112.01607 2867923.0 174 112.01607 2867923.0
175 127.99321 75837.0 175 127.99321 75837.0
176 176
177 COMPOUND_NAME: Mevinphos
177 SCANNUMBER: 1924 178 SCANNUMBER: 1924
178 IONMODE: Positive 179 IONMODE: Positive
179 SPECTRUMTYPE: Centroid 180 SPECTRUMTYPE: Centroid
180 FORMULA: C7H13O6P 181 FORMULA: C7H13O6P
181 INCHIKEY: GEPDYQSQVLXLEU-UHFFFAOYSA-N 182 INCHIKEY: GEPDYQSQVLXLEU-UHFFFAOYSA-N
184 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 185 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
185 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 186 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
186 IONIZATION: ESI+ 187 IONIZATION: ESI+
187 LICENSE: CC BY-NC 188 LICENSE: CC BY-NC
188 COMMENT: 189 COMMENT:
189 COMPOUND_NAME: Mevinphos
190 RETENTION_TIME: 2.876307 190 RETENTION_TIME: 2.876307
191 PRECURSOR_MZ: 225.0525 191 PRECURSOR_MZ: 225.0525
192 ADDUCT: [M+H]+ 192 ADDUCT: [M+H]+
193 COLLISION_ENERGY: 193 COLLISION_ENERGY:
194 INSTRUMENT_TYPE: LC-ESI-Orbitrap 194 INSTRUMENT_TYPE: LC-ESI-Orbitrap
195 NUM PEAKS: 4 195 NUM PEAKS: 4
196 99.04416 295529.0 196 99.04416 295529.0
197 127.01563 1960973.0 197 127.01563 1960973.0
198 193.02605 1150190.0 198 193.02605 1150190.0
199 225.05209 101872.0 199 225.05209 101872.0
200 200
201 COMPOUND_NAME: Omethoate
201 SCANNUMBER: 1246 202 SCANNUMBER: 1246
202 IONMODE: Positive 203 IONMODE: Positive
203 SPECTRUMTYPE: Centroid 204 SPECTRUMTYPE: Centroid
204 FORMULA: C5H12NO4PS 205 FORMULA: C5H12NO4PS
205 INCHIKEY: PZXOQEXFMJCDPG-UHFFFAOYSA-N 206 INCHIKEY: PZXOQEXFMJCDPG-UHFFFAOYSA-N
208 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 209 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
209 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 210 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
210 IONIZATION: ESI+ 211 IONIZATION: ESI+
211 LICENSE: CC BY-NC 212 LICENSE: CC BY-NC
212 COMMENT: 213 COMMENT:
213 COMPOUND_NAME: Omethoate
214 RETENTION_TIME: 1.33423 214 RETENTION_TIME: 1.33423
215 PRECURSOR_MZ: 214.0303 215 PRECURSOR_MZ: 214.0303
216 ADDUCT: [M+H]+ 216 ADDUCT: [M+H]+
217 COLLISION_ENERGY: 217 COLLISION_ENERGY:
218 INSTRUMENT_TYPE: LC-ESI-Orbitrap 218 INSTRUMENT_TYPE: LC-ESI-Orbitrap
219 NUM PEAKS: 5 219 NUM PEAKS: 5
220 104.01654 86844.0 220 104.01654 86844.0
221 124.98233 194375.0 221 124.98233 194375.0
222 127.01563 4696021.0 222 127.01563 4696021.0
223 128.97701 47970.0 223 128.97701 47970.0
224 142.99275 4310988.0 224 142.99275 4310988.0
225 225
226 COMPOUND_NAME: Temephos
226 SCANNUMBER: 5447 227 SCANNUMBER: 5447
227 IONMODE: Positive 228 IONMODE: Positive
228 SPECTRUMTYPE: Centroid 229 SPECTRUMTYPE: Centroid
229 FORMULA: C16H20O6P2S3 230 FORMULA: C16H20O6P2S3
230 INCHIKEY: WWJZWCUNLNYYAU-UHFFFAOYSA-N 231 INCHIKEY: WWJZWCUNLNYYAU-UHFFFAOYSA-N
233 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 234 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
234 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 235 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
235 IONIZATION: ESI+ 236 IONIZATION: ESI+
236 LICENSE: CC BY-NC 237 LICENSE: CC BY-NC
237 COMMENT: 238 COMMENT:
238 COMPOUND_NAME: Temephos
239 RETENTION_TIME: 7.736881 239 RETENTION_TIME: 7.736881
240 PRECURSOR_MZ: 466.9978 240 PRECURSOR_MZ: 466.9978
241 ADDUCT: [M+H]+ 241 ADDUCT: [M+H]+
242 COLLISION_ENERGY: 242 COLLISION_ENERGY:
243 INSTRUMENT_TYPE: LC-ESI-Orbitrap 243 INSTRUMENT_TYPE: LC-ESI-Orbitrap
244 NUM PEAKS: 44 244 NUM PEAKS: 44
245 124.98233 218400.0 245 124.98233 218400.0
246 125.00596 124192.0 246 125.00596 124192.0
247 127.01563 590561.0 247 127.01563 590561.0
248 139.02167 79978.0 248 139.02167 79978.0
249 139.05467 105470.0 249 139.05467 105470.0
250 140.95975 428071.0 250 140.95975 428071.0
251 142.99275 7482486.0 251 142.99275 7482486.0
252 154.99849 619650.0 252 154.99849 619650.0
253 157.00861 365474.0 253 157.00861 365474.0
254 171.02641 502869.0 254 171.02641 502869.0
255 172.03448 151150.0 255 172.03448 151150.0
256 183.02695 176056.0 256 183.02695 176056.0
257 184.03453 206568.0 257 184.03453 206568.0
258 187.02121 240339.0 258 187.02121 240339.0
259 199.02151 245544.0 259 199.02151 245544.0
260 200.02902 385101.0 260 200.02902 385101.0
261 201.03729 198527.0 261 201.03729 198527.0
262 211.03268 88063.0 262 211.03268 88063.0
263 215.01689 538632.0 263 215.01689 538632.0
264 217.03214 259530.0 264 217.03214 259530.0
265 218.98798 87371.0 265 218.98798 87371.0
266 219.02972 94609.0 266 219.02972 94609.0
267 230.99336 108101.0 267 230.99336 108101.0
268 232.03233 244260.0 268 232.03233 244260.0
269 233.00958 88058.0 269 233.00958 88058.0
270 247.02538 224924.0 270 247.02538 224924.0
271 248.03291 127038.0 271 248.03291 127038.0
272 261.98486 132283.0 272 261.98486 132283.0
273 262.99268 185876.0 273 262.99268 185876.0
274 264.00052 186556.0 274 264.00052 186556.0
275 278.98856 208891.0 275 278.98856 208891.0
276 293.00336 81563.0 276 293.00336 81563.0
277 293.99384 84250.0 277 293.99384 84250.0
278 294.96494 87413.0 278 294.96494 87413.0
279 296.99844 481380.0 279 296.99844 481380.0
280 298.0065 151600.0 280 298.0065 151600.0
281 311.01453 119733.0 281 311.01453 119733.0
282 313.01282 181581.0 282 313.01282 181581.0
283 327.99893 299098.0 283 327.99893 299098.0
284 341.00787 2218540.0 284 341.00787 2218540.0
285 342.01566 293721.0 285 342.01566 293721.0
286 356.03104 227870.0 286 356.03104 227870.0
287 357.03922 75786.0 287 357.03922 75786.0
288 387.9765 125383.0 288 387.9765 125383.0
289 289
290 COMPOUND_NAME: Trichlorfon
290 SCANNUMBER: 1625 291 SCANNUMBER: 1625
291 IONMODE: Positive 292 IONMODE: Positive
292 SPECTRUMTYPE: Centroid 293 SPECTRUMTYPE: Centroid
293 FORMULA: C4H8O4Cl3P 294 FORMULA: C4H8O4Cl3P
294 INCHIKEY: NFACJZMKEDPNKN-VKHMYHEASA-N 295 INCHIKEY: NFACJZMKEDPNKN-VKHMYHEASA-N
297 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 298 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
298 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 299 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
299 IONIZATION: ESI+ 300 IONIZATION: ESI+
300 LICENSE: CC BY-NC 301 LICENSE: CC BY-NC
301 COMMENT: 302 COMMENT:
302 COMPOUND_NAME: Trichlorfon
303 RETENTION_TIME: 2.242985 303 RETENTION_TIME: 2.242985
304 PRECURSOR_MZ: 256.9308 304 PRECURSOR_MZ: 256.9308
305 ADDUCT: [M+H]+ 305 ADDUCT: [M+H]+
306 COLLISION_ENERGY: 306 COLLISION_ENERGY:
307 INSTRUMENT_TYPE: LC-ESI-Orbitrap 307 INSTRUMENT_TYPE: LC-ESI-Orbitrap
308 NUM PEAKS: 4 308 NUM PEAKS: 4
309 93.01007 104589.0 309 93.01007 104589.0
310 97.00512 72293.0 310 97.00512 72293.0
311 112.99994 32292.0 311 112.99994 32292.0
312 127.01563 3150219.0 312 127.01563 3150219.0
313 313
314 COMPOUND_NAME: Vamidothion
314 SCANNUMBER: 2002 315 SCANNUMBER: 2002
315 IONMODE: Positive 316 IONMODE: Positive
316 SPECTRUMTYPE: Centroid 317 SPECTRUMTYPE: Centroid
317 FORMULA: C8H18NO4PS2 318 FORMULA: C8H18NO4PS2
318 INCHIKEY: LESVOLZBIFDZGS-ZETCQYMHSA-N 319 INCHIKEY: LESVOLZBIFDZGS-ZETCQYMHSA-N
321 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 322 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
322 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 323 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
323 IONIZATION: ESI+ 324 IONIZATION: ESI+
324 LICENSE: CC BY-NC 325 LICENSE: CC BY-NC
325 COMMENT: 326 COMMENT:
326 COMPOUND_NAME: Vamidothion
327 RETENTION_TIME: 2.914602 327 RETENTION_TIME: 2.914602
328 PRECURSOR_MZ: 288.0491 328 PRECURSOR_MZ: 288.0491
329 ADDUCT: [M+H]+ 329 ADDUCT: [M+H]+
330 COLLISION_ENERGY: 330 COLLISION_ENERGY:
331 INSTRUMENT_TYPE: LC-ESI-Orbitrap 331 INSTRUMENT_TYPE: LC-ESI-Orbitrap
332 NUM PEAKS: 3 332 NUM PEAKS: 3
333 118.03215 464396.0 333 118.03215 464396.0
334 146.06366 10321336.0 334 146.06366 10321336.0
335 288.04907 1456244.0 335 288.04907 1456244.0
336 336
337 COMPOUND_NAME: Aldicarb sulfone
337 SCANNUMBER: 1209 338 SCANNUMBER: 1209
338 IONMODE: Positive 339 IONMODE: Positive
339 SPECTRUMTYPE: Centroid 340 SPECTRUMTYPE: Centroid
340 FORMULA: C7H14N2O4S 341 FORMULA: C7H14N2O4S
341 INCHIKEY: YRRKLBAKDXSTNC-UHFFFAOYSA-N 342 INCHIKEY: YRRKLBAKDXSTNC-UHFFFAOYSA-N
344 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 345 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
345 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 346 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
346 IONIZATION: ESI+ 347 IONIZATION: ESI+
347 LICENSE: CC BY-NC 348 LICENSE: CC BY-NC
348 COMMENT: 349 COMMENT:
349 COMPOUND_NAME: Aldicarb sulfone
350 RETENTION_TIME: 1.483623 350 RETENTION_TIME: 1.483623
351 PRECURSOR_MZ: 223.075 351 PRECURSOR_MZ: 223.075
352 ADDUCT: [M+H]+ 352 ADDUCT: [M+H]+
353 COLLISION_ENERGY: 353 COLLISION_ENERGY:
354 INSTRUMENT_TYPE: LC-ESI-Orbitrap 354 INSTRUMENT_TYPE: LC-ESI-Orbitrap
355 NUM PEAKS: 9 355 NUM PEAKS: 9
356 86.06018 763151.0 356 86.06018 763151.0
357 106.03234 330646.0 357 106.03234 330646.0
358 120.04782 16624.0 358 120.04782 16624.0
359 148.03964 11931.0 359 148.03964 11931.0
360 148.04301 1170924.0 360 148.04301 1170924.0
361 166.05334 738329.0 361 166.05334 738329.0
362 208.9567 12192.0 362 208.9567 12192.0
363 223.06381 99297.0 363 223.06381 99297.0
364 223.07454 90546.0 364 223.07454 90546.0
365 365
366 COMPOUND_NAME: Benfuracarb
366 SCANNUMBER: 4766 367 SCANNUMBER: 4766
367 IONMODE: Positive 368 IONMODE: Positive
368 SPECTRUMTYPE: Centroid 369 SPECTRUMTYPE: Centroid
369 FORMULA: C20H30N2O5S 370 FORMULA: C20H30N2O5S
370 INCHIKEY: FYZBOYWSHKHDMT-UHFFFAOYSA-N 371 INCHIKEY: FYZBOYWSHKHDMT-UHFFFAOYSA-N
373 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 374 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
374 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 375 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
375 IONIZATION: ESI+ 376 IONIZATION: ESI+
376 LICENSE: CC BY-NC 377 LICENSE: CC BY-NC
377 COMMENT: 378 COMMENT:
378 COMPOUND_NAME: Benfuracarb
379 RETENTION_TIME: 7.163228 379 RETENTION_TIME: 7.163228
380 PRECURSOR_MZ: 411.1956 380 PRECURSOR_MZ: 411.1956
381 ADDUCT: [M+H]+ 381 ADDUCT: [M+H]+
382 COLLISION_ENERGY: 382 COLLISION_ENERGY:
383 INSTRUMENT_TYPE: LC-ESI-Orbitrap 383 INSTRUMENT_TYPE: LC-ESI-Orbitrap
384 NUM PEAKS: 22 384 NUM PEAKS: 22
385 90.03748 30498.0 385 90.03748 30498.0
386 102.00096 69259.0 386 102.00096 69259.0
387 109.02874 31641.0 387 109.02874 31641.0
388 111.08049 29319.0 388 111.08049 29319.0
389 112.07591 44046.0 389 112.07591 44046.0
390 115.05431 43630.0 390 115.05431 43630.0
391 116.07085 30236.0 391 116.07085 30236.0
392 125.00558 53990.0 392 125.00558 53990.0
393 133.0649 58728.0 393 133.0649 58728.0
394 137.05998 23811.0 394 137.05998 23811.0
395 143.04921 51685.0 395 143.04921 51685.0
396 144.05734 107852.0 396 144.05734 107852.0
397 149.04198 61180.0 397 149.04198 61180.0
398 153.0369 175741.0 398 153.0369 175741.0
399 158.11797 70456.0 399 158.11797 70456.0
400 161.06012 99721.0 400 161.06012 99721.0
401 162.0676 971826.0 401 162.0676 971826.0
402 167.01654 45521.0 402 167.01654 45521.0
403 167.05246 131346.0 403 167.05246 131346.0
404 171.0114 23364.0 404 171.0114 23364.0
405 177.03709 172641.0 405 177.03709 172641.0
406 195.04765 2265269.0 406 195.04765 2265269.0
407 407
408 COMPOUND_NAME: Butoxycarboxim
408 SCANNUMBER: 1209 409 SCANNUMBER: 1209
409 IONMODE: Positive 410 IONMODE: Positive
410 SPECTRUMTYPE: Centroid 411 SPECTRUMTYPE: Centroid
411 FORMULA: C7H14N2O4S 412 FORMULA: C7H14N2O4S
412 INCHIKEY: CTJBHIROCMPUKL-HOITVRGQSA-N 413 INCHIKEY: CTJBHIROCMPUKL-HOITVRGQSA-N
415 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 416 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
416 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 417 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
417 IONIZATION: ESI+ 418 IONIZATION: ESI+
418 LICENSE: CC BY-NC 419 LICENSE: CC BY-NC
419 COMMENT: 420 COMMENT:
420 COMPOUND_NAME: Butoxycarboxim
421 RETENTION_TIME: 1.483623 421 RETENTION_TIME: 1.483623
422 PRECURSOR_MZ: 223.075 422 PRECURSOR_MZ: 223.075
423 ADDUCT: [M+H]+ 423 ADDUCT: [M+H]+
424 COLLISION_ENERGY: 424 COLLISION_ENERGY:
425 INSTRUMENT_TYPE: LC-ESI-Orbitrap 425 INSTRUMENT_TYPE: LC-ESI-Orbitrap
426 NUM PEAKS: 9 426 NUM PEAKS: 9
427 86.06018 763151.0 427 86.06018 763151.0
428 106.03234 330646.0 428 106.03234 330646.0
429 120.04782 16624.0 429 120.04782 16624.0
430 148.03964 11931.0 430 148.03964 11931.0
431 148.04301 1170924.0 431 148.04301 1170924.0
432 166.05334 738329.0 432 166.05334 738329.0
433 208.9567 12192.0 433 208.9567 12192.0
434 223.06381 99297.0 434 223.06381 99297.0
435 223.07454 90546.0 435 223.07454 90546.0
436 436
437 COMPOUND_NAME: Furathiocarb
437 SCANNUMBER: 4928 438 SCANNUMBER: 4928
438 IONMODE: Positive 439 IONMODE: Positive
439 SPECTRUMTYPE: Centroid 440 SPECTRUMTYPE: Centroid
440 FORMULA: C18H26N2O5S 441 FORMULA: C18H26N2O5S
441 INCHIKEY: HAWJXYBZNNRMNO-UHFFFAOYSA-N 442 INCHIKEY: HAWJXYBZNNRMNO-UHFFFAOYSA-N
444 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 445 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
445 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 446 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
446 IONIZATION: ESI+ 447 IONIZATION: ESI+
447 LICENSE: CC BY-NC 448 LICENSE: CC BY-NC
448 COMMENT: 449 COMMENT:
449 COMPOUND_NAME: Furathiocarb
450 RETENTION_TIME: 7.19165 450 RETENTION_TIME: 7.19165
451 PRECURSOR_MZ: 383.1642 451 PRECURSOR_MZ: 383.1642
452 ADDUCT: [M+H]+ 452 ADDUCT: [M+H]+
453 COLLISION_ENERGY: 453 COLLISION_ENERGY:
454 INSTRUMENT_TYPE: LC-ESI-Orbitrap 454 INSTRUMENT_TYPE: LC-ESI-Orbitrap
455 NUM PEAKS: 49 455 NUM PEAKS: 49
456 87.02665 170322.0 456 87.02665 170322.0
457 90.03748 426298.0 457 90.03748 426298.0
458 91.05442 232061.0 458 91.05442 232061.0
459 95.04954 175219.0 459 95.04954 175219.0
460 97.01102 504855.0 460 97.01102 504855.0
461 105.0702 848188.0 461 105.0702 848188.0
462 107.04936 404555.0 462 107.04936 404555.0
463 107.08593 329012.0 463 107.08593 329012.0
464 109.02874 370826.0 464 109.02874 370826.0
465 109.0651 289619.0 465 109.0651 289619.0
466 111.0808 200502.0 466 111.0808 200502.0
467 115.05464 651489.0 467 115.05464 651489.0
468 116.06246 367386.0 468 116.06246 367386.0
469 117.07032 300497.0 469 117.07032 300497.0
470 118.07793 135317.0 470 118.07793 135317.0
471 121.06524 216247.0 471 121.06524 216247.0
472 122.03665 593314.0 472 122.03665 593314.0
473 123.04434 862460.0 473 123.04434 862460.0
474 125.00596 4842440.0 474 125.00596 4842440.0
475 131.04935 572523.0 475 131.04935 572523.0
476 133.0649 1461373.0 476 133.0649 1461373.0
477 134.01871 277355.0 477 134.01871 277355.0
478 134.07285 254631.0 478 134.07285 254631.0
479 135.08093 991426.0 479 135.08093 991426.0
480 137.05998 186090.0 480 137.05998 186090.0
481 139.02167 356706.0 481 139.02167 356706.0
482 139.05775 475631.0 482 139.05775 475631.0
483 143.04967 427124.0 483 143.04967 427124.0
484 144.05734 1163702.0 484 144.05734 1163702.0
485 145.0649 273080.0 485 145.0649 273080.0
486 146.07314 822073.0 486 146.07314 822073.0
487 147.04451 460929.0 487 147.04451 460929.0
488 147.08089 234097.0 488 147.08089 234097.0
489 149.00584 154496.0 489 149.00584 154496.0
490 149.04247 1446405.0 490 149.04247 1446405.0
491 149.06004 3536863.0 491 149.06004 3536863.0
492 153.00082 192002.0 492 153.00082 192002.0
493 153.0374 1282857.0 493 153.0374 1282857.0
494 161.06012 1492726.0 494 161.06012 1492726.0
495 162.0676 9461931.0 495 162.0676 9461931.0
496 163.07562 216378.0 496 163.07562 216378.0
497 164.08348 6924294.0 497 164.08348 6924294.0
498 165.09103 228313.0 498 165.09103 228313.0
499 167.01654 354658.0 499 167.01654 354658.0
500 167.05304 10929155.0 500 167.05304 10929155.0
501 171.0114 128914.0 501 171.0114 128914.0
502 177.03709 3978125.0 502 177.03709 3978125.0
503 180.02414 213051.0 503 180.02414 213051.0
504 195.04765 11849349.0 504 195.04765 11849349.0
505 505
506 COMPOUND_NAME: Methabenzthiazuron
506 SCANNUMBER: 3333 507 SCANNUMBER: 3333
507 IONMODE: Positive 508 IONMODE: Positive
508 SPECTRUMTYPE: Centroid 509 SPECTRUMTYPE: Centroid
509 FORMULA: C10H11N3OS 510 FORMULA: C10H11N3OS
510 INCHIKEY: RRVIAQKBTUQODI-UHFFFAOYSA-N 511 INCHIKEY: RRVIAQKBTUQODI-UHFFFAOYSA-N
513 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 514 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
514 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 515 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
515 IONIZATION: ESI+ 516 IONIZATION: ESI+
516 LICENSE: CC BY-NC 517 LICENSE: CC BY-NC
517 COMMENT: 518 COMMENT:
518 COMPOUND_NAME: Methabenzthiazuron
519 RETENTION_TIME: 6.711947 519 RETENTION_TIME: 6.711947
520 PRECURSOR_MZ: 222.0702 520 PRECURSOR_MZ: 222.0702
521 ADDUCT: [M+H]+ 521 ADDUCT: [M+H]+
522 COLLISION_ENERGY: 522 COLLISION_ENERGY:
523 INSTRUMENT_TYPE: LC-ESI-Orbitrap 523 INSTRUMENT_TYPE: LC-ESI-Orbitrap
524 NUM PEAKS: 8 524 NUM PEAKS: 8
525 92.0498 456372.0 525 92.0498 456372.0
526 109.01102 367319.0 526 109.01102 367319.0
527 123.01394 375280.0 527 123.01394 375280.0
528 124.02193 2568680.0 528 124.02193 2568680.0
529 132.06825 123566.0 529 132.06825 123566.0
530 150.02492 9399192.0 530 150.02492 9399192.0
531 163.03316 152108.0 531 163.03316 152108.0
532 165.04836 9598566.0 532 165.04836 9598566.0
533 533
534 COMPOUND_NAME: Tebuthiuron
534 SCANNUMBER: 1984 535 SCANNUMBER: 1984
535 IONMODE: Positive 536 IONMODE: Positive
536 SPECTRUMTYPE: Centroid 537 SPECTRUMTYPE: Centroid
537 FORMULA: C9H16N4OS 538 FORMULA: C9H16N4OS
538 INCHIKEY: HBPDKDSFLXWOAE-UHFFFAOYSA-N 539 INCHIKEY: HBPDKDSFLXWOAE-UHFFFAOYSA-N
541 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 542 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
542 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 543 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
543 IONIZATION: ESI+ 544 IONIZATION: ESI+
544 LICENSE: CC BY-NC 545 LICENSE: CC BY-NC
545 COMMENT: 546 COMMENT:
546 COMPOUND_NAME: Tebuthiuron
547 RETENTION_TIME: 4.241355 547 RETENTION_TIME: 4.241355
548 PRECURSOR_MZ: 229.1121 548 PRECURSOR_MZ: 229.1121
549 ADDUCT: [M+H]+ 549 ADDUCT: [M+H]+
550 COLLISION_ENERGY: 550 COLLISION_ENERGY:
551 INSTRUMENT_TYPE: LC-ESI-Orbitrap 551 INSTRUMENT_TYPE: LC-ESI-Orbitrap
552 NUM PEAKS: 9 552 NUM PEAKS: 9
553 88.0219 230604.0 553 88.0219 230604.0
554 89.01719 2030070.0 554 89.01719 2030070.0
555 101.04233 435137.0 555 101.04233 435137.0
556 116.0279 20609154.0 556 116.0279 20609154.0
557 141.04826 319289.0 557 141.04826 319289.0
558 142.04346 1851694.0 558 142.04346 1851694.0
559 156.05936 1133851.0 559 156.05936 1133851.0
560 157.06721 6762498.0 560 157.06721 6762498.0
561 172.09081 12592908.0 561 172.09081 12592908.0
562 562
563 COMPOUND_NAME: Thidiazuron
563 SCANNUMBER: 2185 564 SCANNUMBER: 2185
564 IONMODE: Positive 565 IONMODE: Positive
565 SPECTRUMTYPE: Centroid 566 SPECTRUMTYPE: Centroid
566 FORMULA: C9H8N4OS 567 FORMULA: C9H8N4OS
567 INCHIKEY: HFCYZXMHUIHAQI-UHFFFAOYSA-N 568 INCHIKEY: HFCYZXMHUIHAQI-UHFFFAOYSA-N
570 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 571 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
571 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 572 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
572 IONIZATION: ESI+ 573 IONIZATION: ESI+
573 LICENSE: CC BY-NC 574 LICENSE: CC BY-NC
574 COMMENT: 575 COMMENT:
575 COMPOUND_NAME: Thidiazuron
576 RETENTION_TIME: 4.909884 576 RETENTION_TIME: 4.909884
577 PRECURSOR_MZ: 221.0497 577 PRECURSOR_MZ: 221.0497
578 ADDUCT: [M+H]+ 578 ADDUCT: [M+H]+
579 COLLISION_ENERGY: 579 COLLISION_ENERGY:
580 INSTRUMENT_TYPE: LC-ESI-Orbitrap 580 INSTRUMENT_TYPE: LC-ESI-Orbitrap
581 NUM PEAKS: 7 581 NUM PEAKS: 7
582 92.04957 154355.0 582 92.04957 154355.0
583 94.0652 188105.0 583 94.0652 188105.0
584 95.04929 172328.0 584 95.04929 172328.0
585 102.0123 2547264.0 585 102.0123 2547264.0
586 105.04477 127605.0 586 105.04477 127605.0
587 120.04464 76344.0 587 120.04464 76344.0
588 127.99126 615346.0 588 127.99126 615346.0
589 589
590 COMPOUND_NAME: Ethiofencarb
590 SCANNUMBER: 2307 591 SCANNUMBER: 2307
591 IONMODE: Positive 592 IONMODE: Positive
592 SPECTRUMTYPE: Centroid 593 SPECTRUMTYPE: Centroid
593 FORMULA: C11H15NO2S 594 FORMULA: C11H15NO2S
594 INCHIKEY: HEZNVIYQEUHLNI-UHFFFAOYSA-N 595 INCHIKEY: HEZNVIYQEUHLNI-UHFFFAOYSA-N
597 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 598 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
598 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 599 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
599 IONIZATION: ESI+ 600 IONIZATION: ESI+
600 LICENSE: CC BY-NC 601 LICENSE: CC BY-NC
601 COMMENT: 602 COMMENT:
602 COMPOUND_NAME: Ethiofencarb
603 RETENTION_TIME: 5.074083 603 RETENTION_TIME: 5.074083
604 PRECURSOR_MZ: 226.09 604 PRECURSOR_MZ: 226.09
605 ADDUCT: [M+H]+ 605 ADDUCT: [M+H]+
606 COLLISION_ENERGY: 606 COLLISION_ENERGY:
607 INSTRUMENT_TYPE: LC-ESI-Orbitrap 607 INSTRUMENT_TYPE: LC-ESI-Orbitrap
608 NUM PEAKS: 6 608 NUM PEAKS: 6
609 95.04929 42106.0 609 95.04929 42106.0
610 105.04477 32913.0 610 105.04477 32913.0
611 107.04936 243964.0 611 107.04936 243964.0
612 120.08101 4266.0 612 120.08101 4266.0
613 134.0966 5759.0 613 134.0966 5759.0
614 147.93529 2678.0 614 147.93529 2678.0
615 615
616 COMPOUND_NAME: Methiocarb
616 SCANNUMBER: 2724 617 SCANNUMBER: 2724
617 IONMODE: Positive 618 IONMODE: Positive
618 SPECTRUMTYPE: Centroid 619 SPECTRUMTYPE: Centroid
619 FORMULA: C11H15NO2S 620 FORMULA: C11H15NO2S
620 INCHIKEY: YFBPRJGDJKVWAH-UHFFFAOYSA-N 621 INCHIKEY: YFBPRJGDJKVWAH-UHFFFAOYSA-N
623 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 624 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
624 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 625 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
625 IONIZATION: ESI+ 626 IONIZATION: ESI+
626 LICENSE: CC BY-NC 627 LICENSE: CC BY-NC
627 COMMENT: 628 COMMENT:
628 COMPOUND_NAME: Methiocarb
629 RETENTION_TIME: 6.352629 629 RETENTION_TIME: 6.352629
630 PRECURSOR_MZ: 226.0899 630 PRECURSOR_MZ: 226.0899
631 ADDUCT: [M+H]+ 631 ADDUCT: [M+H]+
632 COLLISION_ENERGY: 632 COLLISION_ENERGY:
633 INSTRUMENT_TYPE: LC-ESI-Orbitrap 633 INSTRUMENT_TYPE: LC-ESI-Orbitrap
634 NUM PEAKS: 4 634 NUM PEAKS: 4
635 121.06488 799606.0 635 121.06488 799606.0
636 122.07284 96691.0 636 122.07284 96691.0
637 169.06853 4882474.0 637 169.06853 4882474.0
638 226.08951 145633.0 638 226.08951 145633.0
639 639
640 COMPOUND_NAME: Carbofuran
640 SCANNUMBER: 1753 641 SCANNUMBER: 1753
641 IONMODE: Positive 642 IONMODE: Positive
642 SPECTRUMTYPE: Centroid 643 SPECTRUMTYPE: Centroid
643 FORMULA: C12H15NO3 644 FORMULA: C12H15NO3
644 INCHIKEY: DUEPRVBVGDRKAG-UHFFFAOYSA-N 645 INCHIKEY: DUEPRVBVGDRKAG-UHFFFAOYSA-N
647 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 648 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
648 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 649 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
649 IONIZATION: ESI+ 650 IONIZATION: ESI+
650 LICENSE: CC BY-NC 651 LICENSE: CC BY-NC
651 COMMENT: 652 COMMENT:
652 COMPOUND_NAME: Carbofuran
653 RETENTION_TIME: 4.14677 653 RETENTION_TIME: 4.14677
654 PRECURSOR_MZ: 222.1128 654 PRECURSOR_MZ: 222.1128
655 ADDUCT: [M+H]+ 655 ADDUCT: [M+H]+
656 COLLISION_ENERGY: 656 COLLISION_ENERGY:
657 INSTRUMENT_TYPE: LC-ESI-Orbitrap 657 INSTRUMENT_TYPE: LC-ESI-Orbitrap
658 NUM PEAKS: 10 658 NUM PEAKS: 10
659 91.05442 804154.0 659 91.05442 804154.0
660 95.04929 737907.0 660 95.04929 737907.0
661 105.03379 225770.0 661 105.03379 225770.0
662 105.04506 153330.0 662 105.04506 153330.0
663 111.04436 105844.0 663 111.04436 105844.0
664 119.04944 164758.0 664 119.04944 164758.0
665 119.0857 227890.0 665 119.0857 227890.0
666 123.04434 10121862.0 666 123.04434 10121862.0
667 137.05997 448261.0 667 137.05997 448261.0
668 147.08089 104307.0 668 147.08089 104307.0
669 669
670 COMPOUND_NAME: Chloroxuron
670 SCANNUMBER: 4866 671 SCANNUMBER: 4866
671 IONMODE: Positive 672 IONMODE: Positive
672 SPECTRUMTYPE: Centroid 673 SPECTRUMTYPE: Centroid
673 FORMULA: C15H15N2O2Cl 674 FORMULA: C15H15N2O2Cl
674 INCHIKEY: IVUXTESCPZUGJC-UHFFFAOYSA-N 675 INCHIKEY: IVUXTESCPZUGJC-UHFFFAOYSA-N
677 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 678 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
678 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 679 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
679 IONIZATION: ESI+ 680 IONIZATION: ESI+
680 LICENSE: CC BY-NC 681 LICENSE: CC BY-NC
681 COMMENT: 682 COMMENT:
682 COMPOUND_NAME: Chloroxuron
683 RETENTION_TIME: 6.824893 683 RETENTION_TIME: 6.824893
684 PRECURSOR_MZ: 291.09 684 PRECURSOR_MZ: 291.09
685 ADDUCT: [M+H]+ 685 ADDUCT: [M+H]+
686 COLLISION_ENERGY: 686 COLLISION_ENERGY:
687 INSTRUMENT_TYPE: LC-ESI-Orbitrap 687 INSTRUMENT_TYPE: LC-ESI-Orbitrap
688 NUM PEAKS: 34 688 NUM PEAKS: 34
689 94.04169 27706.0 689 94.04169 27706.0
690 98.99973 58512.0 690 98.99973 58512.0
691 106.06546 243512.0 691 106.06546 243512.0
692 118.06519 562204.0 692 118.06519 562204.0
693 119.07315 45536.0 693 119.07315 45536.0
694 120.081 78773.0 694 120.081 78773.0
695 126.99488 83528.0 695 126.99488 83528.0
696 128.06239 310868.0 696 128.06239 310868.0
697 129.01042 87060.0 697 129.01042 87060.0
698 139.00583 288886.0 698 139.00583 288886.0
699 145.0649 99810.0 699 145.0649 99810.0
700 146.06033 24021.0 700 146.06033 24021.0
701 147.06796 35662.0 701 147.06796 35662.0
702 149.01559 36207.0 702 149.01559 36207.0
703 152.00261 21619.0 703 152.00261 21619.0
704 154.06534 101982.0 704 154.06534 101982.0
705 155.06065 198243.0 705 155.06065 198243.0
706 155.07309 108829.0 706 155.07309 108829.0
707 163.03091 1196885.0 707 163.03091 1196885.0
708 163.08679 138657.0 708 163.08679 138657.0
709 164.09476 19883.0 709 164.09476 19883.0
710 168.05711 61850.0 710 168.05711 61850.0
711 173.50755 33783.0 711 173.50755 33783.0
712 175.03131 42262.0 712 175.03131 42262.0
713 182.05989 34322.0 713 182.05989 34322.0
714 183.06813 160230.0 714 183.06813 160230.0
715 190.04181 279261.0 715 190.04181 279261.0
716 191.02574 49125.0 716 191.02574 49125.0
717 211.06313 28451.0 717 211.06313 28451.0
718 218.03699 1977628.0 718 218.03699 1977628.0
719 219.04449 20961.0 719 219.04449 20961.0
720 233.15379 75598.0 720 233.15379 75598.0
721 246.03224 40845.0 721 246.03224 40845.0
722 249.18484 96150.0 722 249.18484 96150.0
723 723
724 COMPOUND_NAME: Chlortoluron
724 SCANNUMBER: 2586 725 SCANNUMBER: 2586
725 IONMODE: Positive 726 IONMODE: Positive
726 SPECTRUMTYPE: Centroid 727 SPECTRUMTYPE: Centroid
727 FORMULA: C10H13N2OCl 728 FORMULA: C10H13N2OCl
728 INCHIKEY: JXCGFZXSOMJFOA-UHFFFAOYSA-N 729 INCHIKEY: JXCGFZXSOMJFOA-UHFFFAOYSA-N
731 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 732 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
732 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 733 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
733 IONIZATION: ESI+ 734 IONIZATION: ESI+
734 LICENSE: CC BY-NC 735 LICENSE: CC BY-NC
735 COMMENT: 736 COMMENT:
736 COMPOUND_NAME: Chlortoluron
737 RETENTION_TIME: 5.193264 737 RETENTION_TIME: 5.193264
738 PRECURSOR_MZ: 213.0795 738 PRECURSOR_MZ: 213.0795
739 ADDUCT: [M+H]+ 739 ADDUCT: [M+H]+
740 COLLISION_ENERGY: 740 COLLISION_ENERGY:
741 INSTRUMENT_TYPE: LC-ESI-Orbitrap 741 INSTRUMENT_TYPE: LC-ESI-Orbitrap
742 NUM PEAKS: 14 742 NUM PEAKS: 14
743 89.03883 57032.0 743 89.03883 57032.0
744 95.04929 125786.0 744 95.04929 125786.0
745 96.04461 17062.0 745 96.04461 17062.0
746 98.99973 31149.0 746 98.99973 31149.0
747 104.04956 355337.0 747 104.04956 355337.0
748 105.04477 72262.0 748 105.04477 72262.0
749 105.05748 49060.0 749 105.05748 49060.0
750 113.01541 282031.0 750 113.01541 282031.0
751 125.01533 380427.0 751 125.01533 380427.0
752 132.04463 44913.0 752 132.04463 44913.0
753 133.05254 86668.0 753 133.05254 86668.0
754 140.02612 1662428.0 754 140.02612 1662428.0
755 153.02165 91587.0 755 153.02165 91587.0
756 168.02145 83345.0 756 168.02145 83345.0
757 757
758 COMPOUND_NAME: Cycluron
758 SCANNUMBER: 2273 759 SCANNUMBER: 2273
759 IONMODE: Positive 760 IONMODE: Positive
760 SPECTRUMTYPE: Centroid 761 SPECTRUMTYPE: Centroid
761 FORMULA: C11H22N2O 762 FORMULA: C11H22N2O
762 INCHIKEY: DQZCVNGCTZLGAQ-UHFFFAOYSA-N 763 INCHIKEY: DQZCVNGCTZLGAQ-UHFFFAOYSA-N
765 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 766 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
766 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 767 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
767 IONIZATION: ESI+ 768 IONIZATION: ESI+
768 LICENSE: CC BY-NC 769 LICENSE: CC BY-NC
769 COMMENT: 770 COMMENT:
770 COMPOUND_NAME: Cycluron
771 RETENTION_TIME: 5.00998 771 RETENTION_TIME: 5.00998
772 PRECURSOR_MZ: 199.1809 772 PRECURSOR_MZ: 199.1809
773 ADDUCT: [M+H]+ 773 ADDUCT: [M+H]+
774 COLLISION_ENERGY: 774 COLLISION_ENERGY:
775 INSTRUMENT_TYPE: LC-ESI-Orbitrap 775 INSTRUMENT_TYPE: LC-ESI-Orbitrap
776 NUM PEAKS: 4 776 NUM PEAKS: 4
777 89.07108 1303776.0 777 89.07108 1303776.0
778 111.11694 18709.0 778 111.11694 18709.0
779 147.92079 14411.0 779 147.92079 14411.0
780 147.93768 15209.0 780 147.93768 15209.0
781 781
782 COMPOUND_NAME: Diethofencarb
782 SCANNUMBER: 3582 783 SCANNUMBER: 3582
783 IONMODE: Positive 784 IONMODE: Positive
784 SPECTRUMTYPE: Centroid 785 SPECTRUMTYPE: Centroid
785 FORMULA: C14H21NO4 786 FORMULA: C14H21NO4
786 INCHIKEY: LNJNFVJKDJYTEU-UHFFFAOYSA-N 787 INCHIKEY: LNJNFVJKDJYTEU-UHFFFAOYSA-N
789 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 790 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
790 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 791 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
791 IONIZATION: ESI+ 792 IONIZATION: ESI+
792 LICENSE: CC BY-NC 793 LICENSE: CC BY-NC
793 COMMENT: 794 COMMENT:
794 COMPOUND_NAME: Diethofencarb
795 RETENTION_TIME: 6.124817 795 RETENTION_TIME: 6.124817
796 PRECURSOR_MZ: 268.1547 796 PRECURSOR_MZ: 268.1547
797 ADDUCT: [M+H]+ 797 ADDUCT: [M+H]+
798 COLLISION_ENERGY: 798 COLLISION_ENERGY:
799 INSTRUMENT_TYPE: LC-ESI-Orbitrap 799 INSTRUMENT_TYPE: LC-ESI-Orbitrap
800 NUM PEAKS: 7 800 NUM PEAKS: 7
801 152.07103 98482.0 801 152.07103 98482.0
802 180.06563 117586.0 802 180.06563 117586.0
803 180.10194 441784.0 803 180.10194 441784.0
804 198.0762 507187.0 804 198.0762 507187.0
805 208.09682 172166.0 805 208.09682 172166.0
806 226.10776 6612320.0 806 226.10776 6612320.0
807 268.15411 115526.0 807 268.15411 115526.0
808 808
809 COMPOUND_NAME: Diflubenzuron
809 SCANNUMBER: 5619 810 SCANNUMBER: 5619
810 IONMODE: Positive 811 IONMODE: Positive
811 SPECTRUMTYPE: Centroid 812 SPECTRUMTYPE: Centroid
812 FORMULA: C14H9N2O2ClF2 813 FORMULA: C14H9N2O2ClF2
813 INCHIKEY: QQQYTWIFVNKMRW-UHFFFAOYSA-N 814 INCHIKEY: QQQYTWIFVNKMRW-UHFFFAOYSA-N
816 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 817 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
817 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 818 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
818 IONIZATION: ESI+ 819 IONIZATION: ESI+
819 LICENSE: CC BY-NC 820 LICENSE: CC BY-NC
820 COMMENT: 821 COMMENT:
821 COMPOUND_NAME: Diflubenzuron
822 RETENTION_TIME: 6.959446 822 RETENTION_TIME: 6.959446
823 PRECURSOR_MZ: 311.0396 823 PRECURSOR_MZ: 311.0396
824 ADDUCT: [M+H]+ 824 ADDUCT: [M+H]+
825 COLLISION_ENERGY: 825 COLLISION_ENERGY:
826 INSTRUMENT_TYPE: LC-ESI-Orbitrap 826 INSTRUMENT_TYPE: LC-ESI-Orbitrap
827 NUM PEAKS: 3 827 NUM PEAKS: 3
828 141.01498 340685.0 828 141.01498 340685.0
829 158.04167 9035608.0 829 158.04167 9035608.0
830 311.03952 2283440.0 830 311.03952 2283440.0
831 831
832 COMPOUND_NAME: Diuron
832 SCANNUMBER: 3192 833 SCANNUMBER: 3192
833 IONMODE: Positive 834 IONMODE: Positive
834 SPECTRUMTYPE: Centroid 835 SPECTRUMTYPE: Centroid
835 FORMULA: C9H10N2OCl2 836 FORMULA: C9H10N2OCl2
836 INCHIKEY: XMTQQYYKAHVGBJ-UHFFFAOYSA-N 837 INCHIKEY: XMTQQYYKAHVGBJ-UHFFFAOYSA-N
839 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 840 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
840 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 841 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
841 IONIZATION: ESI+ 842 IONIZATION: ESI+
842 LICENSE: CC BY-NC 843 LICENSE: CC BY-NC
843 COMMENT: 844 COMMENT:
844 COMPOUND_NAME: Diuron
845 RETENTION_TIME: 5.711479 845 RETENTION_TIME: 5.711479
846 PRECURSOR_MZ: 233.0248 846 PRECURSOR_MZ: 233.0248
847 ADDUCT: [M+H]+ 847 ADDUCT: [M+H]+
848 COLLISION_ENERGY: 848 COLLISION_ENERGY:
849 INSTRUMENT_TYPE: LC-ESI-Orbitrap 849 INSTRUMENT_TYPE: LC-ESI-Orbitrap
850 NUM PEAKS: 8 850 NUM PEAKS: 8
851 123.99487 30141.0 851 123.99487 30141.0
852 125.00295 82231.0 852 125.00295 82231.0
853 132.96072 233186.0 853 132.96072 233186.0
854 151.03258 25890.0 854 151.03258 25890.0
855 152.99777 66942.0 855 152.99777 66942.0
856 159.97182 940217.0 856 159.97182 940217.0
857 172.96721 73012.0 857 172.96721 73012.0
858 187.96654 38425.0 858 187.96654 38425.0
859 859
860 COMPOUND_NAME: Dioxacarb
860 SCANNUMBER: 1320 861 SCANNUMBER: 1320
861 IONMODE: Positive 862 IONMODE: Positive
862 SPECTRUMTYPE: Centroid 863 SPECTRUMTYPE: Centroid
863 FORMULA: C11H13NO4 864 FORMULA: C11H13NO4
864 INCHIKEY: SDKQRNRRDYRQKY-UHFFFAOYSA-N 865 INCHIKEY: SDKQRNRRDYRQKY-UHFFFAOYSA-N
867 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 868 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
868 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 869 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
869 IONIZATION: ESI+ 870 IONIZATION: ESI+
870 LICENSE: CC BY-NC 871 LICENSE: CC BY-NC
871 COMMENT: 872 COMMENT:
872 COMPOUND_NAME: Dioxacarb
873 RETENTION_TIME: 2.808769 873 RETENTION_TIME: 2.808769
874 PRECURSOR_MZ: 224.092 874 PRECURSOR_MZ: 224.092
875 ADDUCT: [M+H]+ 875 ADDUCT: [M+H]+
876 COLLISION_ENERGY: 876 COLLISION_ENERGY:
877 INSTRUMENT_TYPE: LC-ESI-Orbitrap 877 INSTRUMENT_TYPE: LC-ESI-Orbitrap
878 NUM PEAKS: 6 878 NUM PEAKS: 6
879 95.04929 26554.0 879 95.04929 26554.0
880 123.04434 805609.0 880 123.04434 805609.0
881 162.05486 264649.0 881 162.05486 264649.0
882 167.07042 1519113.0 882 167.07042 1519113.0
883 208.95668 21966.0 883 208.95668 21966.0
884 224.12801 18664.0 884 224.12801 18664.0
885 885
886 COMPOUND_NAME: Bendiocarb
886 SCANNUMBER: 1667 887 SCANNUMBER: 1667
887 IONMODE: Positive 888 IONMODE: Positive
888 SPECTRUMTYPE: Centroid 889 SPECTRUMTYPE: Centroid
889 FORMULA: C11H13NO4 890 FORMULA: C11H13NO4
890 INCHIKEY: XEGGRYVFLWGFHI-UHFFFAOYSA-N 891 INCHIKEY: XEGGRYVFLWGFHI-UHFFFAOYSA-N
893 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 894 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
894 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 895 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
895 IONIZATION: ESI+ 896 IONIZATION: ESI+
896 LICENSE: CC BY-NC 897 LICENSE: CC BY-NC
897 COMMENT: 898 COMMENT:
898 COMPOUND_NAME: Bendiocarb
899 RETENTION_TIME: 4.036841 899 RETENTION_TIME: 4.036841
900 PRECURSOR_MZ: 224.092 900 PRECURSOR_MZ: 224.092
901 ADDUCT: [M+H]+ 901 ADDUCT: [M+H]+
902 COLLISION_ENERGY: 902 COLLISION_ENERGY:
903 INSTRUMENT_TYPE: LC-ESI-Orbitrap 903 INSTRUMENT_TYPE: LC-ESI-Orbitrap
904 NUM PEAKS: 4 904 NUM PEAKS: 4
905 109.02843 576717.0 905 109.02843 576717.0
906 167.07042 2075283.0 906 167.07042 2075283.0
907 224.092 50305.0 907 224.092 50305.0
908 224.12801 22894.0 908 224.12801 22894.0
909 909
910 COMPOUND_NAME: Fenobucarb
910 SCANNUMBER: 2735 911 SCANNUMBER: 2735
911 IONMODE: Positive 912 IONMODE: Positive
912 SPECTRUMTYPE: Centroid 913 SPECTRUMTYPE: Centroid
913 FORMULA: C12H17NO2 914 FORMULA: C12H17NO2
914 INCHIKEY: DIRFUJHNVNOBMY-VIFPVBQESA-N 915 INCHIKEY: DIRFUJHNVNOBMY-VIFPVBQESA-N
917 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 918 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
918 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 919 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
919 IONIZATION: ESI+ 920 IONIZATION: ESI+
920 LICENSE: CC BY-NC 921 LICENSE: CC BY-NC
921 COMMENT: 922 COMMENT:
922 COMPOUND_NAME: Fenobucarb
923 RETENTION_TIME: 5.279047 923 RETENTION_TIME: 5.279047
924 PRECURSOR_MZ: 208.1339 924 PRECURSOR_MZ: 208.1339
925 ADDUCT: [M+H]+ 925 ADDUCT: [M+H]+
926 COLLISION_ENERGY: 926 COLLISION_ENERGY:
927 INSTRUMENT_TYPE: LC-ESI-Orbitrap 927 INSTRUMENT_TYPE: LC-ESI-Orbitrap
928 NUM PEAKS: 5 928 NUM PEAKS: 5
929 95.04929 2304002.0 929 95.04929 2304002.0
930 151.1118 339052.0 930 151.1118 339052.0
931 152.07103 1283617.0 931 152.07103 1283617.0
932 208.13309 261671.0 932 208.13309 261671.0
933 208.15242 67196.0 933 208.15242 67196.0
934 934
935 COMPOUND_NAME: Flufenoxuron
935 SCANNUMBER: 7794 936 SCANNUMBER: 7794
936 IONMODE: Positive 937 IONMODE: Positive
937 SPECTRUMTYPE: Centroid 938 SPECTRUMTYPE: Centroid
938 FORMULA: C21H11N2O3ClF6 939 FORMULA: C21H11N2O3ClF6
939 INCHIKEY: RYLHNOVXKPXDIP-UHFFFAOYSA-N 940 INCHIKEY: RYLHNOVXKPXDIP-UHFFFAOYSA-N
942 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 943 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
943 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 944 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
944 IONIZATION: ESI+ 945 IONIZATION: ESI+
945 LICENSE: CC BY-NC 946 LICENSE: CC BY-NC
946 COMMENT: 947 COMMENT:
947 COMPOUND_NAME: Flufenoxuron
948 RETENTION_TIME: 7.258582 948 RETENTION_TIME: 7.258582
949 PRECURSOR_MZ: 489.044 949 PRECURSOR_MZ: 489.044
950 ADDUCT: [M+H]+ 950 ADDUCT: [M+H]+
951 COLLISION_ENERGY: 951 COLLISION_ENERGY:
952 INSTRUMENT_TYPE: LC-ESI-Orbitrap 952 INSTRUMENT_TYPE: LC-ESI-Orbitrap
953 NUM PEAKS: 9 953 NUM PEAKS: 9
954 140.03102 198040.0 954 140.03102 198040.0
955 141.01498 8731300.0 955 141.01498 8731300.0
956 141.02489 125031.0 956 141.02489 125031.0
957 158.04167 5469943.0 957 158.04167 5469943.0
958 306.03055 226666.0 958 306.03055 226666.0
959 326.76685 460767.0 959 326.76685 460767.0
960 328.76389 301405.0 960 328.76389 301405.0
961 407.68225 401379.0 961 407.68225 401379.0
962 409.68002 103253.0 962 409.68002 103253.0
963 963
964 COMPOUND_NAME: Fluometuron
964 SCANNUMBER: 1879 965 SCANNUMBER: 1879
965 IONMODE: Positive 966 IONMODE: Positive
966 SPECTRUMTYPE: Centroid 967 SPECTRUMTYPE: Centroid
967 FORMULA: C10H11N2OF3 968 FORMULA: C10H11N2OF3
968 INCHIKEY: RZILCCPWPBTYDO-UHFFFAOYSA-N 969 INCHIKEY: RZILCCPWPBTYDO-UHFFFAOYSA-N
971 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 972 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
972 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 973 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
973 IONIZATION: ESI+ 974 IONIZATION: ESI+
974 LICENSE: CC BY-NC 975 LICENSE: CC BY-NC
975 COMMENT: 976 COMMENT:
976 COMPOUND_NAME: Fluometuron
977 RETENTION_TIME: 4.295248 977 RETENTION_TIME: 4.295248
978 PRECURSOR_MZ: 233.0903 978 PRECURSOR_MZ: 233.0903
979 ADDUCT: [M+H]+ 979 ADDUCT: [M+H]+
980 COLLISION_ENERGY: 980 COLLISION_ENERGY:
981 INSTRUMENT_TYPE: LC-ESI-Orbitrap 981 INSTRUMENT_TYPE: LC-ESI-Orbitrap
982 NUM PEAKS: 14 982 NUM PEAKS: 14
983 133.02617 72647.0 983 133.02617 72647.0
984 140.03056 412576.0 984 140.03056 412576.0
985 141.02579 30382.0 985 141.02579 30382.0
986 145.02599 1001995.0 986 145.02599 1001995.0
987 148.03093 43335.0 987 148.03093 43335.0
988 160.03375 16242.0 988 160.03375 16242.0
989 160.037 1435798.0 989 160.037 1435798.0
990 163.0365 19807.0 990 163.0365 19807.0
991 168.02554 576288.0 991 168.02554 576288.0
992 173.03194 272722.0 992 173.03194 272722.0
993 173.50755 34131.0 993 173.50755 34131.0
994 178.04784 113811.0 994 178.04784 113811.0
995 188.03226 109696.0 995 188.03226 109696.0
996 192.06305 82452.0 996 192.06305 82452.0
997 997
998 COMPOUND_NAME: Forchlorfenuron
998 SCANNUMBER: 3521 999 SCANNUMBER: 3521
999 IONMODE: Positive 1000 IONMODE: Positive
1000 SPECTRUMTYPE: Centroid 1001 SPECTRUMTYPE: Centroid
1001 FORMULA: C12H10N3OCl 1002 FORMULA: C12H10N3OCl
1002 INCHIKEY: GPXLRLUVLMHHIK-UHFFFAOYSA-N 1003 INCHIKEY: GPXLRLUVLMHHIK-UHFFFAOYSA-N
1005 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1006 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1006 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1007 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1007 IONIZATION: ESI+ 1008 IONIZATION: ESI+
1008 LICENSE: CC BY-NC 1009 LICENSE: CC BY-NC
1009 COMMENT: 1010 COMMENT:
1010 COMPOUND_NAME: Forchlorfenuron
1011 RETENTION_TIME: 6.068144 1011 RETENTION_TIME: 6.068144
1012 PRECURSOR_MZ: 248.0593 1012 PRECURSOR_MZ: 248.0593
1013 ADDUCT: [M+H]+ 1013 ADDUCT: [M+H]+
1014 COLLISION_ENERGY: 1014 COLLISION_ENERGY:
1015 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1015 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1016 NUM PEAKS: 6 1016 NUM PEAKS: 6
1017 93.04498 1144138.0 1017 93.04498 1144138.0
1018 94.06544 222850.0 1018 94.06544 222850.0
1019 111.05567 15214406.0 1019 111.05567 15214406.0
1020 129.02182 20609304.0 1020 129.02182 20609304.0
1021 137.03458 1954463.0 1021 137.03458 1954463.0
1022 155.00107 2962225.0 1022 155.00107 2962225.0
1023 1023
1024 COMPOUND_NAME: 3-Hydroxycarbofuran
1024 SCANNUMBER: 1109 1025 SCANNUMBER: 1109
1025 IONMODE: Positive 1026 IONMODE: Positive
1026 SPECTRUMTYPE: Centroid 1027 SPECTRUMTYPE: Centroid
1027 FORMULA: C12H15NO4 1028 FORMULA: C12H15NO4
1028 INCHIKEY: RHSUJRQZTQNSLL-JTQLQIEISA-N 1029 INCHIKEY: RHSUJRQZTQNSLL-JTQLQIEISA-N
1031 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1032 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1032 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1033 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1033 IONIZATION: ESI+ 1034 IONIZATION: ESI+
1034 LICENSE: CC BY-NC 1035 LICENSE: CC BY-NC
1035 COMMENT: 1036 COMMENT:
1036 COMPOUND_NAME: 3-Hydroxycarbofuran
1037 RETENTION_TIME: 2.534817 1037 RETENTION_TIME: 2.534817
1038 PRECURSOR_MZ: 238.1075 1038 PRECURSOR_MZ: 238.1075
1039 ADDUCT: [M+H]+ 1039 ADDUCT: [M+H]+
1040 COLLISION_ENERGY: 1040 COLLISION_ENERGY:
1041 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1041 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1042 NUM PEAKS: 7 1042 NUM PEAKS: 7
1043 135.08051 61121.0 1043 135.08051 61121.0
1044 163.07562 1270756.0 1044 163.07562 1270756.0
1045 181.08611 3459316.0 1045 181.08611 3459316.0
1046 207.06541 67306.0 1046 207.06541 67306.0
1047 208.95668 38515.0 1047 208.95668 38515.0
1048 220.09669 446913.0 1048 220.09669 446913.0
1049 238.10802 398788.0 1049 238.10802 398788.0
1050 1050
1051 COMPOUND_NAME: Indoxacarb
1051 SCANNUMBER: 7519 1052 SCANNUMBER: 7519
1052 IONMODE: Positive 1053 IONMODE: Positive
1053 SPECTRUMTYPE: Centroid 1054 SPECTRUMTYPE: Centroid
1054 FORMULA: C22H17N3O7ClF3 1055 FORMULA: C22H17N3O7ClF3
1055 INCHIKEY: VBCVPMMZEGZULK-NRFANRHFSA-N 1056 INCHIKEY: VBCVPMMZEGZULK-NRFANRHFSA-N
1058 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1059 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1059 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1060 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1060 IONIZATION: ESI+ 1061 IONIZATION: ESI+
1061 LICENSE: CC BY-NC 1062 LICENSE: CC BY-NC
1062 COMMENT: 1063 COMMENT:
1063 COMPOUND_NAME: Indoxacarb
1064 RETENTION_TIME: 7.23968 1064 RETENTION_TIME: 7.23968
1065 PRECURSOR_MZ: 528.0795 1065 PRECURSOR_MZ: 528.0795
1066 ADDUCT: [M+H]+ 1066 ADDUCT: [M+H]+
1067 COLLISION_ENERGY: 1067 COLLISION_ENERGY:
1068 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1068 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1069 NUM PEAKS: 38 1069 NUM PEAKS: 38
1070 104.04956 303700.0 1070 104.04956 303700.0
1071 127.04175 99545.0 1071 127.04175 99545.0
1072 128.06201 117126.0 1072 128.06201 117126.0
1073 132.04463 290691.0 1073 132.04463 290691.0
1074 134.0237 264912.0 1074 134.0237 264912.0
1075 137.0152 94534.0 1075 137.0152 94534.0
1076 142.06526 75186.0 1076 142.06526 75186.0
1077 149.01559 214826.0 1077 149.01559 214826.0
1078 150.0106 1405054.0 1078 150.0106 1405054.0
1079 155.06065 232073.0 1079 155.06065 232073.0
1080 160.05058 254333.0 1080 160.05058 254333.0
1081 162.01057 1521152.0 1081 162.01057 1521152.0
1082 163.01862 86648.0 1082 163.01862 86648.0
1083 163.03091 132653.0 1083 163.03091 132653.0
1084 164.02652 208730.0 1084 164.02652 208730.0
1085 165.03412 90438.0 1085 165.03412 90438.0
1086 167.0258 357529.0 1086 167.0258 357529.0
1087 168.02145 1690027.0 1087 168.02145 1690027.0
1088 174.99464 101678.0 1088 174.99464 101678.0
1089 177.01054 92638.0 1089 177.01054 92638.0
1090 177.03394 231314.0 1090 177.03394 231314.0
1091 179.02611 358184.0 1091 179.02611 358184.0
1092 180.02089 413839.0 1092 180.02089 413839.0
1093 182.03682 119810.0 1093 182.03682 119810.0
1094 189.02151 643960.0 1094 189.02151 643960.0
1095 190.00526 1446936.0 1095 190.00526 1446936.0
1096 190.04744 486518.0 1096 190.04744 486518.0
1097 194.03688 93119.0 1097 194.03688 93119.0
1098 195.02061 551503.0 1098 195.02061 551503.0
1099 203.01863 7362278.0 1099 203.01863 7362278.0
1100 204.00897 308332.0 1100 204.00897 308332.0
1101 207.02065 269934.0 1101 207.02065 269934.0
1102 208.01628 221573.0 1102 208.01628 221573.0
1103 215.04312 81774.0 1103 215.04312 81774.0
1104 217.01668 489943.0 1104 217.01668 489943.0
1105 218.04218 536326.0 1105 218.04218 536326.0
1106 219.03232 457473.0 1106 219.03232 457473.0
1107 223.01553 87858.0 1107 223.01553 87858.0
1108 1108
1109 COMPOUND_NAME: Iprovalicarb
1109 SCANNUMBER: 3798 1110 SCANNUMBER: 3798
1110 IONMODE: Positive 1111 IONMODE: Positive
1111 SPECTRUMTYPE: Centroid 1112 SPECTRUMTYPE: Centroid
1112 FORMULA: C18H28N2O3 1113 FORMULA: C18H28N2O3
1113 INCHIKEY: NWUWYYSKZYIQAE-WMCAAGNKSA-N 1114 INCHIKEY: NWUWYYSKZYIQAE-WMCAAGNKSA-N
1116 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1117 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1117 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1118 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1118 IONIZATION: ESI+ 1119 IONIZATION: ESI+
1119 LICENSE: CC BY-NC 1120 LICENSE: CC BY-NC
1120 COMMENT: 1121 COMMENT:
1121 COMPOUND_NAME: Iprovalicarb
1122 RETENTION_TIME: 6.291288 1122 RETENTION_TIME: 6.291288
1123 PRECURSOR_MZ: 321.218 1123 PRECURSOR_MZ: 321.218
1124 ADDUCT: [M+H]+ 1124 ADDUCT: [M+H]+
1125 COLLISION_ENERGY: 1125 COLLISION_ENERGY:
1126 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1126 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1127 NUM PEAKS: 9 1127 NUM PEAKS: 9
1128 116.07085 2061421.0 1128 116.07085 2061421.0
1129 117.10262 213026.0 1129 117.10262 213026.0
1130 119.0857 8088768.0 1130 119.0857 8088768.0
1131 144.06569 976637.0 1131 144.06569 976637.0
1132 158.11795 349762.0 1132 158.11795 349762.0
1133 161.09248 110448.0 1133 161.09248 110448.0
1134 186.11298 1809182.0 1134 186.11298 1809182.0
1135 203.13902 3619220.0 1135 203.13902 3619220.0
1136 321.21719 658523.0 1136 321.21719 658523.0
1137 1137
1138 COMPOUND_NAME: Isoproturon
1138 SCANNUMBER: 2221 1139 SCANNUMBER: 2221
1139 IONMODE: Positive 1140 IONMODE: Positive
1140 SPECTRUMTYPE: Centroid 1141 SPECTRUMTYPE: Centroid
1141 FORMULA: C12H18N2O 1142 FORMULA: C12H18N2O
1142 INCHIKEY: PUIYMUZLKQOUOZ-UHFFFAOYSA-N 1143 INCHIKEY: PUIYMUZLKQOUOZ-UHFFFAOYSA-N
1145 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1146 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1146 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1147 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1147 IONIZATION: ESI+ 1148 IONIZATION: ESI+
1148 LICENSE: CC BY-NC 1149 LICENSE: CC BY-NC
1149 COMMENT: 1150 COMMENT:
1150 COMPOUND_NAME: Isoproturon
1151 RETENTION_TIME: 4.953308 1151 RETENTION_TIME: 4.953308
1152 PRECURSOR_MZ: 207.1494 1152 PRECURSOR_MZ: 207.1494
1153 ADDUCT: [M+H]+ 1153 ADDUCT: [M+H]+
1154 COLLISION_ENERGY: 1154 COLLISION_ENERGY:
1155 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1155 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1156 NUM PEAKS: 27 1156 NUM PEAKS: 27
1157 91.05442 804905.0 1157 91.05442 804905.0
1158 92.04957 254047.0 1158 92.04957 254047.0
1159 93.0575 33128.0 1159 93.0575 33128.0
1160 93.07003 116103.0 1160 93.07003 116103.0
1161 94.06519 63492.0 1161 94.06519 63492.0
1162 95.04929 164116.0 1162 95.04929 164116.0
1163 103.05439 51947.0 1163 103.05439 51947.0
1164 104.0621 43995.0 1164 104.0621 43995.0
1165 105.04477 78368.0 1165 105.04477 78368.0
1166 105.06991 101627.0 1166 105.06991 101627.0
1167 106.06517 86652.0 1167 106.06517 86652.0
1168 107.08415 19657.0 1168 107.08415 19657.0
1169 107.08563 575392.0 1169 107.08563 575392.0
1170 108.08108 26529.0 1170 108.08108 26529.0
1171 109.0651 34575.0 1171 109.0651 34575.0
1172 115.05431 109513.0 1172 115.05431 109513.0
1173 117.06998 312366.0 1173 117.06998 312366.0
1174 118.06519 123299.0 1174 118.06519 123299.0
1175 119.0606 36796.0 1175 119.0606 36796.0
1176 119.07315 606574.0 1176 119.07315 606574.0
1177 120.04464 242145.0 1177 120.04464 242145.0
1178 132.08089 72884.0 1178 132.08089 72884.0
1179 134.0966 1730390.0 1179 134.0966 1730390.0
1180 137.09615 58215.0 1180 137.09615 58215.0
1181 147.0919 129941.0 1181 147.0919 129941.0
1182 162.09142 42617.0 1182 162.09142 42617.0
1183 165.10242 74899.0 1183 165.10242 74899.0
1184 1184
1185 COMPOUND_NAME: Linuron
1185 SCANNUMBER: 3991 1186 SCANNUMBER: 3991
1186 IONMODE: Positive 1187 IONMODE: Positive
1187 SPECTRUMTYPE: Centroid 1188 SPECTRUMTYPE: Centroid
1188 FORMULA: C9H10N2O2Cl2 1189 FORMULA: C9H10N2O2Cl2
1189 INCHIKEY: XKJMBINCVNINCA-UHFFFAOYSA-N 1190 INCHIKEY: XKJMBINCVNINCA-UHFFFAOYSA-N
1192 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1193 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1193 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1194 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1194 IONIZATION: ESI+ 1195 IONIZATION: ESI+
1195 LICENSE: CC BY-NC 1196 LICENSE: CC BY-NC
1196 COMMENT: 1197 COMMENT:
1197 COMPOUND_NAME: Linuron
1198 RETENTION_TIME: 6.428301 1198 RETENTION_TIME: 6.428301
1199 PRECURSOR_MZ: 249.0202 1199 PRECURSOR_MZ: 249.0202
1200 ADDUCT: [M+H]+ 1200 ADDUCT: [M+H]+
1201 COLLISION_ENERGY: 1201 COLLISION_ENERGY:
1202 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1202 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1203 NUM PEAKS: 17 1203 NUM PEAKS: 17
1204 123.99524 160993.0 1204 123.99524 160993.0
1205 125.00295 934482.0 1205 125.00295 934482.0
1206 126.01085 53171.0 1206 126.01085 53171.0
1207 127.0187 34132.0 1207 127.0187 34132.0
1208 132.96072 2098030.0 1208 132.96072 2098030.0
1209 133.96875 42332.0 1209 133.96875 42332.0
1210 142.00574 58394.0 1210 142.00574 58394.0
1211 153.02165 907640.0 1211 153.02165 907640.0
1212 154.02942 31975.0 1212 154.02942 31975.0
1213 159.97182 1453641.0 1213 159.97182 1453641.0
1214 160.97951 1564652.0 1214 160.97951 1564652.0
1215 165.02161 76894.0 1215 165.02161 76894.0
1216 167.0009 34764.0 1216 167.0009 34764.0
1217 173.98759 32777.0 1217 173.98759 32777.0
1218 181.0168 457538.0 1218 181.0168 457538.0
1219 182.02429 570846.0 1219 182.02429 570846.0
1220 216.99352 182540.0 1220 216.99352 182540.0
1221 1221
1222 COMPOUND_NAME: Metobromuron
1222 SCANNUMBER: 2948 1223 SCANNUMBER: 2948
1223 IONMODE: Positive 1224 IONMODE: Positive
1224 SPECTRUMTYPE: Centroid 1225 SPECTRUMTYPE: Centroid
1225 FORMULA: C9H11N2O2Br 1226 FORMULA: C9H11N2O2Br
1226 INCHIKEY: WLFDQEVORAMCIM-UHFFFAOYSA-N 1227 INCHIKEY: WLFDQEVORAMCIM-UHFFFAOYSA-N
1229 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1230 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1230 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1231 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1231 IONIZATION: ESI+ 1232 IONIZATION: ESI+
1232 LICENSE: CC BY-NC 1233 LICENSE: CC BY-NC
1233 COMMENT: 1234 COMMENT:
1234 COMPOUND_NAME: Metobromuron
1235 RETENTION_TIME: 5.555997 1235 RETENTION_TIME: 5.555997
1236 PRECURSOR_MZ: 259.0081 1236 PRECURSOR_MZ: 259.0081
1237 ADDUCT: [M+H]+ 1237 ADDUCT: [M+H]+
1238 COLLISION_ENERGY: 1238 COLLISION_ENERGY:
1239 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1239 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1240 NUM PEAKS: 15 1240 NUM PEAKS: 15
1241 90.03403 60649.0 1241 90.03403 60649.0
1242 91.04183 2389714.0 1242 91.04183 2389714.0
1243 92.04957 214805.0 1243 92.04957 214805.0
1244 93.0575 47461.0 1244 93.0575 47461.0
1245 110.06014 105724.0 1245 110.06014 105724.0
1246 119.0606 1438162.0 1246 119.0606 1438162.0
1247 120.06829 52547.0 1247 120.06829 52547.0
1248 131.06062 84354.0 1248 131.06062 84354.0
1249 142.94916 1281698.0 1249 142.94916 1281698.0
1250 147.05553 745419.0 1250 147.05553 745419.0
1251 148.06332 717928.0 1251 148.06332 717928.0
1252 169.95995 3654354.0 1252 169.95995 3654354.0
1253 170.96819 2866842.0 1253 170.96819 2866842.0
1254 183.97557 70285.0 1254 183.97557 70285.0
1255 226.98169 352678.0 1255 226.98169 352678.0
1256 1256
1257 COMPOUND_NAME: Monolinuron
1257 SCANNUMBER: 2345 1258 SCANNUMBER: 2345
1258 IONMODE: Positive 1259 IONMODE: Positive
1259 SPECTRUMTYPE: Centroid 1260 SPECTRUMTYPE: Centroid
1260 FORMULA: C9H11N2O2Cl 1261 FORMULA: C9H11N2O2Cl
1261 INCHIKEY: LKJPSUCKSLORMF-UHFFFAOYSA-N 1262 INCHIKEY: LKJPSUCKSLORMF-UHFFFAOYSA-N
1264 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1265 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1265 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1266 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1266 IONIZATION: ESI+ 1267 IONIZATION: ESI+
1267 LICENSE: CC BY-NC 1268 LICENSE: CC BY-NC
1268 COMMENT: 1269 COMMENT:
1269 COMPOUND_NAME: Monolinuron
1270 RETENTION_TIME: 5.086284 1270 RETENTION_TIME: 5.086284
1271 PRECURSOR_MZ: 215.0587 1271 PRECURSOR_MZ: 215.0587
1272 ADDUCT: [M+H]+ 1272 ADDUCT: [M+H]+
1273 COLLISION_ENERGY: 1273 COLLISION_ENERGY:
1274 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1274 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1275 NUM PEAKS: 16 1275 NUM PEAKS: 16
1276 90.03403 245033.0 1276 90.03403 245033.0
1277 91.04183 266487.0 1277 91.04183 266487.0
1278 92.0498 149734.0 1278 92.0498 149734.0
1279 93.0575 65470.0 1279 93.0575 65470.0
1280 98.99973 5081895.0 1280 98.99973 5081895.0
1281 100.00744 171810.0 1281 100.00744 171810.0
1282 119.0606 1725493.0 1282 119.0606 1725493.0
1283 120.06829 76212.0 1283 120.06829 76212.0
1284 126.01085 4292995.0 1284 126.01085 4292995.0
1285 127.01831 4179362.0 1285 127.01831 4179362.0
1286 131.06062 91755.0 1286 131.06062 91755.0
1287 140.02657 95768.0 1287 140.02657 95768.0
1288 141.02174 52283.0 1288 141.02174 52283.0
1289 147.05553 873918.0 1289 147.05553 873918.0
1290 148.06332 1071865.0 1290 148.06332 1071865.0
1291 183.03224 448058.0 1291 183.03224 448058.0
1292 1292
1293 COMPOUND_NAME: Fenoxycarb
1293 SCANNUMBER: 6056 1294 SCANNUMBER: 6056
1294 IONMODE: Positive 1295 IONMODE: Positive
1295 SPECTRUMTYPE: Centroid 1296 SPECTRUMTYPE: Centroid
1296 FORMULA: C17H19NO4 1297 FORMULA: C17H19NO4
1297 INCHIKEY: HJUFTIJOISQSKQ-UHFFFAOYSA-N 1298 INCHIKEY: HJUFTIJOISQSKQ-UHFFFAOYSA-N
1300 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1301 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1301 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1302 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1302 IONIZATION: ESI+ 1303 IONIZATION: ESI+
1303 LICENSE: CC BY-NC 1304 LICENSE: CC BY-NC
1304 COMMENT: 1305 COMMENT:
1305 COMPOUND_NAME: Fenoxycarb
1306 RETENTION_TIME: 7.007411 1306 RETENTION_TIME: 7.007411
1307 PRECURSOR_MZ: 302.1392 1307 PRECURSOR_MZ: 302.1392
1308 ADDUCT: [M+H]+ 1308 ADDUCT: [M+H]+
1309 COLLISION_ENERGY: 1309 COLLISION_ENERGY:
1310 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1310 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1311 NUM PEAKS: 4 1311 NUM PEAKS: 4
1312 88.03963 3398675.0 1312 88.03963 3398675.0
1313 116.07085 7870537.0 1313 116.07085 7870537.0
1314 256.09756 3714539.0 1314 256.09756 3714539.0
1315 302.13986 4154405.0 1315 302.13986 4154405.0
1316 1316
1317 COMPOUND_NAME: Fenuron
1317 SCANNUMBER: 1173 1318 SCANNUMBER: 1173
1318 IONMODE: Positive 1319 IONMODE: Positive
1319 SPECTRUMTYPE: Centroid 1320 SPECTRUMTYPE: Centroid
1320 FORMULA: C9H12N2O 1321 FORMULA: C9H12N2O
1321 INCHIKEY: XXOYNJXVWVNOOJ-UHFFFAOYSA-N 1322 INCHIKEY: XXOYNJXVWVNOOJ-UHFFFAOYSA-N
1324 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1325 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1325 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1326 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1326 IONIZATION: ESI+ 1327 IONIZATION: ESI+
1327 LICENSE: CC BY-NC 1328 LICENSE: CC BY-NC
1328 COMMENT: 1329 COMMENT:
1329 COMPOUND_NAME: Fenuron
1330 RETENTION_TIME: 2.603287 1330 RETENTION_TIME: 2.603287
1331 PRECURSOR_MZ: 165.1026 1331 PRECURSOR_MZ: 165.1026
1332 ADDUCT: [M+H]+ 1332 ADDUCT: [M+H]+
1333 COLLISION_ENERGY: 1333 COLLISION_ENERGY:
1334 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1334 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1335 NUM PEAKS: 8 1335 NUM PEAKS: 8
1336 90.94795 13666.0 1336 90.94795 13666.0
1337 92.04957 465012.0 1337 92.04957 465012.0
1338 93.0575 10288.0 1338 93.0575 10288.0
1339 95.0478 10698.0 1339 95.0478 10698.0
1340 95.04929 620773.0 1340 95.04929 620773.0
1341 104.96333 7099.0 1341 104.96333 7099.0
1342 105.04477 391134.0 1342 105.04477 391134.0
1343 120.04464 89335.0 1343 120.04464 89335.0
1344 1344
1345 COMPOUND_NAME: Isoprocarb
1345 SCANNUMBER: 2001 1346 SCANNUMBER: 2001
1346 IONMODE: Positive 1347 IONMODE: Positive
1347 SPECTRUMTYPE: Centroid 1348 SPECTRUMTYPE: Centroid
1348 FORMULA: C11H15NO2 1349 FORMULA: C11H15NO2
1349 INCHIKEY: QBSJMKIUCUGGNG-UHFFFAOYSA-N 1350 INCHIKEY: QBSJMKIUCUGGNG-UHFFFAOYSA-N
1352 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1353 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1353 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1354 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1354 IONIZATION: ESI+ 1355 IONIZATION: ESI+
1355 LICENSE: CC BY-NC 1356 LICENSE: CC BY-NC
1356 COMMENT: 1357 COMMENT:
1357 COMPOUND_NAME: Isoprocarb
1358 RETENTION_TIME: 4.552796 1358 RETENTION_TIME: 4.552796
1359 PRECURSOR_MZ: 194.1181 1359 PRECURSOR_MZ: 194.1181
1360 ADDUCT: [M+H]+ 1360 ADDUCT: [M+H]+
1361 COLLISION_ENERGY: 1361 COLLISION_ENERGY:
1362 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1362 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1363 NUM PEAKS: 4 1363 NUM PEAKS: 4
1364 95.04929 1741248.0 1364 95.04929 1741248.0
1365 137.09615 1255669.0 1365 137.09615 1255669.0
1366 152.07103 658146.0 1366 152.07103 658146.0
1367 194.11743 393850.0 1367 194.11743 393850.0
1368 1368
1369 COMPOUND_NAME: Pyraclostrobin
1369 SCANNUMBER: 8910 1370 SCANNUMBER: 8910
1370 IONMODE: Positive 1371 IONMODE: Positive
1371 SPECTRUMTYPE: Centroid 1372 SPECTRUMTYPE: Centroid
1372 FORMULA: C19H18N3O4Cl 1373 FORMULA: C19H18N3O4Cl
1373 INCHIKEY: HZRSNVGNWUDEFX-UHFFFAOYSA-N 1374 INCHIKEY: HZRSNVGNWUDEFX-UHFFFAOYSA-N
1376 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1377 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1377 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1378 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1378 IONIZATION: ESI+ 1379 IONIZATION: ESI+
1379 LICENSE: CC BY-NC 1380 LICENSE: CC BY-NC
1380 COMMENT: 1381 COMMENT:
1381 COMPOUND_NAME: Pyraclostrobin
1382 RETENTION_TIME: 7.421628 1382 RETENTION_TIME: 7.421628
1383 PRECURSOR_MZ: 388.107 1383 PRECURSOR_MZ: 388.107
1384 ADDUCT: [M+H]+ 1384 ADDUCT: [M+H]+
1385 COLLISION_ENERGY: 1385 COLLISION_ENERGY:
1386 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1386 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1387 NUM PEAKS: 11 1387 NUM PEAKS: 11
1388 162.0554 983545.0 1388 162.0554 983545.0
1389 163.06332 1950324.0 1389 163.06332 1950324.0
1390 164.07108 4818863.0 1390 164.07108 4818863.0
1391 194.08186 23217608.0 1391 194.08186 23217608.0
1392 296.05423 282175.0 1392 296.05423 282175.0
1393 296.05969 5986147.0 1393 296.05969 5986147.0
1394 324.05402 1024635.0 1394 324.05402 1024635.0
1395 356.07611 701579.0 1395 356.07611 701579.0
1396 356.08151 2958382.0 1396 356.08151 2958382.0
1397 357.08807 317478.0 1397 357.08807 317478.0
1398 388.10776 6476718.0 1398 388.10776 6476718.0
1399 1399
1400 COMPOUND_NAME: Siduron_1
1400 SCANNUMBER: 3358 1401 SCANNUMBER: 3358
1401 IONMODE: Positive 1402 IONMODE: Positive
1402 SPECTRUMTYPE: Centroid 1403 SPECTRUMTYPE: Centroid
1403 FORMULA: C14H20N2O 1404 FORMULA: C14H20N2O
1404 INCHIKEY: JXVIIQLNUPXOII-UHFFFAOYSA-N 1405 INCHIKEY: JXVIIQLNUPXOII-UHFFFAOYSA-N
1407 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1408 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1408 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1409 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1409 IONIZATION: ESI+ 1410 IONIZATION: ESI+
1410 LICENSE: CC BY-NC 1411 LICENSE: CC BY-NC
1411 COMMENT: 1412 COMMENT:
1412 COMPOUND_NAME: Siduron_1
1413 RETENTION_TIME: 5.922128 1413 RETENTION_TIME: 5.922128
1414 PRECURSOR_MZ: 233.1652 1414 PRECURSOR_MZ: 233.1652
1415 ADDUCT: [M+H]+ 1415 ADDUCT: [M+H]+
1416 COLLISION_ENERGY: 1416 COLLISION_ENERGY:
1417 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1417 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1418 NUM PEAKS: 8 1418 NUM PEAKS: 8
1419 92.0498 933541.0 1419 92.0498 933541.0
1420 93.0575 170423.0 1420 93.0575 170423.0
1421 94.06544 14211722.0 1421 94.06544 14211722.0
1422 95.04929 2073643.0 1422 95.04929 2073643.0
1423 97.10134 599721.0 1423 97.10134 599721.0
1424 105.04506 1075144.0 1424 105.04506 1075144.0
1425 120.04464 1602718.0 1425 120.04464 1602718.0
1426 137.07117 1760320.0 1426 137.07117 1760320.0
1427 1427
1428 COMPOUND_NAME: Siduron_2
1428 SCANNUMBER: 3451 1429 SCANNUMBER: 3451
1429 IONMODE: Positive 1430 IONMODE: Positive
1430 SPECTRUMTYPE: Centroid 1431 SPECTRUMTYPE: Centroid
1431 FORMULA: C14H20N2O 1432 FORMULA: C14H20N2O
1432 INCHIKEY: JXVIIQLNUPXOII-UHFFFAOYSA-N 1433 INCHIKEY: JXVIIQLNUPXOII-UHFFFAOYSA-N
1435 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1436 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1436 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1437 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1437 IONIZATION: ESI+ 1438 IONIZATION: ESI+
1438 LICENSE: CC BY-NC 1439 LICENSE: CC BY-NC
1439 COMMENT: 1440 COMMENT:
1440 COMPOUND_NAME: Siduron_2
1441 RETENTION_TIME: 6.048454 1441 RETENTION_TIME: 6.048454
1442 PRECURSOR_MZ: 233.1654 1442 PRECURSOR_MZ: 233.1654
1443 ADDUCT: [M+H]+ 1443 ADDUCT: [M+H]+
1444 COLLISION_ENERGY: 1444 COLLISION_ENERGY:
1445 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1445 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1446 NUM PEAKS: 8 1446 NUM PEAKS: 8
1447 92.04957 227079.0 1447 92.04957 227079.0
1448 93.0575 48287.0 1448 93.0575 48287.0
1449 94.06519 3308508.0 1449 94.06519 3308508.0
1450 95.04929 491391.0 1450 95.04929 491391.0
1451 97.10134 147324.0 1451 97.10134 147324.0
1452 105.04477 331107.0 1452 105.04477 331107.0
1453 120.04464 414038.0 1453 120.04464 414038.0
1454 137.07117 494688.0 1454 137.07117 494688.0
1455 1455
1456 COMPOUND_NAME: Thiobencarb
1456 SCANNUMBER: 6489 1457 SCANNUMBER: 6489
1457 IONMODE: Positive 1458 IONMODE: Positive
1458 SPECTRUMTYPE: Centroid 1459 SPECTRUMTYPE: Centroid
1459 FORMULA: C12H16NOClS 1460 FORMULA: C12H16NOClS
1460 INCHIKEY: QHTQREMOGMZHJV-UHFFFAOYSA-N 1461 INCHIKEY: QHTQREMOGMZHJV-UHFFFAOYSA-N
1463 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1464 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1464 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1465 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1465 IONIZATION: ESI+ 1466 IONIZATION: ESI+
1466 LICENSE: CC BY-NC 1467 LICENSE: CC BY-NC
1467 COMMENT: 1468 COMMENT:
1468 COMPOUND_NAME: Thiobencarb
1469 RETENTION_TIME: 7.094566 1469 RETENTION_TIME: 7.094566
1470 PRECURSOR_MZ: 258.0717 1470 PRECURSOR_MZ: 258.0717
1471 ADDUCT: [M+H]+ 1471 ADDUCT: [M+H]+
1472 COLLISION_ENERGY: 1472 COLLISION_ENERGY:
1473 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1473 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1474 NUM PEAKS: 3 1474 NUM PEAKS: 3
1475 89.03883 1114558.0 1475 89.03883 1114558.0
1476 98.99973 585236.0 1476 98.99973 585236.0
1477 125.01533 28327212.0 1477 125.01533 28327212.0
1478 1478
1479 COMPOUND_NAME: Triflumuron
1479 SCANNUMBER: 5946 1480 SCANNUMBER: 5946
1480 IONMODE: Positive 1481 IONMODE: Positive
1481 SPECTRUMTYPE: Centroid 1482 SPECTRUMTYPE: Centroid
1482 FORMULA: C15H10N2O3ClF3 1483 FORMULA: C15H10N2O3ClF3
1483 INCHIKEY: XAIPTRIXGHTTNT-UHFFFAOYSA-N 1484 INCHIKEY: XAIPTRIXGHTTNT-UHFFFAOYSA-N
1486 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1487 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1487 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1488 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1488 IONIZATION: ESI+ 1489 IONIZATION: ESI+
1489 LICENSE: CC BY-NC 1490 LICENSE: CC BY-NC
1490 COMMENT: 1491 COMMENT:
1491 COMPOUND_NAME: Triflumuron
1492 RETENTION_TIME: 6.978649 1492 RETENTION_TIME: 6.978649
1493 PRECURSOR_MZ: 359.0412 1493 PRECURSOR_MZ: 359.0412
1494 ADDUCT: [M+H]+ 1494 ADDUCT: [M+H]+
1495 COLLISION_ENERGY: 1495 COLLISION_ENERGY:
1496 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1496 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1497 NUM PEAKS: 7 1497 NUM PEAKS: 7
1498 113.01541 658622.0 1498 113.01541 658622.0
1499 129.01042 138249.0 1499 129.01042 138249.0
1500 138.011 140957.0 1500 138.011 140957.0
1501 138.99484 9851099.0 1501 138.99484 9851099.0
1502 139.00452 474854.0 1502 139.00452 474854.0
1503 156.02116 3353307.0 1503 156.02116 3353307.0
1504 178.04784 200379.0 1504 178.04784 200379.0
1505 1505
1506 COMPOUND_NAME: Propham
1506 SCANNUMBER: 3629 1507 SCANNUMBER: 3629
1507 IONMODE: Positive 1508 IONMODE: Positive
1508 SPECTRUMTYPE: Centroid 1509 SPECTRUMTYPE: Centroid
1509 FORMULA: C10H13NO2 1510 FORMULA: C10H13NO2
1510 INCHIKEY: VXPLXMJHHKHSOA-UHFFFAOYSA-N 1511 INCHIKEY: VXPLXMJHHKHSOA-UHFFFAOYSA-N
1513 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1514 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1514 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1515 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1515 IONIZATION: ESI+ 1516 IONIZATION: ESI+
1516 LICENSE: CC BY-NC 1517 LICENSE: CC BY-NC
1517 COMMENT: 1518 COMMENT:
1518 COMPOUND_NAME: Propham
1519 RETENTION_TIME: 6.134321 1519 RETENTION_TIME: 6.134321
1520 PRECURSOR_MZ: 180.1022 1520 PRECURSOR_MZ: 180.1022
1521 ADDUCT: [M+H]+ 1521 ADDUCT: [M+H]+
1522 COLLISION_ENERGY: 1522 COLLISION_ENERGY:
1523 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1523 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1524 NUM PEAKS: 13 1524 NUM PEAKS: 13
1525 91.05442 8291.0 1525 91.05442 8291.0
1526 93.0575 2806.0 1526 93.0575 2806.0
1527 95.04929 8647.0 1527 95.04929 8647.0
1528 96.04461 67785.0 1528 96.04461 67785.0
1529 97.02845 206258.0 1529 97.02845 206258.0
1530 105.0335 4841.0 1530 105.0335 4841.0
1531 105.04477 6538.0 1531 105.04477 6538.0
1532 106.02882 185730.0 1532 106.02882 185730.0
1533 109.02843 2611.0 1533 109.02843 2611.0
1534 117.0574 2236.0 1534 117.0574 2236.0
1535 124.03935 187312.0 1535 124.03935 187312.0
1536 134.0237 14609.0 1536 134.0237 14609.0
1537 152.0343 3135.0 1537 152.0343 3135.0
1538 1538
1539 COMPOUND_NAME: Propoxur
1539 SCANNUMBER: 1562 1540 SCANNUMBER: 1562
1540 IONMODE: Positive 1541 IONMODE: Positive
1541 SPECTRUMTYPE: Centroid 1542 SPECTRUMTYPE: Centroid
1542 FORMULA: C11H15NO3 1543 FORMULA: C11H15NO3
1543 INCHIKEY: ISRUGXGCCGIOQO-UHFFFAOYSA-N 1544 INCHIKEY: ISRUGXGCCGIOQO-UHFFFAOYSA-N
1546 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1547 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1547 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1548 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1548 IONIZATION: ESI+ 1549 IONIZATION: ESI+
1549 LICENSE: CC BY-NC 1550 LICENSE: CC BY-NC
1550 COMMENT: 1551 COMMENT:
1551 COMPOUND_NAME: Propoxur
1552 RETENTION_TIME: 3.894733 1552 RETENTION_TIME: 3.894733
1553 PRECURSOR_MZ: 210.1129 1553 PRECURSOR_MZ: 210.1129
1554 ADDUCT: [M+H]+ 1554 ADDUCT: [M+H]+
1555 COLLISION_ENERGY: 1555 COLLISION_ENERGY:
1556 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1556 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1557 NUM PEAKS: 6 1557 NUM PEAKS: 6
1558 93.03366 11976.0 1558 93.03366 11976.0
1559 111.04436 1112660.0 1559 111.04436 1112660.0
1560 153.09126 254920.0 1560 153.09126 254920.0
1561 168.06589 785437.0 1561 168.06589 785437.0
1562 199.97662 26875.0 1562 199.97662 26875.0
1563 210.11256 38244.0 1563 210.11256 38244.0
1564 1564
1565 COMPOUND_NAME: Neburon
1565 SCANNUMBER: 4942 1566 SCANNUMBER: 4942
1566 IONMODE: Positive 1567 IONMODE: Positive
1567 SPECTRUMTYPE: Centroid 1568 SPECTRUMTYPE: Centroid
1568 FORMULA: C12H16N2OCl2 1569 FORMULA: C12H16N2OCl2
1569 INCHIKEY: CCGPUGMWYLICGL-UHFFFAOYSA-N 1570 INCHIKEY: CCGPUGMWYLICGL-UHFFFAOYSA-N
1572 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1573 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1573 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1574 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1574 IONIZATION: ESI+ 1575 IONIZATION: ESI+
1575 LICENSE: CC BY-NC 1576 LICENSE: CC BY-NC
1576 COMMENT: 1577 COMMENT:
1577 COMPOUND_NAME: Neburon
1578 RETENTION_TIME: 6.834164 1578 RETENTION_TIME: 6.834164
1579 PRECURSOR_MZ: 275.0721 1579 PRECURSOR_MZ: 275.0721
1580 ADDUCT: [M+H]+ 1580 ADDUCT: [M+H]+
1581 COLLISION_ENERGY: 1581 COLLISION_ENERGY:
1582 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1582 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1583 NUM PEAKS: 12 1583 NUM PEAKS: 12
1584 88.11217 614563.0 1584 88.11217 614563.0
1585 114.09161 31817.0 1585 114.09161 31817.0
1586 123.99487 30163.0 1586 123.99487 30163.0
1587 125.00258 66386.0 1587 125.00258 66386.0
1588 127.01831 315476.0 1588 127.01831 315476.0
1589 132.96072 198326.0 1589 132.96072 198326.0
1590 152.99777 149347.0 1590 152.99777 149347.0
1591 159.97182 1502459.0 1591 159.97182 1502459.0
1592 161.98734 127589.0 1592 161.98734 127589.0
1593 172.9666 45053.0 1593 172.9666 45053.0
1594 173.50816 20256.0 1594 173.50816 20256.0
1595 187.96652 106090.0 1595 187.96652 106090.0
1596 1596
1597 COMPOUND_NAME: Pirimicarb
1597 SCANNUMBER: 1410 1598 SCANNUMBER: 1410
1598 IONMODE: Positive 1599 IONMODE: Positive
1599 SPECTRUMTYPE: Centroid 1600 SPECTRUMTYPE: Centroid
1600 FORMULA: C11H18N4O2 1601 FORMULA: C11H18N4O2
1601 INCHIKEY: YFGYUFNIOHWBOB-UHFFFAOYSA-N 1602 INCHIKEY: YFGYUFNIOHWBOB-UHFFFAOYSA-N
1604 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1605 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1605 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1606 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1606 IONIZATION: ESI+ 1607 IONIZATION: ESI+
1607 LICENSE: CC BY-NC 1608 LICENSE: CC BY-NC
1608 COMMENT: 1609 COMMENT:
1609 COMPOUND_NAME: Pirimicarb
1610 RETENTION_TIME: 2.886323 1610 RETENTION_TIME: 2.886323
1611 PRECURSOR_MZ: 239.1508 1611 PRECURSOR_MZ: 239.1508
1612 ADDUCT: [M+H]+ 1612 ADDUCT: [M+H]+
1613 COLLISION_ENERGY: 1613 COLLISION_ENERGY:
1614 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1614 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1615 NUM PEAKS: 16 1615 NUM PEAKS: 16
1616 85.07622 1062158.0 1616 85.07622 1062158.0
1617 94.05271 17085.0 1617 94.05271 17085.0
1618 109.07641 1234692.0 1618 109.07641 1234692.0
1619 123.0557 18419.0 1619 123.0557 18419.0
1620 124.06345 155955.0 1620 124.06345 155955.0
1621 137.07117 726268.0 1621 137.07117 726268.0
1622 138.0789 659866.0 1622 138.0789 659866.0
1623 139.08681 37108.0 1623 139.08681 37108.0
1624 150.10287 446134.0 1624 150.10287 446134.0
1625 152.08211 433568.0 1625 152.08211 433568.0
1626 166.09756 38582.0 1626 166.09756 38582.0
1627 167.10577 250650.0 1627 167.10577 250650.0
1628 168.11327 14402.0 1628 168.11327 14402.0
1629 180.11363 53047.0 1629 180.11363 53047.0
1630 182.12914 1046026.0 1630 182.12914 1046026.0
1631 195.16029 68565.0 1631 195.16029 68565.0
1632 1632
1633 COMPOUND_NAME: Promecarb
1633 SCANNUMBER: 3089 1634 SCANNUMBER: 3089
1634 IONMODE: Positive 1635 IONMODE: Positive
1635 SPECTRUMTYPE: Centroid 1636 SPECTRUMTYPE: Centroid
1636 FORMULA: C12H17NO2 1637 FORMULA: C12H17NO2
1637 INCHIKEY: DTAPQAJKAFRNJB-UHFFFAOYSA-N 1638 INCHIKEY: DTAPQAJKAFRNJB-UHFFFAOYSA-N
1640 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1641 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1641 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1642 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1642 IONIZATION: ESI+ 1643 IONIZATION: ESI+
1643 LICENSE: CC BY-NC 1644 LICENSE: CC BY-NC
1644 COMMENT: 1645 COMMENT:
1645 COMPOUND_NAME: Promecarb
1646 RETENTION_TIME: 5.65392 1646 RETENTION_TIME: 5.65392
1647 PRECURSOR_MZ: 208.1339 1647 PRECURSOR_MZ: 208.1339
1648 ADDUCT: [M+H]+ 1648 ADDUCT: [M+H]+
1649 COLLISION_ENERGY: 1649 COLLISION_ENERGY:
1650 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1650 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1651 NUM PEAKS: 3 1651 NUM PEAKS: 3
1652 109.0651 1911986.0 1652 109.0651 1911986.0
1653 151.1118 3833728.0 1653 151.1118 3833728.0
1654 208.13309 173991.0 1654 208.13309 173991.0
1655 1655
1656 COMPOUND_NAME: Ametryn
1656 SCANNUMBER: 2984 1657 SCANNUMBER: 2984
1657 IONMODE: Positive 1658 IONMODE: Positive
1658 SPECTRUMTYPE: Centroid 1659 SPECTRUMTYPE: Centroid
1659 FORMULA: C9H17N5S 1660 FORMULA: C9H17N5S
1660 INCHIKEY: RQVYBGPQFYCBGX-UHFFFAOYSA-N 1661 INCHIKEY: RQVYBGPQFYCBGX-UHFFFAOYSA-N
1663 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1664 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1664 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1665 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1665 IONIZATION: ESI+ 1666 IONIZATION: ESI+
1666 LICENSE: CC BY-NC 1667 LICENSE: CC BY-NC
1667 COMMENT: 1668 COMMENT:
1668 COMPOUND_NAME: Ametryn
1669 RETENTION_TIME: 4.38309 1669 RETENTION_TIME: 4.38309
1670 PRECURSOR_MZ: 228.1282 1670 PRECURSOR_MZ: 228.1282
1671 ADDUCT: [M+H]+ 1671 ADDUCT: [M+H]+
1672 COLLISION_ENERGY: 1672 COLLISION_ENERGY:
1673 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1673 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1674 NUM PEAKS: 15 1674 NUM PEAKS: 15
1675 85.05116 494786.0 1675 85.05116 494786.0
1676 91.03273 2410460.0 1676 91.03273 2410460.0
1677 96.05421 57071.0 1677 96.05421 57071.0
1678 96.05572 4102907.0 1678 96.05572 4102907.0
1679 102.03746 125646.0 1679 102.03746 125646.0
1680 110.04619 527391.0 1680 110.04619 527391.0
1681 113.08218 433234.0 1681 113.08218 433234.0
1682 116.0279 3479269.0 1682 116.0279 3479269.0
1683 138.07761 1659836.0 1683 138.07761 1659836.0
1684 140.09331 43027.0 1684 140.09331 43027.0
1685 144.05919 1428619.0 1685 144.05919 1428619.0
1686 158.04967 1355067.0 1686 158.04967 1355067.0
1687 184.06534 61690.0 1687 184.06534 61690.0
1688 186.08095 4152044.0 1688 186.08095 4152044.0
1689 228.12772 94575.0 1689 228.12772 94575.0
1690 1690
1691 COMPOUND_NAME: Azoxystrobin
1691 SCANNUMBER: 7002 1692 SCANNUMBER: 7002
1692 IONMODE: Positive 1693 IONMODE: Positive
1693 SPECTRUMTYPE: Centroid 1694 SPECTRUMTYPE: Centroid
1694 FORMULA: C22H17N3O5 1695 FORMULA: C22H17N3O5
1695 INCHIKEY: WFDXOXNFNRHQEC-UHFFFAOYSA-N 1696 INCHIKEY: WFDXOXNFNRHQEC-UHFFFAOYSA-N
1698 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1699 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1699 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1700 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1700 IONIZATION: ESI+ 1701 IONIZATION: ESI+
1701 LICENSE: CC BY-NC 1702 LICENSE: CC BY-NC
1702 COMMENT: 1703 COMMENT:
1703 COMPOUND_NAME: Azoxystrobin
1704 RETENTION_TIME: 6.9269 1704 RETENTION_TIME: 6.9269
1705 PRECURSOR_MZ: 404.1249 1705 PRECURSOR_MZ: 404.1249
1706 ADDUCT: [M+H]+ 1706 ADDUCT: [M+H]+
1707 COLLISION_ENERGY: 1707 COLLISION_ENERGY:
1708 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1708 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1709 NUM PEAKS: 46 1709 NUM PEAKS: 46
1710 120.04499 298934.0 1710 120.04499 298934.0
1711 129.04543 475852.0 1711 129.04543 475852.0
1712 130.0406 263606.0 1712 130.0406 263606.0
1713 133.05293 386291.0 1713 133.05293 386291.0
1714 134.06076 1413032.0 1714 134.06076 1413032.0
1715 141.04556 164042.0 1715 141.04556 164042.0
1716 143.06114 793237.0 1716 143.06114 793237.0
1717 145.02927 438571.0 1717 145.02927 438571.0
1718 145.0527 469026.0 1718 145.0527 469026.0
1719 155.06116 174099.0 1719 155.06116 174099.0
1720 156.04523 1265874.0 1720 156.04523 1265874.0
1721 169.04019 657911.0 1721 169.04019 657911.0
1722 170.04799 171763.0 1722 170.04799 171763.0
1723 171.03239 360415.0 1723 171.03239 360415.0
1724 171.05582 571918.0 1724 171.05582 571918.0
1725 172.03992 1796369.0 1725 172.03992 1796369.0
1726 173.04782 282353.0 1726 173.04782 282353.0
1727 177.05542 349400.0 1727 177.05542 349400.0
1728 182.04868 292236.0 1728 182.04868 292236.0
1729 182.0724 305597.0 1729 182.0724 305597.0
1730 183.05617 4029271.0 1730 183.05617 4029271.0
1731 199.05089 723420.0 1731 199.05089 723420.0
1732 200.03506 1025293.0 1732 200.03506 1025293.0
1733 201.04263 1807636.0 1733 201.04263 1807636.0
1734 201.06636 510108.0 1734 201.06636 510108.0
1735 210.04311 1974682.0 1735 210.04311 1974682.0
1736 210.0668 342264.0 1736 210.0668 342264.0
1737 211.05078 355209.0 1737 211.05078 355209.0
1738 216.06657 1168439.0 1738 216.06657 1168439.0
1739 246.07988 182890.0 1739 246.07988 182890.0
1740 272.0834 1282380.0 1740 272.0834 1282380.0
1741 273.06769 795436.0 1741 273.06769 795436.0
1742 273.0907 1168355.0 1742 273.0907 1168355.0
1743 274.07443 221912.0 1743 274.07443 221912.0
1744 275.08304 260482.0 1744 275.08304 260482.0
1745 287.08322 453884.0 1745 287.08322 453884.0
1746 288.06744 172169.0 1746 288.06744 172169.0
1747 300.07855 1244681.0 1747 300.07855 1244681.0
1748 301.08551 3241347.0 1748 301.08551 3241347.0
1749 312.07855 219216.0 1749 312.07855 219216.0
1750 315.10245 205186.0 1750 315.10245 205186.0
1751 316.10916 292099.0 1751 316.10916 292099.0
1752 328.07382 3766201.0 1752 328.07382 3766201.0
1753 329.08087 15964814.0 1753 329.08087 15964814.0
1754 344.10461 2718360.0 1754 344.10461 2718360.0
1755 372.10004 167044.0 1755 372.10004 167044.0
1756 1756
1757 COMPOUND_NAME: Benalaxyl
1757 SCANNUMBER: 7850 1758 SCANNUMBER: 7850
1758 IONMODE: Positive 1759 IONMODE: Positive
1759 SPECTRUMTYPE: Centroid 1760 SPECTRUMTYPE: Centroid
1760 FORMULA: C20H23NO3 1761 FORMULA: C20H23NO3
1761 INCHIKEY: CJPQIRJHIZUAQP-INIZCTEOSA-N 1762 INCHIKEY: CJPQIRJHIZUAQP-INIZCTEOSA-N
1764 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1765 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1765 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1766 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1766 IONIZATION: ESI+ 1767 IONIZATION: ESI+
1767 LICENSE: CC BY-NC 1768 LICENSE: CC BY-NC
1768 COMMENT: 1769 COMMENT:
1769 COMPOUND_NAME: Benalaxyl
1770 RETENTION_TIME: 7.079875 1770 RETENTION_TIME: 7.079875
1771 PRECURSOR_MZ: 326.1756 1771 PRECURSOR_MZ: 326.1756
1772 ADDUCT: [M+H]+ 1772 ADDUCT: [M+H]+
1773 COLLISION_ENERGY: 1773 COLLISION_ENERGY:
1774 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1774 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1775 NUM PEAKS: 8 1775 NUM PEAKS: 8
1776 91.05441 11560916.0 1776 91.05441 11560916.0
1777 105.0702 367839.0 1777 105.0702 367839.0
1778 106.06546 647312.0 1778 106.06546 647312.0
1779 120.081 385637.0 1779 120.081 385637.0
1780 121.08883 11501126.0 1780 121.08883 11501126.0
1781 122.09673 517871.0 1781 122.09673 517871.0
1782 133.08878 546024.0 1782 133.08878 546024.0
1783 148.11217 23207426.0 1783 148.11217 23207426.0
1784 1784
1785 COMPOUND_NAME: Boscalid
1785 SCANNUMBER: 6328 1786 SCANNUMBER: 6328
1786 IONMODE: Positive 1787 IONMODE: Positive
1787 SPECTRUMTYPE: Centroid 1788 SPECTRUMTYPE: Centroid
1788 FORMULA: C18H12N2OCl2 1789 FORMULA: C18H12N2OCl2
1789 INCHIKEY: WYEMLYFITZORAB-UHFFFAOYSA-N 1790 INCHIKEY: WYEMLYFITZORAB-UHFFFAOYSA-N
1792 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1793 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1793 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1794 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1794 IONIZATION: ESI+ 1795 IONIZATION: ESI+
1795 LICENSE: CC BY-NC 1796 LICENSE: CC BY-NC
1796 COMMENT: 1797 COMMENT:
1797 COMPOUND_NAME: Boscalid
1798 RETENTION_TIME: 6.811709 1798 RETENTION_TIME: 6.811709
1799 PRECURSOR_MZ: 343.0408 1799 PRECURSOR_MZ: 343.0408
1800 ADDUCT: [M+H]+ 1800 ADDUCT: [M+H]+
1801 COLLISION_ENERGY: 1801 COLLISION_ENERGY:
1802 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1802 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1803 NUM PEAKS: 27 1803 NUM PEAKS: 27
1804 96.04461 588528.0 1804 96.04461 588528.0
1805 111.99506 131288.0 1805 111.99506 131288.0
1806 112.03961 562594.0 1806 112.03961 562594.0
1807 114.01087 183518.0 1807 114.01087 183518.0
1808 130.00558 256565.0 1808 130.00558 256565.0
1809 139.99011 1220289.0 1809 139.99011 1220289.0
1810 152.06248 66998.0 1810 152.06248 66998.0
1811 216.08105 60699.0 1811 216.08105 60699.0
1812 227.07349 93814.0 1812 227.07349 93814.0
1813 228.08148 96430.0 1813 228.08148 96430.0
1814 229.08876 93365.0 1814 229.08876 93365.0
1815 230.03716 77307.0 1815 230.03716 77307.0
1816 238.04195 58994.0 1816 238.04195 58994.0
1817 242.08464 181011.0 1817 242.08464 181011.0
1818 243.09259 680474.0 1818 243.09259 680474.0
1819 244.09969 317520.0 1819 244.09969 317520.0
1820 253.07672 424600.0 1820 253.07672 424600.0
1821 254.08458 657164.0 1821 254.08458 657164.0
1822 264.05807 118437.0 1822 264.05807 118437.0
1823 270.07944 187992.0 1823 270.07944 187992.0
1824 271.08762 5868577.0 1824 271.08762 5868577.0
1825 272.09424 5476461.0 1825 272.09424 5476461.0
1826 279.0686 68522.0 1826 279.0686 68522.0
1827 289.05276 1245064.0 1827 289.05276 1245064.0
1828 305.04871 107573.0 1828 305.04871 107573.0
1829 306.05643 72921.0 1829 306.05643 72921.0
1830 307.06335 2958245.0 1830 307.06335 2958245.0
1831 1831
1832 COMPOUND_NAME: Carbetamide
1832 SCANNUMBER: 2756 1833 SCANNUMBER: 2756
1833 IONMODE: Positive 1834 IONMODE: Positive
1834 SPECTRUMTYPE: Centroid 1835 SPECTRUMTYPE: Centroid
1835 FORMULA: C12H16N2O3 1836 FORMULA: C12H16N2O3
1836 INCHIKEY: AMRQXHFXNZFDCH-VIFPVBQESA-N 1837 INCHIKEY: AMRQXHFXNZFDCH-VIFPVBQESA-N
1839 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1840 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1840 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1841 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1841 IONIZATION: ESI+ 1842 IONIZATION: ESI+
1842 LICENSE: CC BY-NC 1843 LICENSE: CC BY-NC
1843 COMMENT: 1844 COMMENT:
1844 COMPOUND_NAME: Carbetamide
1845 RETENTION_TIME: 3.923062 1845 RETENTION_TIME: 3.923062
1846 PRECURSOR_MZ: 237.1238 1846 PRECURSOR_MZ: 237.1238
1847 ADDUCT: [M+H]+ 1847 ADDUCT: [M+H]+
1848 COLLISION_ENERGY: 1848 COLLISION_ENERGY:
1849 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1849 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1850 NUM PEAKS: 12 1850 NUM PEAKS: 12
1851 85.07622 86855.0 1851 85.07622 86855.0
1852 100.07591 86451.0 1852 100.07591 86451.0
1853 118.08654 1614784.0 1853 118.08654 1614784.0
1854 120.04464 757563.0 1854 120.04464 757563.0
1855 126.01047 99599.0 1855 126.01047 99599.0
1856 138.05496 54640.0 1856 138.05496 54640.0
1857 144.06567 88684.0 1857 144.06567 88684.0
1858 164.0705 45687.0 1858 164.0705 45687.0
1859 192.0659 2143350.0 1859 192.0659 2143350.0
1860 237.07993 102575.0 1860 237.07993 102575.0
1861 237.09068 314588.0 1861 237.09068 314588.0
1862 237.12401 187935.0 1862 237.12401 187935.0
1863 1863
1864 COMPOUND_NAME: Carfentrazone ethyl
1864 SCANNUMBER: 6914 1865 SCANNUMBER: 6914
1865 IONMODE: Positive 1866 IONMODE: Positive
1866 SPECTRUMTYPE: Centroid 1867 SPECTRUMTYPE: Centroid
1867 FORMULA: C15H14N3O3Cl2F3 1868 FORMULA: C15H14N3O3Cl2F3
1868 INCHIKEY: MLKCGVHIFJBRCD-JTQLQIEISA-N 1869 INCHIKEY: MLKCGVHIFJBRCD-JTQLQIEISA-N
1871 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1872 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1872 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1873 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1873 IONIZATION: ESI+ 1874 IONIZATION: ESI+
1874 LICENSE: CC BY-NC 1875 LICENSE: CC BY-NC
1875 COMMENT: 1876 COMMENT:
1876 COMPOUND_NAME: Carfentrazone ethyl
1877 RETENTION_TIME: 6.898515 1877 RETENTION_TIME: 6.898515
1878 PRECURSOR_MZ: 412.045 1878 PRECURSOR_MZ: 412.045
1879 ADDUCT: [M+H]+ 1879 ADDUCT: [M+H]+
1880 COLLISION_ENERGY: 1880 COLLISION_ENERGY:
1881 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1881 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1882 NUM PEAKS: 75 1882 NUM PEAKS: 75
1883 87.03558 102938.0 1883 87.03558 102938.0
1884 92.03108 108928.0 1884 92.03108 108928.0
1885 140.99028 93612.0 1885 140.99028 93612.0
1886 168.00159 290200.0 1886 168.00159 290200.0
1887 168.98535 256214.0 1887 168.98535 256214.0
1888 169.00954 280404.0 1888 169.00954 280404.0
1889 169.99326 139258.0 1889 169.99326 139258.0
1890 176.0387 59605.0 1890 176.0387 59605.0
1891 176.96758 2472383.0 1891 176.96758 2472383.0
1892 183.0123 267100.0 1892 183.0123 267100.0
1893 183.99632 81664.0 1893 183.99632 81664.0
1894 186.01216 91455.0 1894 186.01216 91455.0
1895 194.98845 136592.0 1895 194.98845 136592.0
1896 195.99637 326492.0 1896 195.99637 326492.0
1897 197.00471 52605.0 1897 197.00471 52605.0
1898 201.9623 154634.0 1898 201.9623 154634.0
1899 203.97847 447264.0 1899 203.97847 447264.0
1900 204.96245 1832179.0 1900 204.96245 1832179.0
1901 206.02895 92544.0 1901 206.02895 92544.0
1902 207.03662 171674.0 1902 207.03662 171674.0
1903 209.02803 384802.0 1903 209.02803 384802.0
1904 209.99982 113563.0 1904 209.99982 113563.0
1905 211.00719 472507.0 1905 211.00719 472507.0
1906 212.01517 66934.0 1906 212.01517 66934.0
1907 213.00288 312895.0 1907 213.00288 312895.0
1908 214.01096 51013.0 1908 214.01096 51013.0
1909 215.02534 55407.0 1909 215.02534 55407.0
1910 220.9915 95557.0 1910 220.9915 95557.0
1911 221.97609 58129.0 1911 221.97609 58129.0
1912 222.00006 181469.0 1912 222.00006 181469.0
1913 223.00748 74723.0 1913 223.00748 74723.0
1914 223.9912 1241221.0 1914 223.9912 1241221.0
1915 226.03568 99992.0 1915 226.03568 99992.0
1916 227.98999 56867.0 1916 227.98999 56867.0
1917 228.9734 154659.0 1917 228.9734 154659.0
1918 228.99759 849754.0 1918 228.99759 849754.0
1919 229.9576 291454.0 1919 229.9576 291454.0
1920 230.96507 364210.0 1920 230.96507 364210.0
1921 231.97353 309882.0 1921 231.97353 309882.0
1922 232.98094 634253.0 1922 232.98094 634253.0
1923 233.00957 190835.0 1923 233.00957 190835.0
1924 233.99303 64478.0 1924 233.99303 64478.0
1925 236.01566 50291.0 1925 236.01566 50291.0
1926 239.00291 79639.0 1926 239.00291 79639.0
1927 240.99757 4112806.0 1927 240.99757 4112806.0
1928 242.00581 1279056.0 1928 242.00581 1279056.0
1929 246.98367 100821.0 1929 246.98367 100821.0
1930 248.98016 83634.0 1930 248.98016 83634.0
1931 248.9865 48588.0 1931 248.9865 48588.0
1932 249.9944 112801.0 1932 249.9944 112801.0
1933 251.02658 84213.0 1933 251.02658 84213.0
1934 252.03403 720952.0 1934 252.03403 720952.0
1935 256.96869 464576.0 1935 256.96869 464576.0
1936 257.95212 120792.0 1936 257.95212 120792.0
1937 258.96021 600062.0 1937 258.96021 600062.0
1938 261.00433 486923.0 1938 261.00433 486923.0
1939 268.00449 56951.0 1939 268.00449 56951.0
1940 268.99277 70677.0 1940 268.99277 70677.0
1941 270.00082 107703.0 1941 270.00082 107703.0
1942 270.98462 439596.0 1942 270.98462 439596.0
1943 274.97897 367619.0 1943 274.97897 367619.0
1944 276.97476 4577284.0 1944 276.97476 4577284.0
1945 280.02945 127558.0 1945 280.02945 127558.0
1946 282.0246 396042.0 1946 282.0246 396042.0
1947 284.96323 117220.0 1947 284.96323 117220.0
1948 288.01102 1894072.0 1948 288.01102 1894072.0
1949 290.03122 319337.0 1949 290.03122 319337.0
1950 298.97946 85527.0 1950 298.97946 85527.0
1951 302.03137 2921622.0 1951 302.03137 2921622.0
1952 303.0383 181158.0 1952 303.0383 181158.0
1953 316.00662 372285.0 1953 316.00662 372285.0
1954 318.00153 484008.0 1954 318.00153 484008.0
1955 320.04153 58056.0 1955 320.04153 58056.0
1956 338.00775 410316.0 1956 338.00775 410316.0
1957 345.99677 2618042.0 1957 345.99677 2618042.0
1958 1958
1959 COMPOUND_NAME: Chlorantraniliprole
1959 SCANNUMBER: 5260 1960 SCANNUMBER: 5260
1960 IONMODE: Positive 1961 IONMODE: Positive
1961 SPECTRUMTYPE: Centroid 1962 SPECTRUMTYPE: Centroid
1962 FORMULA: C18H14N5O2BrCl2 1963 FORMULA: C18H14N5O2BrCl2
1963 INCHIKEY: PSOVNZZNOMJUBI-UHFFFAOYSA-N 1964 INCHIKEY: PSOVNZZNOMJUBI-UHFFFAOYSA-N
1966 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1967 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1967 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1968 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1968 IONIZATION: ESI+ 1969 IONIZATION: ESI+
1969 LICENSE: CC BY-NC 1970 LICENSE: CC BY-NC
1970 COMMENT: 1971 COMMENT:
1971 COMPOUND_NAME: Chlorantraniliprole
1972 RETENTION_TIME: 6.589343 1972 RETENTION_TIME: 6.589343
1973 PRECURSOR_MZ: 481.9785 1973 PRECURSOR_MZ: 481.9785
1974 ADDUCT: [M+H]+ 1974 ADDUCT: [M+H]+
1975 COLLISION_ENERGY: 1975 COLLISION_ENERGY:
1976 INSTRUMENT_TYPE: LC-ESI-Orbitrap 1976 INSTRUMENT_TYPE: LC-ESI-Orbitrap
1977 NUM PEAKS: 4 1977 NUM PEAKS: 4
1978 283.92297 5735542.0 1978 283.92297 5735542.0
1979 450.93774 4907420.0 1979 450.93774 4907420.0
1980 463.96796 71876.0 1980 463.96796 71876.0
1981 481.97949 1501231.0 1981 481.97949 1501231.0
1982 1982
1983 COMPOUND_NAME: Clofentezine
1983 SCANNUMBER: 9818 1984 SCANNUMBER: 9818
1984 IONMODE: Positive 1985 IONMODE: Positive
1985 SPECTRUMTYPE: Centroid 1986 SPECTRUMTYPE: Centroid
1986 FORMULA: C14H8N4Cl2 1987 FORMULA: C14H8N4Cl2
1987 INCHIKEY: UXADOQPNKNTIHB-UHFFFAOYSA-N 1988 INCHIKEY: UXADOQPNKNTIHB-UHFFFAOYSA-N
1990 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 1991 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
1991 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 1992 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
1992 IONIZATION: ESI+ 1993 IONIZATION: ESI+
1993 LICENSE: CC BY-NC 1994 LICENSE: CC BY-NC
1994 COMMENT: 1995 COMMENT:
1995 COMPOUND_NAME: Clofentezine
1996 RETENTION_TIME: 7.397017 1996 RETENTION_TIME: 7.397017
1997 PRECURSOR_MZ: 303.0207 1997 PRECURSOR_MZ: 303.0207
1998 ADDUCT: [M+H]+ 1998 ADDUCT: [M+H]+
1999 COLLISION_ENERGY: 1999 COLLISION_ENERGY:
2000 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2000 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2001 NUM PEAKS: 5 2001 NUM PEAKS: 5
2002 92.0498 44376.0 2002 92.0498 44376.0
2003 102.03414 382179.0 2003 102.03414 382179.0
2004 120.04463 495630.0 2004 120.04463 495630.0
2005 130.04021 2783936.0 2005 130.04021 2783936.0
2006 138.01057 2494447.0 2006 138.01057 2494447.0
2007 2007
2008 COMPOUND_NAME: Cyprodinil
2008 SCANNUMBER: 5584 2009 SCANNUMBER: 5584
2009 IONMODE: Positive 2010 IONMODE: Positive
2010 SPECTRUMTYPE: Centroid 2011 SPECTRUMTYPE: Centroid
2011 FORMULA: C14H15N3 2012 FORMULA: C14H15N3
2012 INCHIKEY: HAORKNGNJCEJBX-UHFFFAOYSA-N 2013 INCHIKEY: HAORKNGNJCEJBX-UHFFFAOYSA-N
2015 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2016 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2016 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2017 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2017 IONIZATION: ESI+ 2018 IONIZATION: ESI+
2018 LICENSE: CC BY-NC 2019 LICENSE: CC BY-NC
2019 COMMENT: 2020 COMMENT:
2020 COMPOUND_NAME: Cyprodinil
2021 RETENTION_TIME: 6.669806 2021 RETENTION_TIME: 6.669806
2022 PRECURSOR_MZ: 226.1346 2022 PRECURSOR_MZ: 226.1346
2023 ADDUCT: [M+H]+ 2023 ADDUCT: [M+H]+
2024 COLLISION_ENERGY: 2024 COLLISION_ENERGY:
2025 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2025 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2026 NUM PEAKS: 68 2026 NUM PEAKS: 68
2027 89.03882 250501.0 2027 89.03882 250501.0
2028 91.05441 2917894.0 2028 91.05441 2917894.0
2029 92.0498 1832571.0 2029 92.0498 1832571.0
2030 92.06236 327913.0 2030 92.06236 327913.0
2031 93.0575 7935048.0 2031 93.0575 7935048.0
2032 94.06544 551055.0 2032 94.06544 551055.0
2033 95.04928 1106686.0 2033 95.04928 1106686.0
2034 104.04984 578815.0 2034 104.04984 578815.0
2035 105.04505 751939.0 2035 105.04505 751939.0
2036 106.06546 3348979.0 2036 106.06546 3348979.0
2037 107.07314 366893.0 2037 107.07314 366893.0
2038 108.06842 996581.0 2038 108.06842 996581.0
2039 108.08108 5293585.0 2039 108.08108 5293585.0
2040 109.0761 435067.0 2040 109.0761 435067.0
2041 110.06014 373109.0 2041 110.06014 373109.0
2042 115.0543 340655.0 2042 115.0543 340655.0
2043 116.0497 1136768.0 2043 116.0497 1136768.0
2044 117.0574 936588.0 2044 117.0574 936588.0
2045 118.05279 3491518.0 2045 118.05279 3491518.0
2046 118.06519 1243941.0 2046 118.06519 1243941.0
2047 119.06059 3591314.0 2047 119.06059 3591314.0
2048 123.09197 364628.0 2048 123.09197 364628.0
2049 124.07606 563904.0 2049 124.07606 563904.0
2050 130.06528 192669.0 2050 130.06528 192669.0
2051 131.06062 1377516.0 2051 131.06062 1377516.0
2052 132.06825 1932161.0 2052 132.06825 1932161.0
2053 133.07642 3211678.0 2053 133.07642 3211678.0
2054 134.06033 753709.0 2054 134.06033 753709.0
2055 142.06525 584454.0 2055 142.06525 584454.0
2056 143.06068 1778669.0 2056 143.06068 1778669.0
2057 143.07307 279220.0 2057 143.07307 279220.0
2058 144.05594 191195.0 2058 144.05594 191195.0
2059 144.08099 2104332.0 2059 144.08099 2104332.0
2060 145.07616 882365.0 2060 145.07616 882365.0
2061 149.07127 251299.0 2061 149.07127 251299.0
2062 156.06825 169085.0 2062 156.06825 169085.0
2063 157.0762 329957.0 2063 157.0762 329957.0
2064 158.0838 181590.0 2064 158.0838 181590.0
2065 159.09198 963940.0 2065 159.09198 963940.0
2066 165.06998 303199.0 2066 165.06998 303199.0
2067 167.06058 287846.0 2067 167.06058 287846.0
2068 167.07332 1087973.0 2068 167.07332 1087973.0
2069 168.06824 523675.0 2069 168.06824 523675.0
2070 168.08109 896186.0 2070 168.08109 896186.0
2071 169.07619 575896.0 2071 169.07619 575896.0
2072 170.0843 204211.0 2072 170.0843 204211.0
2073 171.09184 238779.0 2073 171.09184 238779.0
2074 181.07629 410526.0 2074 181.07629 410526.0
2075 182.08427 540213.0 2075 182.08427 540213.0
2076 182.09682 243307.0 2076 182.09682 243307.0
2077 183.07944 619682.0 2077 183.07944 619682.0
2078 183.09206 583441.0 2078 183.09206 583441.0
2079 184.08746 1461784.0 2079 184.08746 1461784.0
2080 185.10789 904319.0 2080 185.10789 904319.0
2081 191.07323 180652.0 2081 191.07323 180652.0
2082 193.07642 1237200.0 2082 193.07642 1237200.0
2083 194.08405 2240403.0 2083 194.08405 2240403.0
2084 196.08698 270421.0 2084 196.08698 270421.0
2085 197.09528 430359.0 2085 197.09528 430359.0
2086 198.10313 664506.0 2086 198.10313 664506.0
2087 199.11044 212040.0 2087 199.11044 212040.0
2088 207.0918 1191559.0 2088 207.0918 1191559.0
2089 208.10004 666594.0 2089 208.10004 666594.0
2090 209.10754 1644491.0 2090 209.10754 1644491.0
2091 210.10275 4134248.0 2091 210.10275 4134248.0
2092 211.11086 699261.0 2092 211.11086 699261.0
2093 224.1181 912227.0 2093 224.1181 912227.0
2094 226.13422 16374867.0 2094 226.13422 16374867.0
2095 2095
2096 COMPOUND_NAME: Cyromazine_1
2096 SCANNUMBER: 614 2097 SCANNUMBER: 614
2097 IONMODE: Positive 2098 IONMODE: Positive
2098 SPECTRUMTYPE: Centroid 2099 SPECTRUMTYPE: Centroid
2099 FORMULA: C6H10N6 2100 FORMULA: C6H10N6
2100 INCHIKEY: LVQDKIWDGQRHTE-UHFFFAOYSA-N 2101 INCHIKEY: LVQDKIWDGQRHTE-UHFFFAOYSA-N
2103 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2104 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2104 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2105 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2105 IONIZATION: ESI+ 2106 IONIZATION: ESI+
2106 LICENSE: CC BY-NC 2107 LICENSE: CC BY-NC
2107 COMMENT: 2108 COMMENT:
2108 COMPOUND_NAME: Cyromazine_1
2109 RETENTION_TIME: 0.7250975 2109 RETENTION_TIME: 0.7250975
2110 PRECURSOR_MZ: 167.1043 2110 PRECURSOR_MZ: 167.1043
2111 ADDUCT: [M+H]+ 2111 ADDUCT: [M+H]+
2112 COLLISION_ENERGY: 2112 COLLISION_ENERGY:
2113 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2113 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2114 NUM PEAKS: 9 2114 NUM PEAKS: 9
2115 85.05116 569181.0 2115 85.05116 569181.0
2116 108.05576 364390.0 2116 108.05576 364390.0
2117 110.0462 49797.0 2117 110.0462 49797.0
2118 125.08251 178192.0 2118 125.08251 178192.0
2119 127.07288 24861.0 2119 127.07288 24861.0
2120 139.07271 33973.0 2120 139.07271 33973.0
2121 150.0777 7345.0 2121 150.0777 7345.0
2122 151.07292 35146.0 2122 151.07292 35146.0
2123 167.10403 54669.0 2123 167.10403 54669.0
2124 2124
2125 COMPOUND_NAME: Cyromazine_2
2125 SCANNUMBER: 946 2126 SCANNUMBER: 946
2126 IONMODE: Positive 2127 IONMODE: Positive
2127 SPECTRUMTYPE: Centroid 2128 SPECTRUMTYPE: Centroid
2128 FORMULA: C6H10N6 2129 FORMULA: C6H10N6
2129 INCHIKEY: LVQDKIWDGQRHTE-UHFFFAOYSA-N 2130 INCHIKEY: LVQDKIWDGQRHTE-UHFFFAOYSA-N
2132 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2133 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2133 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2134 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2134 IONIZATION: ESI+ 2135 IONIZATION: ESI+
2135 LICENSE: CC BY-NC 2136 LICENSE: CC BY-NC
2136 COMMENT: 2137 COMMENT:
2137 COMPOUND_NAME: Cyromazine_2
2138 RETENTION_TIME: 1.057777 2138 RETENTION_TIME: 1.057777
2139 PRECURSOR_MZ: 167.1043 2139 PRECURSOR_MZ: 167.1043
2140 ADDUCT: [M+H]+ 2140 ADDUCT: [M+H]+
2141 COLLISION_ENERGY: 2141 COLLISION_ENERGY:
2142 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2142 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2143 NUM PEAKS: 12 2143 NUM PEAKS: 12
2144 85.05095 323769.0 2144 85.05095 323769.0
2145 100.08693 5287.0 2145 100.08693 5287.0
2146 108.05576 223896.0 2146 108.05576 223896.0
2147 110.0462 30873.0 2147 110.0462 30873.0
2148 112.06189 4105.0 2148 112.06189 4105.0
2149 125.08213 95867.0 2149 125.08213 95867.0
2150 127.07288 11228.0 2150 127.07288 11228.0
2151 139.07271 22781.0 2151 139.07271 22781.0
2152 150.0777 3986.0 2152 150.0777 3986.0
2153 151.07292 16833.0 2153 151.07292 16833.0
2154 155.01868 3272.0 2154 155.01868 3272.0
2155 167.10403 33800.0 2155 167.10403 33800.0
2156 2156
2157 COMPOUND_NAME: Dimoxystrobin
2157 SCANNUMBER: 7508 2158 SCANNUMBER: 7508
2158 IONMODE: Positive 2159 IONMODE: Positive
2159 SPECTRUMTYPE: Centroid 2160 SPECTRUMTYPE: Centroid
2160 FORMULA: C19H22N2O3 2161 FORMULA: C19H22N2O3
2161 INCHIKEY: WXUZAHCNPWONDH-UHFFFAOYSA-N 2162 INCHIKEY: WXUZAHCNPWONDH-UHFFFAOYSA-N
2164 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2165 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2165 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2166 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2166 IONIZATION: ESI+ 2167 IONIZATION: ESI+
2167 LICENSE: CC BY-NC 2168 LICENSE: CC BY-NC
2168 COMMENT: 2169 COMMENT:
2169 COMPOUND_NAME: Dimoxystrobin
2170 RETENTION_TIME: 7.042906 2170 RETENTION_TIME: 7.042906
2171 PRECURSOR_MZ: 327.1716 2171 PRECURSOR_MZ: 327.1716
2172 ADDUCT: [M+H]+ 2172 ADDUCT: [M+H]+
2173 COLLISION_ENERGY: 2173 COLLISION_ENERGY:
2174 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2174 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2175 NUM PEAKS: 25 2175 NUM PEAKS: 25
2176 89.03882 267042.0 2176 89.03882 267042.0
2177 91.05465 1177860.0 2177 91.05465 1177860.0
2178 92.05786 587003.0 2178 92.05786 587003.0
2179 106.06546 63219.0 2179 106.06546 63219.0
2180 116.0497 4287725.0 2180 116.0497 4287725.0
2181 117.0574 207058.0 2181 117.0574 207058.0
2182 118.06553 62777.0 2182 118.06553 62777.0
2183 121.06523 72575.0 2183 121.06523 72575.0
2184 121.08883 992075.0 2184 121.08883 992075.0
2185 122.09238 613096.0 2185 122.09238 613096.0
2186 134.06033 559976.0 2186 134.06033 559976.0
2187 135.08092 79495.0 2187 135.08092 79495.0
2188 148.07639 58182.0 2188 148.07639 58182.0
2189 148.11266 1671042.0 2189 148.11266 1671042.0
2190 149.10986 53924.0 2190 149.10986 53924.0
2191 149.11572 1649040.0 2191 149.11572 1649040.0
2192 178.0778 129475.0 2192 178.0778 129475.0
2193 180.08119 207313.0 2193 180.08119 207313.0
2194 193.10162 104706.0 2194 193.10162 104706.0
2195 194.09711 110382.0 2195 194.09711 110382.0
2196 195.10469 223024.0 2196 195.10469 223024.0
2197 221.09647 105352.0 2197 221.09647 105352.0
2198 222.09152 46935.0 2198 222.09152 46935.0
2199 222.10396 66419.0 2199 222.10396 66419.0
2200 223.09956 719508.0 2200 223.09956 719508.0
2201 2201
2202 COMPOUND_NAME: Fenazaquin
2202 SCANNUMBER: 11226 2203 SCANNUMBER: 11226
2203 IONMODE: Positive 2204 IONMODE: Positive
2204 SPECTRUMTYPE: Centroid 2205 SPECTRUMTYPE: Centroid
2205 FORMULA: C20H22N2O 2206 FORMULA: C20H22N2O
2206 INCHIKEY: DMYHGDXADUDKCQ-UHFFFAOYSA-N 2207 INCHIKEY: DMYHGDXADUDKCQ-UHFFFAOYSA-N
2209 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2210 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2210 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2211 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2211 IONIZATION: ESI+ 2212 IONIZATION: ESI+
2212 LICENSE: CC BY-NC 2213 LICENSE: CC BY-NC
2213 COMMENT: 2214 COMMENT:
2214 COMPOUND_NAME: Fenazaquin
2215 RETENTION_TIME: 7.977267 2215 RETENTION_TIME: 7.977267
2216 PRECURSOR_MZ: 307.1813 2216 PRECURSOR_MZ: 307.1813
2217 ADDUCT: [M+H]+ 2217 ADDUCT: [M+H]+
2218 COLLISION_ENERGY: 2218 COLLISION_ENERGY:
2219 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2219 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2220 NUM PEAKS: 14 2220 NUM PEAKS: 14
2221 91.05441 199112.0 2221 91.05441 199112.0
2222 103.05439 73599.0 2222 103.05439 73599.0
2223 104.04984 64148.0 2223 104.04984 64148.0
2224 105.0702 917430.0 2224 105.0702 917430.0
2225 117.06997 181158.0 2225 117.06997 181158.0
2226 119.0857 712865.0 2226 119.0857 712865.0
2227 121.10135 76811.0 2227 121.10135 76811.0
2228 130.02905 143777.0 2228 130.02905 143777.0
2229 131.08598 2116571.0 2229 131.08598 2116571.0
2230 133.10155 485868.0 2230 133.10155 485868.0
2231 145.10149 85536.0 2231 145.10149 85536.0
2232 146.10915 4833104.0 2232 146.10915 4833104.0
2233 147.05551 4215618.0 2233 147.05551 4215618.0
2234 161.13255 3701806.0 2234 161.13255 3701806.0
2235 2235
2236 COMPOUND_NAME: Fenhexamid
2236 SCANNUMBER: 5614 2237 SCANNUMBER: 5614
2237 IONMODE: Positive 2238 IONMODE: Positive
2238 SPECTRUMTYPE: Centroid 2239 SPECTRUMTYPE: Centroid
2239 FORMULA: C14H17NO2Cl2 2240 FORMULA: C14H17NO2Cl2
2240 INCHIKEY: VDLGAVXLJYLFDH-UHFFFAOYSA-N 2241 INCHIKEY: VDLGAVXLJYLFDH-UHFFFAOYSA-N
2243 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2244 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2244 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2245 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2245 IONIZATION: ESI+ 2246 IONIZATION: ESI+
2246 LICENSE: CC BY-NC 2247 LICENSE: CC BY-NC
2247 COMMENT: 2248 COMMENT:
2248 COMPOUND_NAME: Fenhexamid
2249 RETENTION_TIME: 6.679342 2249 RETENTION_TIME: 6.679342
2250 PRECURSOR_MZ: 302.0717 2250 PRECURSOR_MZ: 302.0717
2251 ADDUCT: [M+H]+ 2251 ADDUCT: [M+H]+
2252 COLLISION_ENERGY: 2252 COLLISION_ENERGY:
2253 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2253 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2254 NUM PEAKS: 6 2254 NUM PEAKS: 6
2255 95.01299 111399.0 2255 95.01299 111399.0
2256 97.10134 4001007.0 2256 97.10134 4001007.0
2257 142.00574 470488.0 2257 142.00574 470488.0
2258 143.0134 1124724.0 2258 143.0134 1124724.0
2259 177.98218 162637.0 2259 177.98218 162637.0
2260 302.0708 49250.0 2260 302.0708 49250.0
2261 2261
2262 COMPOUND_NAME: Fenpyroximate
2262 SCANNUMBER: 10879 2263 SCANNUMBER: 10879
2263 IONMODE: Positive 2264 IONMODE: Positive
2264 SPECTRUMTYPE: Centroid 2265 SPECTRUMTYPE: Centroid
2265 FORMULA: C24H27N3O4 2266 FORMULA: C24H27N3O4
2266 INCHIKEY: YYJNOYZRYGDPNH-UHFFFAOYSA-N 2267 INCHIKEY: YYJNOYZRYGDPNH-UHFFFAOYSA-N
2269 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2270 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2270 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2271 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2271 IONIZATION: ESI+ 2272 IONIZATION: ESI+
2272 LICENSE: CC BY-NC 2273 LICENSE: CC BY-NC
2273 COMMENT: 2274 COMMENT:
2274 COMPOUND_NAME: Fenpyroximate
2275 RETENTION_TIME: 7.825895 2275 RETENTION_TIME: 7.825895
2276 PRECURSOR_MZ: 422.2081 2276 PRECURSOR_MZ: 422.2081
2277 ADDUCT: [M+H]+ 2277 ADDUCT: [M+H]+
2278 COLLISION_ENERGY: 2278 COLLISION_ENERGY:
2279 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2279 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2280 NUM PEAKS: 90 2280 NUM PEAKS: 90
2281 91.04206 117996.0 2281 91.04206 117996.0
2282 91.05465 106024.0 2282 91.05465 106024.0
2283 92.0498 87696.0 2283 92.0498 87696.0
2284 93.05774 260654.0 2284 93.05774 260654.0
2285 94.04169 108699.0 2285 94.04169 108699.0
2286 95.04953 62385.0 2286 95.04953 62385.0
2287 95.06073 350683.0 2287 95.06073 350683.0
2288 96.06861 923552.0 2288 96.06861 923552.0
2289 104.04984 232471.0 2289 104.04984 232471.0
2290 106.06546 218843.0 2290 106.06546 218843.0
2291 107.02439 77423.0 2291 107.02439 77423.0
2292 107.04966 430579.0 2292 107.04966 430579.0
2293 109.04004 148437.0 2293 109.04004 148437.0
2294 110.0716 266167.0 2294 110.0716 266167.0
2295 111.05566 267693.0 2295 111.05566 267693.0
2296 112.06348 143921.0 2296 112.06348 143921.0
2297 113.07121 165810.0 2297 113.07121 165810.0
2298 117.05774 475621.0 2298 117.05774 475621.0
2299 118.06553 207059.0 2299 118.06553 207059.0
2300 121.0638 98676.0 2300 121.0638 98676.0
2301 121.07632 211577.0 2301 121.07632 211577.0
2302 122.07175 1015735.0 2302 122.07175 1015735.0
2303 123.05569 588803.0 2303 123.05569 588803.0
2304 124.05084 136544.0 2304 124.05084 136544.0
2305 129.05762 234973.0 2305 129.05762 234973.0
2306 130.06567 646047.0 2306 130.06567 646047.0
2307 131.06102 64470.0 2307 131.06102 64470.0
2308 131.07352 162979.0 2308 131.07352 162979.0
2309 132.04504 124496.0 2309 132.04504 124496.0
2310 132.06866 204911.0 2310 132.06866 204911.0
2311 135.04469 1656891.0 2311 135.04469 1656891.0
2312 136.05099 82782.0 2312 136.05099 82782.0
2313 137.05911 95506.0 2313 137.05911 95506.0
2314 138.06671 5569473.0 2314 138.06671 5569473.0
2315 139.0507 103856.0 2315 139.0507 103856.0
2316 141.05769 86459.0 2316 141.05769 86459.0
2317 142.05298 63910.0 2317 142.05298 63910.0
2318 142.0657 196862.0 2318 142.0657 196862.0
2319 143.06068 233150.0 2319 143.06068 233150.0
2320 143.07355 214610.0 2320 143.07355 214610.0
2321 144.0448 925002.0 2321 144.0448 925002.0
2322 144.06847 64229.0 2322 144.06847 64229.0
2323 144.08099 258802.0 2323 144.08099 258802.0
2324 145.0527 116335.0 2324 145.0527 116335.0
2325 145.06537 86828.0 2325 145.06537 86828.0
2326 145.07661 796518.0 2326 145.07661 796518.0
2327 146.06033 143788.0 2327 146.06033 143788.0
2328 146.08401 227348.0 2328 146.08401 227348.0
2329 155.04976 327910.0 2329 155.04976 327910.0
2330 155.06065 279544.0 2330 155.06065 279544.0
2331 156.06877 75745.0 2331 156.06877 75745.0
2332 157.05295 67758.0 2332 157.05295 67758.0
2333 157.0614 631707.0 2333 157.0614 631707.0
2334 157.0762 440265.0 2334 157.0762 440265.0
2335 158.06033 63862.0 2335 158.06033 63862.0
2336 158.08434 1135306.0 2336 158.08434 1135306.0
2337 159.06828 1092296.0 2337 159.06828 1092296.0
2338 159.09198 191557.0 2338 159.09198 191557.0
2339 160.07613 68662.0 2339 160.07613 68662.0
2340 169.07677 248853.0 2340 169.07677 248853.0
2341 170.06049 475510.0 2341 170.06049 475510.0
2342 170.0843 65958.0 2342 170.0843 65958.0
2343 171.05582 124587.0 2343 171.05582 124587.0
2344 171.09184 186652.0 2344 171.09184 186652.0
2345 172.07626 63322.0 2345 172.07626 63322.0
2346 172.08717 90299.0 2346 172.08717 90299.0
2347 173.07166 613565.0 2347 173.07166 613565.0
2348 174.07939 186701.0 2348 174.07939 186701.0
2349 174.10281 124566.0 2349 174.10281 124566.0
2350 183.0555 60224.0 2350 183.0555 60224.0
2351 185.0714 282332.0 2351 185.0714 282332.0
2352 186.05576 83272.0 2352 186.05576 83272.0
2353 186.10275 837404.0 2353 186.10275 837404.0
2354 187.08711 307005.0 2354 187.08711 307005.0
2355 187.11115 179545.0 2355 187.11115 179545.0
2356 188.08208 68182.0 2356 188.08208 68182.0
2357 188.09454 56664.0 2357 188.09454 56664.0
2358 189.10245 172485.0 2358 189.10245 172485.0
2359 197.0715 161124.0 2359 197.0715 161124.0
2360 198.07919 265419.0 2360 198.07919 265419.0
2361 199.07426 148687.0 2361 199.07426 148687.0
2362 199.08707 368116.0 2362 199.08707 368116.0
2363 200.08215 638373.0 2363 200.08215 638373.0
2364 201.10309 239504.0 2364 201.10309 239504.0
2365 202.09793 790032.0 2365 202.09793 790032.0
2366 214.09836 4878472.0 2366 214.09836 4878472.0
2367 215.10576 1548726.0 2367 215.10576 1548726.0
2368 230.09335 285190.0 2368 230.09335 285190.0
2369 231.10078 772223.0 2369 231.10078 772223.0
2370 366.14682 271014.0 2370 366.14682 271014.0
2371 2371
2372 COMPOUND_NAME: Flonicamid
2372 SCANNUMBER: 1609 2373 SCANNUMBER: 1609
2373 IONMODE: Positive 2374 IONMODE: Positive
2374 SPECTRUMTYPE: Centroid 2375 SPECTRUMTYPE: Centroid
2375 FORMULA: C9H6N3OF3 2376 FORMULA: C9H6N3OF3
2376 INCHIKEY: RLQJEEJISHYWON-UHFFFAOYSA-N 2377 INCHIKEY: RLQJEEJISHYWON-UHFFFAOYSA-N
2379 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2380 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2380 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2381 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2381 IONIZATION: ESI+ 2382 IONIZATION: ESI+
2382 LICENSE: CC BY-NC 2383 LICENSE: CC BY-NC
2383 COMMENT: 2384 COMMENT:
2384 COMPOUND_NAME: Flonicamid
2385 RETENTION_TIME: 1.603478 2385 RETENTION_TIME: 1.603478
2386 PRECURSOR_MZ: 230.054 2386 PRECURSOR_MZ: 230.054
2387 ADDUCT: [M+H]+ 2387 ADDUCT: [M+H]+
2388 COLLISION_ENERGY: 2388 COLLISION_ENERGY:
2389 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2389 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2390 NUM PEAKS: 22 2390 NUM PEAKS: 22
2391 98.04052 1513015.0 2391 98.04052 1513015.0
2392 101.01998 130358.0 2392 101.01998 130358.0
2393 126.03515 270418.0 2393 126.03515 270418.0
2394 128.0309 1130827.0 2394 128.0309 1130827.0
2395 129.03873 894240.0 2395 129.03873 894240.0
2396 134.04785 187862.0 2396 134.04785 187862.0
2397 135.03584 106359.0 2397 135.03584 106359.0
2398 136.04333 85854.0 2398 136.04333 85854.0
2399 140.03102 72212.0 2399 140.03102 72212.0
2400 144.02579 576288.0 2400 144.02579 576288.0
2401 146.02148 1739781.0 2401 146.02148 1739781.0
2402 147.02966 723489.0 2402 147.02966 723489.0
2403 148.03722 5717933.0 2403 148.03722 5717933.0
2404 153.04604 178370.0 2404 153.04604 178370.0
2405 155.04199 750642.0 2405 155.04199 750642.0
2406 156.02586 62411.0 2406 156.02586 62411.0
2407 164.03217 431199.0 2407 164.03217 431199.0
2408 174.01654 1374723.0 2408 174.01654 1374723.0
2409 175.0481 152887.0 2409 175.0481 152887.0
2410 176.0318 1685318.0 2410 176.0318 1685318.0
2411 183.0369 1014810.0 2411 183.0369 1014810.0
2412 203.04269 761411.0 2412 203.04269 761411.0
2413 2413
2414 COMPOUND_NAME: Fluoxastrobin
2414 SCANNUMBER: 7721 2415 SCANNUMBER: 7721
2415 IONMODE: Positive 2416 IONMODE: Positive
2416 SPECTRUMTYPE: Centroid 2417 SPECTRUMTYPE: Centroid
2417 FORMULA: C21H16N4O5ClF 2418 FORMULA: C21H16N4O5ClF
2418 INCHIKEY: UFEODZBUAFNAEU-UHFFFAOYSA-N 2419 INCHIKEY: UFEODZBUAFNAEU-UHFFFAOYSA-N
2421 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2422 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2422 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2423 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2423 IONIZATION: ESI+ 2424 IONIZATION: ESI+
2424 LICENSE: CC BY-NC 2425 LICENSE: CC BY-NC
2425 COMMENT: 2426 COMMENT:
2426 COMPOUND_NAME: Fluoxastrobin
2427 RETENTION_TIME: 7.061409 2427 RETENTION_TIME: 7.061409
2428 PRECURSOR_MZ: 459.0882 2428 PRECURSOR_MZ: 459.0882
2429 ADDUCT: [M+H]+ 2429 ADDUCT: [M+H]+
2430 COLLISION_ENERGY: 2430 COLLISION_ENERGY:
2431 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2431 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2432 NUM PEAKS: 85 2432 NUM PEAKS: 85
2433 90.03426 262008.0 2433 90.03426 262008.0
2434 93.0339 81235.0 2434 93.0339 81235.0
2435 95.04953 126363.0 2435 95.04953 126363.0
2436 104.04984 132927.0 2436 104.04984 132927.0
2437 105.04505 96553.0 2437 105.04505 96553.0
2438 106.02911 119639.0 2438 106.02911 119639.0
2439 111.04436 132213.0 2439 111.04436 132213.0
2440 118.05279 109270.0 2440 118.05279 109270.0
2441 119.03689 143696.0 2441 119.03689 143696.0
2442 120.04464 501451.0 2442 120.04464 501451.0
2443 122.04026 150489.0 2443 122.04026 150489.0
2444 129.01041 330269.0 2444 129.01041 330269.0
2445 129.04503 292390.0 2445 129.04503 292390.0
2446 130.02905 326516.0 2446 130.02905 326516.0
2447 130.04021 649052.0 2447 130.04021 649052.0
2448 132.04463 118853.0 2448 132.04463 118853.0
2449 134.04034 93930.0 2449 134.04034 93930.0
2450 138.011 2207225.0 2450 138.011 2207225.0
2451 138.99483 184424.0 2451 138.99483 184424.0
2452 139.00627 992155.0 2452 139.00627 992155.0
2453 144.03229 102927.0 2453 144.03229 102927.0
2454 145.04005 956703.0 2454 145.04005 956703.0
2455 150.03526 1178492.0 2455 150.03526 1178492.0
2456 151.00616 106379.0 2456 151.00616 106379.0
2457 154.04019 85122.0 2457 154.04019 85122.0
2458 157.04028 88434.0 2458 157.04028 88434.0
2459 159.036 96008.0 2459 159.036 96008.0
2460 160.02722 141264.0 2460 160.02722 141264.0
2461 160.04352 103289.0 2461 160.04352 103289.0
2462 161.03488 323066.0 2462 161.03488 323066.0
2463 162.03548 140596.0 2463 162.03548 140596.0
2464 162.04268 203634.0 2464 162.04268 203634.0
2465 162.0554 114359.0 2465 162.0554 114359.0
2466 163.00633 194952.0 2466 163.00633 194952.0
2467 163.05046 168483.0 2467 163.05046 168483.0
2468 164.03441 768408.0 2468 164.03441 768408.0
2469 168.00159 464518.0 2469 168.00159 464518.0
2470 170.03549 190735.0 2470 170.03549 190735.0
2471 175.03069 390492.0 2471 175.03069 390492.0
2472 176.0387 156295.0 2472 176.0387 156295.0
2473 178.02998 1064297.0 2473 178.02998 1064297.0
2474 179.00104 397625.0 2474 179.00104 397625.0
2475 183.99632 171687.0 2475 183.99632 171687.0
2476 188.03847 7591765.0 2476 188.03847 7591765.0
2477 188.05785 92062.0 2477 188.05785 92062.0
2478 189.04591 91704.0 2478 189.04591 91704.0
2479 190.04181 129380.0 2479 190.04181 129380.0
2480 191.02574 180590.0 2480 191.02574 180590.0
2481 202.04166 121581.0 2481 202.04166 121581.0
2482 205.04123 347646.0 2482 205.04123 347646.0
2483 205.06093 241613.0 2483 205.06093 241613.0
2484 214.00674 231209.0 2484 214.00674 231209.0
2485 214.0412 97985.0 2485 214.0412 97985.0
2486 216.05721 78878.0 2486 216.05721 78878.0
2487 218.03612 98376.0 2487 218.03612 98376.0
2488 223.00748 102872.0 2488 223.00748 102872.0
2489 223.9912 115573.0 2489 223.9912 115573.0
2490 225.05933 90781.0 2490 225.05933 90781.0
2491 228.04449 112509.0 2491 228.04449 112509.0
2492 229.02827 136264.0 2492 229.02827 136264.0
2493 230.03622 724472.0 2493 230.03622 724472.0
2494 240.04454 142077.0 2494 240.04454 142077.0
2495 241.05283 128789.0 2495 241.05283 128789.0
2496 244.05261 88750.0 2496 244.05261 88750.0
2497 246.0312 274116.0 2497 246.0312 274116.0
2498 251.06181 83031.0 2498 251.06181 83031.0
2499 252.06947 77596.0 2499 252.06947 77596.0
2500 255.03178 103007.0 2500 255.03178 103007.0
2501 257.04721 91609.0 2501 257.04721 91609.0
2502 266.01273 226670.0 2502 266.01273 226670.0
2503 274.06223 117152.0 2503 274.06223 117152.0
2504 277.06509 115503.0 2504 277.06509 115503.0
2505 278.07285 221625.0 2505 278.07285 221625.0
2506 279.05734 137186.0 2506 279.05734 137186.0
2507 280.06467 243149.0 2507 280.06467 243149.0
2508 304.0531 127719.0 2508 304.0531 127719.0
2509 306.0679 3047910.0 2509 306.0679 3047910.0
2510 313.04251 87383.0 2510 313.04251 87383.0
2511 315.03339 303129.0 2511 315.03339 303129.0
2512 318.06851 266951.0 2512 318.06851 266951.0
2513 331.0636 304000.0 2513 331.0636 304000.0
2514 340.02972 444209.0 2514 340.02972 444209.0
2515 342.04449 118004.0 2515 342.04449 118004.0
2516 367.03973 216560.0 2516 367.03973 216560.0
2517 383.03424 104628.0 2517 383.03424 104628.0
2518 2518
2519 COMPOUND_NAME: Flutolanil
2519 SCANNUMBER: 3979 2520 SCANNUMBER: 3979
2520 IONMODE: Positive 2521 IONMODE: Positive
2521 SPECTRUMTYPE: Centroid 2522 SPECTRUMTYPE: Centroid
2522 FORMULA: C17H16NO2F3 2523 FORMULA: C17H16NO2F3
2523 INCHIKEY: PTCGDEVVHUXTMP-UHFFFAOYSA-N 2524 INCHIKEY: PTCGDEVVHUXTMP-UHFFFAOYSA-N
2526 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2527 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2527 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2528 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2528 IONIZATION: ESI+ 2529 IONIZATION: ESI+
2529 LICENSE: CC BY-NC 2530 LICENSE: CC BY-NC
2530 COMMENT: 2531 COMMENT:
2531 COMPOUND_NAME: Flutolanil
2532 RETENTION_TIME: 6.193638 2532 RETENTION_TIME: 6.193638
2533 PRECURSOR_MZ: 324.1214 2533 PRECURSOR_MZ: 324.1214
2534 ADDUCT: [M+H]+ 2534 ADDUCT: [M+H]+
2535 COLLISION_ENERGY: 2535 COLLISION_ENERGY:
2536 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2536 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2537 NUM PEAKS: 12 2537 NUM PEAKS: 12
2538 111.04436 4020810.0 2538 111.04436 4020810.0
2539 121.03985 3392917.0 2539 121.03985 3392917.0
2540 130.02905 2402830.0 2540 130.02905 2402830.0
2541 145.02599 877135.0 2541 145.02599 877135.0
2542 166.06538 168609.0 2542 166.06538 168609.0
2543 173.02094 3306207.0 2543 173.02094 3306207.0
2544 194.0601 203214.0 2544 194.0601 203214.0
2545 214.06641 383897.0 2545 214.06641 383897.0
2546 222.05511 217155.0 2546 222.05511 217155.0
2547 242.05533 161728.0 2547 242.05533 161728.0
2548 242.06139 15929322.0 2548 242.06139 15929322.0
2549 262.06796 878870.0 2549 262.06796 878870.0
2550 2550
2551 COMPOUND_NAME: Furalaxyl
2551 SCANNUMBER: 3970 2552 SCANNUMBER: 3970
2552 IONMODE: Positive 2553 IONMODE: Positive
2553 SPECTRUMTYPE: Centroid 2554 SPECTRUMTYPE: Centroid
2554 FORMULA: C17H19NO4 2555 FORMULA: C17H19NO4
2555 INCHIKEY: CIEXPHRYOLIQQD-ZDUSSCGKSA-N 2556 INCHIKEY: CIEXPHRYOLIQQD-ZDUSSCGKSA-N
2558 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2559 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2559 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2560 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2560 IONIZATION: ESI+ 2561 IONIZATION: ESI+
2561 LICENSE: CC BY-NC 2562 LICENSE: CC BY-NC
2562 COMMENT: 2563 COMMENT:
2563 COMPOUND_NAME: Furalaxyl
2564 RETENTION_TIME: 6.193638 2564 RETENTION_TIME: 6.193638
2565 PRECURSOR_MZ: 302.1392 2565 PRECURSOR_MZ: 302.1392
2566 ADDUCT: [M+H]+ 2566 ADDUCT: [M+H]+
2567 COLLISION_ENERGY: 2567 COLLISION_ENERGY:
2568 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2568 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2569 NUM PEAKS: 1 2569 NUM PEAKS: 1
2570 95.01299 22120298.0 2570 95.01299 22120298.0
2571 2571
2572 COMPOUND_NAME: Imazalil
2572 SCANNUMBER: 2732 2573 SCANNUMBER: 2732
2573 IONMODE: Positive 2574 IONMODE: Positive
2574 SPECTRUMTYPE: Centroid 2575 SPECTRUMTYPE: Centroid
2575 FORMULA: C14H14N2OCl2 2576 FORMULA: C14H14N2OCl2
2576 INCHIKEY: PZBPKYOVPCNPJY-AWEZNQCLSA-N 2577 INCHIKEY: PZBPKYOVPCNPJY-AWEZNQCLSA-N
2579 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2580 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2580 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2581 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2581 IONIZATION: ESI+ 2582 IONIZATION: ESI+
2582 LICENSE: CC BY-NC 2583 LICENSE: CC BY-NC
2583 COMMENT: 2584 COMMENT:
2584 COMPOUND_NAME: Imazalil
2585 RETENTION_TIME: 3.913752 2585 RETENTION_TIME: 3.913752
2586 PRECURSOR_MZ: 297.0566 2586 PRECURSOR_MZ: 297.0566
2587 ADDUCT: [M+H]+ 2587 ADDUCT: [M+H]+
2588 COLLISION_ENERGY: 2588 COLLISION_ENERGY:
2589 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2589 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2590 NUM PEAKS: 17 2590 NUM PEAKS: 17
2591 102.04659 83349.0 2591 102.04659 83349.0
2592 109.0761 370634.0 2592 109.0761 370634.0
2593 122.99966 169161.0 2593 122.99966 169161.0
2594 129.07021 173674.0 2594 129.07021 173674.0
2595 137.01562 175055.0 2595 137.01562 175055.0
2596 138.02319 151710.0 2596 138.02319 151710.0
2597 141.0703 676682.0 2597 141.0703 676682.0
2598 149.01559 103927.0 2598 149.01559 103927.0
2599 150.02344 201572.0 2599 150.02344 201572.0
2600 158.97626 8128112.0 2600 158.97626 8128112.0
2601 164.03893 173925.0 2601 164.03893 173925.0
2602 172.99223 1736974.0 2602 172.99223 1736974.0
2603 175.03131 122074.0 2603 175.03131 122074.0
2604 176.0387 901695.0 2604 176.0387 901695.0
2605 186.97179 139839.0 2605 186.97179 139839.0
2606 200.98682 142186.0 2606 200.98682 142186.0
2607 255.00883 411510.0 2607 255.00883 411510.0
2608 2608
2609 COMPOUND_NAME: Imidacloprid
2609 SCANNUMBER: 2109 2610 SCANNUMBER: 2109
2610 IONMODE: Positive 2611 IONMODE: Positive
2611 SPECTRUMTYPE: Centroid 2612 SPECTRUMTYPE: Centroid
2612 FORMULA: C9H10N5O2Cl 2613 FORMULA: C9H10N5O2Cl
2613 INCHIKEY: YWTYJOPNNQFBPC-UHFFFAOYSA-N 2614 INCHIKEY: YWTYJOPNNQFBPC-UHFFFAOYSA-N
2616 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2617 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2617 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2618 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2618 IONIZATION: ESI+ 2619 IONIZATION: ESI+
2619 LICENSE: CC BY-NC 2620 LICENSE: CC BY-NC
2620 COMMENT: 2621 COMMENT:
2621 COMPOUND_NAME: Imidacloprid
2622 RETENTION_TIME: 3.079668 2622 RETENTION_TIME: 3.079668
2623 PRECURSOR_MZ: 256.0602 2623 PRECURSOR_MZ: 256.0602
2624 ADDUCT: [M+H]+ 2624 ADDUCT: [M+H]+
2625 COLLISION_ENERGY: 2625 COLLISION_ENERGY:
2626 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2626 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2627 NUM PEAKS: 36 2627 NUM PEAKS: 36
2628 99.05553 45726.0 2628 99.05553 45726.0
2629 105.04505 49039.0 2629 105.04505 49039.0
2630 106.06546 54345.0 2630 106.06546 54345.0
2631 107.06065 64812.0 2631 107.06065 64812.0
2632 113.00283 42520.0 2632 113.00283 42520.0
2633 119.04804 44604.0 2633 119.04804 44604.0
2634 119.06059 69901.0 2634 119.06059 69901.0
2635 120.05593 48869.0 2635 120.05593 48869.0
2636 126.01085 269914.0 2636 126.01085 269914.0
2637 127.01869 53555.0 2637 127.01869 53555.0
2638 128.02625 263416.0 2638 128.02625 263416.0
2639 131.06062 65155.0 2639 131.06062 65155.0
2640 132.05562 39478.0 2640 132.05562 39478.0
2641 133.06364 158210.0 2641 133.06364 158210.0
2642 133.076 126641.0 2642 133.076 126641.0
2643 134.07159 138270.0 2643 134.07159 138270.0
2644 141.02173 133666.0 2644 141.02173 133666.0
2645 146.05891 66316.0 2645 146.05891 66316.0
2646 146.0717 317182.0 2646 146.0717 317182.0
2647 147.06651 418911.0 2647 147.06651 418911.0
2648 148.08702 165957.0 2648 148.08702 165957.0
2649 158.07153 211685.0 2649 158.07153 211685.0
2650 159.06667 39062.0 2650 159.06667 39062.0
2651 159.07906 265140.0 2651 159.07906 265140.0
2652 166.01717 43422.0 2652 166.01717 43422.0
2653 167.03738 137027.0 2653 167.03738 137027.0
2654 173.08266 507123.0 2654 173.08266 507123.0
2655 174.09048 481291.0 2655 174.09048 481291.0
2656 175.09782 2784924.0 2656 175.09782 2784924.0
2657 180.03256 49532.0 2657 180.03256 49532.0
2658 181.02791 160573.0 2658 181.02791 160573.0
2659 191.09306 100802.0 2659 191.09306 100802.0
2660 194.04849 73037.0 2660 194.04849 73037.0
2661 208.05171 91411.0 2661 208.05171 91411.0
2662 209.05724 1316587.0 2662 209.05724 1316587.0
2663 209.05885 3531093.0 2663 209.05885 3531093.0
2664 2664
2665 COMPOUND_NAME: Mandipropamid
2665 SCANNUMBER: 7168 2666 SCANNUMBER: 7168
2666 IONMODE: Positive 2667 IONMODE: Positive
2667 SPECTRUMTYPE: Centroid 2668 SPECTRUMTYPE: Centroid
2668 FORMULA: C23H22NO4Cl 2669 FORMULA: C23H22NO4Cl
2669 INCHIKEY: KWLVWJPJKJMCSH-JOCHJYFZSA-N 2670 INCHIKEY: KWLVWJPJKJMCSH-JOCHJYFZSA-N
2672 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2673 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2673 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2674 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2674 IONIZATION: ESI+ 2675 IONIZATION: ESI+
2675 LICENSE: CC BY-NC 2676 LICENSE: CC BY-NC
2676 COMMENT: 2677 COMMENT:
2677 COMPOUND_NAME: Mandipropamid
2678 RETENTION_TIME: 6.964275 2678 RETENTION_TIME: 6.964275
2679 PRECURSOR_MZ: 412.1314 2679 PRECURSOR_MZ: 412.1314
2680 ADDUCT: [M+H]+ 2680 ADDUCT: [M+H]+
2681 COLLISION_ENERGY: 2681 COLLISION_ENERGY:
2682 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2682 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2683 NUM PEAKS: 5 2683 NUM PEAKS: 5
2684 204.10207 530532.0 2684 204.10207 530532.0
2685 328.11053 16472820.0 2685 328.11053 16472820.0
2686 356.10495 7175862.0 2686 356.10495 7175862.0
2687 412.04471 215694.0 2687 412.04471 215694.0
2688 412.13226 2828841.0 2688 412.13226 2828841.0
2689 2689
2690 COMPOUND_NAME: Mepanipyrim
2690 SCANNUMBER: 7089 2691 SCANNUMBER: 7089
2691 IONMODE: Positive 2692 IONMODE: Positive
2692 SPECTRUMTYPE: Centroid 2693 SPECTRUMTYPE: Centroid
2693 FORMULA: C14H13N3 2694 FORMULA: C14H13N3
2694 INCHIKEY: CIFWZNRJIBNXRE-UHFFFAOYSA-N 2695 INCHIKEY: CIFWZNRJIBNXRE-UHFFFAOYSA-N
2697 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2698 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2698 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2699 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2699 IONIZATION: ESI+ 2700 IONIZATION: ESI+
2700 LICENSE: CC BY-NC 2701 LICENSE: CC BY-NC
2701 COMMENT: 2702 COMMENT:
2702 COMPOUND_NAME: Mepanipyrim
2703 RETENTION_TIME: 6.936112 2703 RETENTION_TIME: 6.936112
2704 PRECURSOR_MZ: 224.1185 2704 PRECURSOR_MZ: 224.1185
2705 ADDUCT: [M+H]+ 2705 ADDUCT: [M+H]+
2706 COLLISION_ENERGY: 2706 COLLISION_ENERGY:
2707 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2707 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2708 NUM PEAKS: 102 2708 NUM PEAKS: 102
2709 89.03882 517274.0 2709 89.03882 517274.0
2710 90.03403 2492239.0 2710 90.03403 2492239.0
2711 91.04182 279822.0 2711 91.04182 279822.0
2712 91.05441 689902.0 2712 91.05441 689902.0
2713 92.0498 1156467.0 2713 92.0498 1156467.0
2714 93.0575 1581720.0 2714 93.0575 1581720.0
2715 94.04169 907699.0 2715 94.04169 907699.0
2716 94.06544 4247548.0 2716 94.06544 4247548.0
2717 95.04928 7648441.0 2717 95.04928 7648441.0
2718 96.04461 836099.0 2718 96.04461 836099.0
2719 104.04984 9863130.0 2719 104.04984 9863130.0
2720 105.04505 4799141.0 2720 105.04505 4799141.0
2721 105.05748 280682.0 2721 105.05748 280682.0
2722 106.05285 481449.0 2722 106.05285 481449.0
2723 106.06546 21345988.0 2723 106.06546 21345988.0
2724 107.06065 1636304.0 2724 107.06065 1636304.0
2725 107.07314 792818.0 2725 107.07314 792818.0
2726 115.05464 3041902.0 2726 115.05464 3041902.0
2727 116.0497 1214108.0 2727 116.0497 1214108.0
2728 117.0574 623912.0 2728 117.0574 623912.0
2729 118.05279 352181.0 2729 118.05279 352181.0
2730 118.06553 2089902.0 2730 118.06553 2089902.0
2731 119.06059 6016274.0 2731 119.06059 6016274.0
2732 121.07632 4716914.0 2732 121.07632 4716914.0
2733 122.06017 546355.0 2733 122.06017 546355.0
2734 124.07606 570495.0 2734 124.07606 570495.0
2735 128.04958 351035.0 2735 128.04958 351035.0
2736 128.06239 268794.0 2736 128.06239 268794.0
2737 129.04503 342815.0 2737 129.04503 342815.0
2738 129.05762 223642.0 2738 129.05762 223642.0
2739 129.07021 809903.0 2739 129.07021 809903.0
2740 130.04021 505143.0 2740 130.04021 505143.0
2741 130.05293 226615.0 2741 130.05293 226615.0
2742 130.06528 631733.0 2742 130.06528 631733.0
2743 131.06062 6745162.0 2743 131.06062 6745162.0
2744 132.06825 1922003.0 2744 132.06825 1922003.0
2745 139.05466 759207.0 2745 139.05466 759207.0
2746 139.08679 888214.0 2746 139.08679 888214.0
2747 140.0497 2660486.0 2747 140.0497 2660486.0
2748 141.05769 432867.0 2748 141.05769 432867.0
2749 142.06525 4535240.0 2749 142.06525 4535240.0
2750 143.06068 6551342.0 2750 143.06068 6551342.0
2751 143.07307 827696.0 2751 143.07307 827696.0
2752 146.06033 239932.0 2752 146.06033 239932.0
2753 146.0717 582762.0 2753 146.0717 582762.0
2754 147.07945 1981982.0 2754 147.07945 1981982.0
2755 149.07127 472905.0 2755 149.07127 472905.0
2756 152.06248 907036.0 2756 152.06248 907036.0
2757 153.06992 747588.0 2757 153.06992 747588.0
2758 154.06532 634466.0 2758 154.06532 634466.0
2759 155.06065 477098.0 2759 155.06065 477098.0
2760 156.06825 343240.0 2760 156.06825 343240.0
2761 156.08081 938982.0 2761 156.08081 938982.0
2762 157.0762 689823.0 2762 157.0762 689823.0
2763 157.08888 215289.0 2763 157.08888 215289.0
2764 158.08434 241364.0 2764 158.08434 241364.0
2765 159.09198 967686.0 2765 159.09198 967686.0
2766 160.07613 1334605.0 2766 160.07613 1334605.0
2767 165.05745 274138.0 2767 165.05745 274138.0
2768 166.06538 1659086.0 2768 166.06538 1659086.0
2769 167.06058 783829.0 2769 167.06058 783829.0
2770 167.07332 1978108.0 2770 167.07332 1978108.0
2771 168.06824 5290008.0 2771 168.06824 5290008.0
2772 168.08109 220063.0 2772 168.08109 220063.0
2773 169.06438 286507.0 2773 169.06438 286507.0
2774 169.07619 592750.0 2774 169.07619 592750.0
2775 170.0968 225887.0 2775 170.0968 225887.0
2776 178.06569 490619.0 2776 178.06569 490619.0
2777 179.06082 272597.0 2777 179.06082 272597.0
2778 179.07304 1573880.0 2778 179.07304 1573880.0
2779 180.08119 4503916.0 2779 180.08119 4503916.0
2780 181.07629 4276790.0 2780 181.07629 4276790.0
2781 181.08871 558180.0 2781 181.08871 558180.0
2782 182.08427 8178091.0 2782 182.08427 8178091.0
2783 182.09682 299282.0 2783 182.09682 299282.0
2784 183.07944 1118528.0 2784 183.07944 1118528.0
2785 183.09206 3652070.0 2785 183.09206 3652070.0
2786 184.08746 3084619.0 2786 184.08746 3084619.0
2787 184.09952 366883.0 2787 184.09952 366883.0
2788 185.0714 378043.0 2788 185.0714 378043.0
2789 190.06572 671329.0 2789 190.06572 671329.0
2790 191.06046 256444.0 2790 191.06046 256444.0
2791 191.07323 287427.0 2791 191.07323 287427.0
2792 192.06876 5238670.0 2792 192.06876 5238670.0
2793 193.07642 340761.0 2793 193.07642 340761.0
2794 194.0717 335171.0 2794 194.0717 335171.0
2795 194.08405 455850.0 2795 194.08405 455850.0
2796 195.09225 1664615.0 2796 195.09225 1664615.0
2797 196.0995 1003846.0 2797 196.0995 1003846.0
2798 197.09528 319437.0 2798 197.09528 319437.0
2799 197.10789 734438.0 2799 197.10789 734438.0
2800 205.07669 7605397.0 2800 205.07669 7605397.0
2801 206.08452 12079029.0 2801 206.08452 12079029.0
2802 207.0798 627312.0 2802 207.0798 627312.0
2803 207.0918 5892684.0 2803 207.0918 5892684.0
2804 208.08714 6327165.0 2804 208.08714 6327165.0
2805 208.09923 895713.0 2805 208.09923 895713.0
2806 209.09537 7619410.0 2806 209.09537 7619410.0
2807 221.09558 532629.0 2807 221.09558 532629.0
2808 222.10307 5281894.0 2808 222.10307 5281894.0
2809 223.11121 2054946.0 2809 223.11121 2054946.0
2810 224.119 13923746.0 2810 224.119 13923746.0
2811 2811
2812 COMPOUND_NAME: Dinotefuran
2812 SCANNUMBER: 1471 2813 SCANNUMBER: 1471
2813 IONMODE: Positive 2814 IONMODE: Positive
2814 SPECTRUMTYPE: Centroid 2815 SPECTRUMTYPE: Centroid
2815 FORMULA: C7H14N4O3 2816 FORMULA: C7H14N4O3
2816 INCHIKEY: YKBZOVFACRVRJN-ZCFIWIBFSA-N 2817 INCHIKEY: YKBZOVFACRVRJN-ZCFIWIBFSA-N
2819 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2820 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2820 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2821 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2821 IONIZATION: ESI+ 2822 IONIZATION: ESI+
2822 LICENSE: CC BY-NC 2823 LICENSE: CC BY-NC
2823 COMMENT: 2824 COMMENT:
2824 COMPOUND_NAME: Dinotefuran
2825 RETENTION_TIME: 1.502809 2825 RETENTION_TIME: 1.502809
2826 PRECURSOR_MZ: 203.1141 2826 PRECURSOR_MZ: 203.1141
2827 ADDUCT: [M+H]+ 2827 ADDUCT: [M+H]+
2828 COLLISION_ENERGY: 2828 COLLISION_ENERGY:
2829 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2829 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2830 NUM PEAKS: 13 2830 NUM PEAKS: 13
2831 87.07939 212770.0 2831 87.07939 212770.0
2832 100.0872 147065.0 2832 100.0872 147065.0
2833 101.09495 14292.0 2833 101.09495 14292.0
2834 112.08705 103076.0 2834 112.08705 103076.0
2835 113.09509 522233.0 2835 113.09509 522233.0
2836 114.10273 536607.0 2836 114.10273 536607.0
2837 127.11057 50518.0 2837 127.11057 50518.0
2838 128.11842 69200.0 2838 128.11842 69200.0
2839 129.08989 1106553.0 2839 129.08989 1106553.0
2840 129.12611 128089.0 2840 129.12611 128089.0
2841 157.12112 345152.0 2841 157.12112 345152.0
2842 173.11627 46987.0 2842 173.11627 46987.0
2843 203.11415 399504.0 2843 203.11415 399504.0
2844 2844
2845 COMPOUND_NAME: Metaflumizone
2845 SCANNUMBER: 8648 2846 SCANNUMBER: 8648
2846 IONMODE: Positive 2847 IONMODE: Positive
2847 SPECTRUMTYPE: Centroid 2848 SPECTRUMTYPE: Centroid
2848 FORMULA: C24H16N4O2F6 2849 FORMULA: C24H16N4O2F6
2849 INCHIKEY: MIFOMMKAVSCNKQ-UHFFFAOYSA-N 2850 INCHIKEY: MIFOMMKAVSCNKQ-UHFFFAOYSA-N
2852 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2853 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2853 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2854 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2854 IONIZATION: ESI+ 2855 IONIZATION: ESI+
2855 LICENSE: CC BY-NC 2856 LICENSE: CC BY-NC
2856 COMMENT: 2857 COMMENT:
2857 COMPOUND_NAME: Metaflumizone
2858 RETENTION_TIME: 7.19479 2858 RETENTION_TIME: 7.19479
2859 PRECURSOR_MZ: 507.1251 2859 PRECURSOR_MZ: 507.1251
2860 ADDUCT: [M+H]+ 2860 ADDUCT: [M+H]+
2861 COLLISION_ENERGY: 2861 COLLISION_ENERGY:
2862 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2862 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2863 NUM PEAKS: 33 2863 NUM PEAKS: 33
2864 89.03882 112603.0 2864 89.03882 112603.0
2865 92.0498 159120.0 2865 92.0498 159120.0
2866 93.0575 96261.0 2866 93.0575 96261.0
2867 110.06045 137716.0 2867 110.06045 137716.0
2868 116.0497 2188022.0 2868 116.0497 2188022.0
2869 128.04958 82526.0 2869 128.04958 82526.0
2870 159.04192 72170.0 2870 159.04192 72170.0
2871 171.04201 111513.0 2871 171.04201 111513.0
2872 174.05289 67561.0 2872 174.05289 67561.0
2873 176.03242 127986.0 2873 176.03242 127986.0
2874 177.04025 145377.0 2874 177.04025 145377.0
2875 178.04784 4081576.0 2875 178.04784 4081576.0
2876 190.065 44917.0 2876 190.065 44917.0
2877 191.07323 105042.0 2877 191.07323 105042.0
2878 204.02695 55744.0 2878 204.02695 55744.0
2879 218.08452 1276107.0 2879 218.08452 1276107.0
2880 219.09236 53088.0 2880 219.09236 53088.0
2881 220.05638 42611.0 2881 220.05638 42611.0
2882 221.05324 329863.0 2882 221.05324 329863.0
2883 233.05731 59799.0 2883 233.05731 59799.0
2884 238.06659 64784.0 2884 238.06659 64784.0
2885 240.06252 447032.0 2885 240.06252 447032.0
2886 245.07082 222043.0 2886 245.07082 222043.0
2887 247.06392 273902.0 2887 247.06392 273902.0
2888 247.06705 1414469.0 2888 247.06705 1414469.0
2889 260.0687 348712.0 2889 260.0687 348712.0
2890 267.07318 2569566.0 2890 267.07318 2569566.0
2891 273.06406 84541.0 2891 273.06406 84541.0
2892 273.07617 78440.0 2892 273.07617 78440.0
2893 286.07156 143270.0 2893 286.07156 143270.0
2894 287.07932 2154516.0 2894 287.07932 2154516.0
2895 288.0871 575359.0 2895 288.0871 575359.0
2896 330.08609 207585.0 2896 330.08609 207585.0
2897 2897
2898 COMPOUND_NAME: Metalaxyl
2898 SCANNUMBER: 3592 2899 SCANNUMBER: 3592
2899 IONMODE: Positive 2900 IONMODE: Positive
2900 SPECTRUMTYPE: Centroid 2901 SPECTRUMTYPE: Centroid
2901 FORMULA: C15H21NO4 2902 FORMULA: C15H21NO4
2902 INCHIKEY: ZQEIXNIJLIKNTD-LBPRGKRZSA-N 2903 INCHIKEY: ZQEIXNIJLIKNTD-LBPRGKRZSA-N
2905 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2906 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2906 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2907 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2907 IONIZATION: ESI+ 2908 IONIZATION: ESI+
2908 LICENSE: CC BY-NC 2909 LICENSE: CC BY-NC
2909 COMMENT: 2910 COMMENT:
2910 COMPOUND_NAME: Metalaxyl
2911 RETENTION_TIME: 5.550616 2911 RETENTION_TIME: 5.550616
2912 PRECURSOR_MZ: 280.1547 2912 PRECURSOR_MZ: 280.1547
2913 ADDUCT: [M+H]+ 2913 ADDUCT: [M+H]+
2914 COLLISION_ENERGY: 2914 COLLISION_ENERGY:
2915 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2915 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2916 NUM PEAKS: 24 2916 NUM PEAKS: 24
2917 91.05441 81742.0 2917 91.05441 81742.0
2918 105.06991 446715.0 2918 105.06991 446715.0
2919 117.0574 85397.0 2919 117.0574 85397.0
2920 118.06519 181419.0 2920 118.06519 181419.0
2921 119.0857 203031.0 2921 119.0857 203031.0
2922 120.081 86040.0 2922 120.081 86040.0
2923 121.08883 168662.0 2923 121.08883 168662.0
2924 130.06528 459915.0 2924 130.06528 459915.0
2925 131.0731 294735.0 2925 131.0731 294735.0
2926 132.08089 1629425.0 2926 132.08089 1629425.0
2927 133.08878 1053467.0 2927 133.08878 1053467.0
2928 134.09659 2186175.0 2928 134.09659 2186175.0
2929 144.08099 390383.0 2929 144.08099 390383.0
2930 145.08881 2412390.0 2930 145.08881 2412390.0
2931 146.09682 729220.0 2931 146.09682 729220.0
2932 147.10434 123350.0 2932 147.10434 123350.0
2933 148.11217 2255058.0 2933 148.11217 2255058.0
2934 150.09151 223495.0 2934 150.09151 223495.0
2935 158.0966 105904.0 2935 158.0966 105904.0
2936 160.11201 8036024.0 2936 160.11201 8036024.0
2937 162.12798 1800051.0 2937 162.12798 1800051.0
2938 164.10716 139534.0 2938 164.10716 139534.0
2939 192.13879 614235.0 2939 192.13879 614235.0
2940 220.13348 136200.0 2940 220.13348 136200.0
2941 2941
2942 COMPOUND_NAME: Myclobutanil
2942 SCANNUMBER: 4181 2943 SCANNUMBER: 4181
2943 IONMODE: Positive 2944 IONMODE: Positive
2944 SPECTRUMTYPE: Centroid 2945 SPECTRUMTYPE: Centroid
2945 FORMULA: C15H17N4Cl 2946 FORMULA: C15H17N4Cl
2946 INCHIKEY: HZJKXKUJVSEEFU-HNNXBMFYSA-N 2947 INCHIKEY: HZJKXKUJVSEEFU-HNNXBMFYSA-N
2949 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2950 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2950 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2951 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2951 IONIZATION: ESI+ 2952 IONIZATION: ESI+
2952 LICENSE: CC BY-NC 2953 LICENSE: CC BY-NC
2953 COMMENT: 2954 COMMENT:
2954 COMPOUND_NAME: Myclobutanil
2955 RETENTION_TIME: 6.259462 2955 RETENTION_TIME: 6.259462
2956 PRECURSOR_MZ: 289.1221 2956 PRECURSOR_MZ: 289.1221
2957 ADDUCT: [M+H]+ 2957 ADDUCT: [M+H]+
2958 COLLISION_ENERGY: 2958 COLLISION_ENERGY:
2959 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2959 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2960 NUM PEAKS: 18 2960 NUM PEAKS: 18
2961 89.03882 46919.0 2961 89.03882 46919.0
2962 98.99973 29039.0 2962 98.99973 29039.0
2963 115.05431 84807.0 2963 115.05431 84807.0
2964 116.06212 93918.0 2964 116.06212 93918.0
2965 125.01308 47666.0 2965 125.01308 47666.0
2966 125.01533 2894088.0 2966 125.01533 2894088.0
2967 128.04958 45144.0 2967 128.04958 45144.0
2968 130.06528 66651.0 2968 130.06528 66651.0
2969 137.01562 42490.0 2969 137.01562 42490.0
2970 149.01559 47429.0 2970 149.01559 47429.0
2971 150.0106 90969.0 2971 150.0106 90969.0
2972 151.03107 531808.0 2972 151.03107 531808.0
2973 153.06992 32172.0 2973 153.06992 32172.0
2974 164.02652 222253.0 2974 164.02652 222253.0
2975 166.04185 38601.0 2975 166.04185 38601.0
2976 168.09337 31175.0 2976 168.09337 31175.0
2977 175.03131 41390.0 2977 175.03131 41390.0
2978 178.04208 93247.0 2978 178.04208 93247.0
2979 2979
2980 COMPOUND_NAME: Oxadixyl
2980 SCANNUMBER: 3029 2981 SCANNUMBER: 3029
2981 IONMODE: Positive 2982 IONMODE: Positive
2982 SPECTRUMTYPE: Centroid 2983 SPECTRUMTYPE: Centroid
2983 FORMULA: C14H18N2O4 2984 FORMULA: C14H18N2O4
2984 INCHIKEY: UWVQIROCRJWDKL-UHFFFAOYSA-N 2985 INCHIKEY: UWVQIROCRJWDKL-UHFFFAOYSA-N
2987 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 2988 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
2988 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 2989 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
2989 IONIZATION: ESI+ 2990 IONIZATION: ESI+
2990 LICENSE: CC BY-NC 2991 LICENSE: CC BY-NC
2991 COMMENT: 2992 COMMENT:
2992 COMPOUND_NAME: Oxadixyl
2993 RETENTION_TIME: 4.402048 2993 RETENTION_TIME: 4.402048
2994 PRECURSOR_MZ: 279.1344 2994 PRECURSOR_MZ: 279.1344
2995 ADDUCT: [M+H]+ 2995 ADDUCT: [M+H]+
2996 COLLISION_ENERGY: 2996 COLLISION_ENERGY:
2997 INSTRUMENT_TYPE: LC-ESI-Orbitrap 2997 INSTRUMENT_TYPE: LC-ESI-Orbitrap
2998 NUM PEAKS: 7 2998 NUM PEAKS: 7
2999 102.05517 448694.0 2999 102.05517 448694.0
3000 132.08089 139055.0 3000 132.08089 139055.0
3001 133.08878 111093.0 3001 133.08878 111093.0
3002 160.07613 49235.0 3002 160.07613 49235.0
3003 192.10234 94587.0 3003 192.10234 94587.0
3004 219.11325 4470994.0 3004 219.11325 4470994.0
3005 279.13367 216370.0 3005 279.13367 216370.0
3006 3006
3007 COMPOUND_NAME: Prochloraz
3007 SCANNUMBER: 7968 3008 SCANNUMBER: 7968
3008 IONMODE: Positive 3009 IONMODE: Positive
3009 SPECTRUMTYPE: Centroid 3010 SPECTRUMTYPE: Centroid
3010 FORMULA: C15H16N3O2Cl3 3011 FORMULA: C15H16N3O2Cl3
3011 INCHIKEY: TVLSRXXIMLFWEO-UHFFFAOYSA-N 3012 INCHIKEY: TVLSRXXIMLFWEO-UHFFFAOYSA-N
3014 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3015 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3015 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3016 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3016 IONIZATION: ESI+ 3017 IONIZATION: ESI+
3017 LICENSE: CC BY-NC 3018 LICENSE: CC BY-NC
3018 COMMENT: 3019 COMMENT:
3019 COMPOUND_NAME: Prochloraz
3020 RETENTION_TIME: 7.089308 3020 RETENTION_TIME: 7.089308
3021 PRECURSOR_MZ: 376.0388 3021 PRECURSOR_MZ: 376.0388
3022 ADDUCT: [M+H]+ 3022 ADDUCT: [M+H]+
3023 COLLISION_ENERGY: 3023 COLLISION_ENERGY:
3024 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3024 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3025 NUM PEAKS: 3 3025 NUM PEAKS: 3
3026 265.95453 2776909.0 3026 265.95453 2776909.0
3027 308.00125 53942956.0 3027 308.00125 53942956.0
3028 376.03964 3704219.0 3028 376.03964 3704219.0
3029 3029
3030 COMPOUND_NAME: Prometon_1
3030 SCANNUMBER: 2214 3031 SCANNUMBER: 2214
3031 IONMODE: Positive 3032 IONMODE: Positive
3032 SPECTRUMTYPE: Centroid 3033 SPECTRUMTYPE: Centroid
3033 FORMULA: C10H19N5O 3034 FORMULA: C10H19N5O
3034 INCHIKEY: ISEUFVQQFVOBCY-UHFFFAOYSA-N 3035 INCHIKEY: ISEUFVQQFVOBCY-UHFFFAOYSA-N
3037 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3038 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3038 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3039 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3039 IONIZATION: ESI+ 3040 IONIZATION: ESI+
3040 LICENSE: CC BY-NC 3041 LICENSE: CC BY-NC
3041 COMMENT: 3042 COMMENT:
3042 COMPOUND_NAME: Prometon_1
3043 RETENTION_TIME: 3.185351 3043 RETENTION_TIME: 3.185351
3044 PRECURSOR_MZ: 226.1667 3044 PRECURSOR_MZ: 226.1667
3045 ADDUCT: [M+H]+ 3045 ADDUCT: [M+H]+
3046 COLLISION_ENERGY: 3046 COLLISION_ENERGY:
3047 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3047 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3048 NUM PEAKS: 16 3048 NUM PEAKS: 16
3049 85.05116 254026.0 3049 85.05116 254026.0
3050 85.07622 1248785.0 3050 85.07622 1248785.0
3051 86.03511 7693232.0 3051 86.03511 7693232.0
3052 96.05572 2045746.0 3052 96.05572 2045746.0
3053 97.03974 2776563.0 3053 97.03974 2776563.0
3054 99.06665 1175450.0 3054 99.06665 1175450.0
3055 100.05066 9824308.0 3055 100.05066 9824308.0
3056 110.04619 496522.0 3056 110.04619 496522.0
3057 110.0716 223643.0 3057 110.0716 223643.0
3058 114.06643 4195590.0 3058 114.06643 4195590.0
3059 128.08185 3094754.0 3059 128.08185 3094754.0
3060 138.07761 783556.0 3060 138.07761 783556.0
3061 142.07253 19868644.0 3061 142.07253 19868644.0
3062 168.0881 278497.0 3062 168.0881 278497.0
3063 170.10394 12296676.0 3063 170.10394 12296676.0
3064 184.11964 1858746.0 3064 184.11964 1858746.0
3065 3065
3066 COMPOUND_NAME: Prometon_2
3066 SCANNUMBER: 2376 3067 SCANNUMBER: 2376
3067 IONMODE: Positive 3068 IONMODE: Positive
3068 SPECTRUMTYPE: Centroid 3069 SPECTRUMTYPE: Centroid
3069 FORMULA: C10H19N5O 3070 FORMULA: C10H19N5O
3070 INCHIKEY: ISEUFVQQFVOBCY-UHFFFAOYSA-N 3071 INCHIKEY: ISEUFVQQFVOBCY-UHFFFAOYSA-N
3073 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3074 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3074 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3075 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3075 IONIZATION: ESI+ 3076 IONIZATION: ESI+
3076 LICENSE: CC BY-NC 3077 LICENSE: CC BY-NC
3077 COMMENT: 3078 COMMENT:
3078 COMPOUND_NAME: Prometon_2
3079 RETENTION_TIME: 3.288845 3079 RETENTION_TIME: 3.288845
3080 PRECURSOR_MZ: 226.1663 3080 PRECURSOR_MZ: 226.1663
3081 ADDUCT: [M+H]+ 3081 ADDUCT: [M+H]+
3082 COLLISION_ENERGY: 3082 COLLISION_ENERGY:
3083 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3083 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3084 NUM PEAKS: 22 3084 NUM PEAKS: 22
3085 85.05116 203704.0 3085 85.05116 203704.0
3086 85.07622 1795800.0 3086 85.07622 1795800.0
3087 86.03511 4360152.0 3087 86.03511 4360152.0
3088 96.05572 3992152.0 3088 96.05572 3992152.0
3089 97.03974 3296917.0 3089 97.03974 3296917.0
3090 99.06665 489124.0 3090 99.06665 489124.0
3091 100.05066 11922340.0 3091 100.05066 11922340.0
3092 110.04619 311190.0 3092 110.04619 311190.0
3093 110.0716 143123.0 3093 110.0716 143123.0
3094 113.0825 152844.0 3094 113.0825 152844.0
3095 114.06643 5615716.0 3095 114.06643 5615716.0
3096 125.0461 170765.0 3096 125.0461 170765.0
3097 127.09787 169642.0 3097 127.09787 169642.0
3098 128.08185 4145137.0 3098 128.08185 4145137.0
3099 129.0112 167032.0 3099 129.0112 167032.0
3100 138.07761 953215.0 3100 138.07761 953215.0
3101 142.07253 8482599.0 3101 142.07253 8482599.0
3102 153.07755 208846.0 3102 153.07755 208846.0
3103 168.0881 343548.0 3103 168.0881 343548.0
3104 170.10394 12923365.0 3104 170.10394 12923365.0
3105 184.11964 137608.0 3105 184.11964 137608.0
3106 226.16615 243943.0 3106 226.16615 243943.0
3107 3107
3108 COMPOUND_NAME: Pymetrozine
3108 SCANNUMBER: 1328 3109 SCANNUMBER: 1328
3109 IONMODE: Positive 3110 IONMODE: Positive
3110 SPECTRUMTYPE: Centroid 3111 SPECTRUMTYPE: Centroid
3111 FORMULA: C10H11N5O 3112 FORMULA: C10H11N5O
3112 INCHIKEY: QHMTXANCGGJZRX-UHFFFAOYSA-N 3113 INCHIKEY: QHMTXANCGGJZRX-UHFFFAOYSA-N
3115 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3116 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3116 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3117 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3117 IONIZATION: ESI+ 3118 IONIZATION: ESI+
3118 LICENSE: CC BY-NC 3119 LICENSE: CC BY-NC
3119 COMMENT: 3120 COMMENT:
3120 COMPOUND_NAME: Pymetrozine
3121 RETENTION_TIME: 1.373368 3121 RETENTION_TIME: 1.373368
3122 PRECURSOR_MZ: 218.1044 3122 PRECURSOR_MZ: 218.1044
3123 ADDUCT: [M+H]+ 3123 ADDUCT: [M+H]+
3124 COLLISION_ENERGY: 3124 COLLISION_ENERGY:
3125 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3125 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3126 NUM PEAKS: 2 3126 NUM PEAKS: 2
3127 96.04461 383408.0 3127 96.04461 383408.0
3128 105.04506 15166273.0 3128 105.04506 15166273.0
3129 3129
3130 COMPOUND_NAME: Pyracarbolid
3130 SCANNUMBER: 3243 3131 SCANNUMBER: 3243
3131 IONMODE: Positive 3132 IONMODE: Positive
3132 SPECTRUMTYPE: Centroid 3133 SPECTRUMTYPE: Centroid
3133 FORMULA: C13H15NO2 3134 FORMULA: C13H15NO2
3134 INCHIKEY: YPCALTGLHFLNGA-UHFFFAOYSA-N 3135 INCHIKEY: YPCALTGLHFLNGA-UHFFFAOYSA-N
3137 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3138 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3138 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3139 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3139 IONIZATION: ESI+ 3140 IONIZATION: ESI+
3140 LICENSE: CC BY-NC 3141 LICENSE: CC BY-NC
3141 COMMENT: 3142 COMMENT:
3142 COMPOUND_NAME: Pyracarbolid
3143 RETENTION_TIME: 4.72542 3143 RETENTION_TIME: 4.72542
3144 PRECURSOR_MZ: 218.1182 3144 PRECURSOR_MZ: 218.1182
3145 ADDUCT: [M+H]+ 3145 ADDUCT: [M+H]+
3146 COLLISION_ENERGY: 3146 COLLISION_ENERGY:
3147 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3147 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3148 NUM PEAKS: 8 3148 NUM PEAKS: 8
3149 92.04956 222486.0 3149 92.04956 222486.0
3150 95.04928 559755.0 3150 95.04928 559755.0
3151 97.02871 2882447.0 3151 97.02871 2882447.0
3152 97.06489 514552.0 3152 97.06489 514552.0
3153 105.04477 279492.0 3153 105.04477 279492.0
3154 107.04936 2653095.0 3154 107.04936 2653095.0
3155 115.03907 949155.0 3155 115.03907 949155.0
3156 125.05998 14590636.0 3156 125.05998 14590636.0
3157 3157
3158 COMPOUND_NAME: Pyrimethanil
3158 SCANNUMBER: 3684 3159 SCANNUMBER: 3684
3159 IONMODE: Positive 3160 IONMODE: Positive
3160 SPECTRUMTYPE: Centroid 3161 SPECTRUMTYPE: Centroid
3161 FORMULA: C12H13N3 3162 FORMULA: C12H13N3
3162 INCHIKEY: ZLIBICFPKPWGIZ-UHFFFAOYSA-N 3163 INCHIKEY: ZLIBICFPKPWGIZ-UHFFFAOYSA-N
3165 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3166 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3166 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3167 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3167 IONIZATION: ESI+ 3168 IONIZATION: ESI+
3168 LICENSE: CC BY-NC 3169 LICENSE: CC BY-NC
3169 COMMENT: 3170 COMMENT:
3170 COMPOUND_NAME: Pyrimethanil
3171 RETENTION_TIME: 5.598423 3171 RETENTION_TIME: 5.598423
3172 PRECURSOR_MZ: 200.1186 3172 PRECURSOR_MZ: 200.1186
3173 ADDUCT: [M+H]+ 3173 ADDUCT: [M+H]+
3174 COLLISION_ENERGY: 3174 COLLISION_ENERGY:
3175 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3175 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3176 NUM PEAKS: 43 3176 NUM PEAKS: 43
3177 91.05441 269141.0 3177 91.05441 269141.0
3178 92.0498 1006183.0 3178 92.0498 1006183.0
3179 93.0575 798806.0 3179 93.0575 798806.0
3180 95.04928 864623.0 3180 95.04928 864623.0
3181 105.04505 538940.0 3181 105.04505 538940.0
3182 107.06065 6806452.0 3182 107.06065 6806452.0
3183 115.05464 651194.0 3183 115.05464 651194.0
3184 116.0497 189558.0 3184 116.0497 189558.0
3185 117.0574 297627.0 3185 117.0574 297627.0
3186 118.05279 470418.0 3186 118.05279 470418.0
3187 118.06519 941436.0 3187 118.06519 941436.0
3188 119.06059 1862863.0 3188 119.06059 1862863.0
3189 125.07124 2658422.0 3189 125.07124 2658422.0
3190 129.07021 373721.0 3190 129.07021 373721.0
3191 131.06062 510426.0 3191 131.06062 510426.0
3192 132.08089 163131.0 3192 132.08089 163131.0
3193 139.05466 180641.0 3193 139.05466 180641.0
3194 140.0497 332716.0 3194 140.0497 332716.0
3195 141.05769 348146.0 3195 141.05769 348146.0
3196 142.06525 1271766.0 3196 142.06525 1271766.0
3197 143.06068 2584610.0 3197 143.06068 2584610.0
3198 143.07307 643411.0 3198 143.07307 643411.0
3199 154.06532 150404.0 3199 154.06532 150404.0
3200 155.06065 150810.0 3200 155.06065 150810.0
3201 156.06825 358067.0 3201 156.06825 358067.0
3202 156.08081 843618.0 3202 156.08081 843618.0
3203 158.08434 235445.0 3203 158.08434 235445.0
3204 158.0966 250403.0 3204 158.0966 250403.0
3205 159.09198 1057014.0 3205 159.09198 1057014.0
3206 166.06538 692025.0 3206 166.06538 692025.0
3207 167.07332 885398.0 3207 167.07332 885398.0
3208 168.06824 6869380.0 3208 168.06824 6869380.0
3209 173.10771 334158.0 3209 173.10771 334158.0
3210 173.50755 193551.0 3210 173.50755 193551.0
3211 181.07629 2021052.0 3211 181.07629 2021052.0
3212 182.08163 471666.0 3212 182.08163 471666.0
3213 182.08427 7602030.0 3213 182.08427 7602030.0
3214 183.09206 8147444.0 3214 183.09206 8147444.0
3215 184.08679 232595.0 3215 184.08679 232595.0
3216 185.09505 609372.0 3216 185.09505 609372.0
3217 198.10313 499158.0 3217 198.10313 499158.0
3218 199.11044 154902.0 3218 199.11044 154902.0
3219 200.11862 13352280.0 3219 200.11862 13352280.0
3220 3220
3221 COMPOUND_NAME: Pyriproxyfen
3221 SCANNUMBER: 10159 3222 SCANNUMBER: 10159
3222 IONMODE: Positive 3223 IONMODE: Positive
3223 SPECTRUMTYPE: Centroid 3224 SPECTRUMTYPE: Centroid
3224 FORMULA: C20H19NO3 3225 FORMULA: C20H19NO3
3225 INCHIKEY: NHDHVHZZCFYRSB-INIZCTEOSA-N 3226 INCHIKEY: NHDHVHZZCFYRSB-INIZCTEOSA-N
3228 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3229 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3229 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3230 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3230 IONIZATION: ESI+ 3231 IONIZATION: ESI+
3231 LICENSE: CC BY-NC 3232 LICENSE: CC BY-NC
3232 COMMENT: 3233 COMMENT:
3233 COMPOUND_NAME: Pyriproxyfen
3234 RETENTION_TIME: 7.483148 3234 RETENTION_TIME: 7.483148
3235 PRECURSOR_MZ: 322.1441 3235 PRECURSOR_MZ: 322.1441
3236 ADDUCT: [M+H]+ 3236 ADDUCT: [M+H]+
3237 COLLISION_ENERGY: 3237 COLLISION_ENERGY:
3238 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3238 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3239 NUM PEAKS: 21 3239 NUM PEAKS: 21
3240 91.05465 1995486.0 3240 91.05465 1995486.0
3241 95.04953 2794273.0 3241 95.04953 2794273.0
3242 96.04461 57722984.0 3242 96.04461 57722984.0
3243 105.04505 1487815.0 3243 105.04505 1487815.0
3244 105.0702 2138528.0 3244 105.0702 2138528.0
3245 115.05464 2166874.0 3245 115.05464 2166874.0
3246 119.04944 13154060.0 3246 119.04944 13154060.0
3247 128.06239 2789226.0 3247 128.06239 2789226.0
3248 129.07021 18069414.0 3248 129.07021 18069414.0
3249 133.06531 2250340.0 3249 133.06531 2250340.0
3250 134.07285 5007071.0 3250 134.07285 5007071.0
3251 141.07028 4802710.0 3251 141.07028 4802710.0
3252 153.07043 578116.0 3252 153.07043 578116.0
3253 155.06065 601649.0 3253 155.06065 601649.0
3254 157.06509 3489445.0 3254 157.06509 3489445.0
3255 170.07298 834102.0 3255 170.07298 834102.0
3256 181.06517 682957.0 3256 181.06517 682957.0
3257 185.05991 13867037.0 3257 185.05991 13867037.0
3258 186.06801 602621.0 3258 186.06801 602621.0
3259 194.07315 653455.0 3259 194.07315 653455.0
3260 199.07576 804230.0 3260 199.07576 804230.0
3261 3261
3262 COMPOUND_NAME: Mepronil
3262 SCANNUMBER: 5448 3263 SCANNUMBER: 5448
3263 IONMODE: Positive 3264 IONMODE: Positive
3264 SPECTRUMTYPE: Centroid 3265 SPECTRUMTYPE: Centroid
3265 FORMULA: C17H19NO2 3266 FORMULA: C17H19NO2
3266 INCHIKEY: BCTQJXQXJVLSIG-UHFFFAOYSA-N 3267 INCHIKEY: BCTQJXQXJVLSIG-UHFFFAOYSA-N
3269 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3270 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3270 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3271 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3271 IONIZATION: ESI+ 3272 IONIZATION: ESI+
3272 LICENSE: CC BY-NC 3273 LICENSE: CC BY-NC
3273 COMMENT: 3274 COMMENT:
3274 COMPOUND_NAME: Mepronil
3275 RETENTION_TIME: 6.63015 3275 RETENTION_TIME: 6.63015
3276 PRECURSOR_MZ: 270.1492 3276 PRECURSOR_MZ: 270.1492
3277 ADDUCT: [M+H]+ 3277 ADDUCT: [M+H]+
3278 COLLISION_ENERGY: 3278 COLLISION_ENERGY:
3279 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3279 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3280 NUM PEAKS: 8 3280 NUM PEAKS: 8
3281 91.05465 4818532.0 3281 91.05465 4818532.0
3282 107.04936 268915.0 3282 107.04936 268915.0
3283 108.0449 232011.0 3283 108.0449 232011.0
3284 109.0651 1528311.0 3284 109.0651 1528311.0
3285 111.04436 177960.0 3285 111.04436 177960.0
3286 119.04979 16405699.0 3286 119.04979 16405699.0
3287 119.0592 353581.0 3287 119.0592 353581.0
3288 136.03949 166339.0 3288 136.03949 166339.0
3289 3289
3290 COMPOUND_NAME: Spiroxamine_2
3290 SCANNUMBER: 3190 3291 SCANNUMBER: 3190
3291 IONMODE: Positive 3292 IONMODE: Positive
3292 SPECTRUMTYPE: Centroid 3293 SPECTRUMTYPE: Centroid
3293 FORMULA: C18H35NO2 3294 FORMULA: C18H35NO2
3294 INCHIKEY: PUYXTUJWRLOUCW-PQUAAJSLSA-N 3295 INCHIKEY: PUYXTUJWRLOUCW-PQUAAJSLSA-N
3297 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3298 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3298 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3299 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3299 IONIZATION: ESI+ 3300 IONIZATION: ESI+
3300 LICENSE: CC BY-NC 3301 LICENSE: CC BY-NC
3301 COMMENT: 3302 COMMENT:
3302 COMPOUND_NAME: Spiroxamine_2
3303 RETENTION_TIME: 4.628222 3303 RETENTION_TIME: 4.628222
3304 PRECURSOR_MZ: 298.2747 3304 PRECURSOR_MZ: 298.2747
3305 ADDUCT: [M+H]+ 3305 ADDUCT: [M+H]+
3306 COLLISION_ENERGY: 3306 COLLISION_ENERGY:
3307 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3307 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3308 NUM PEAKS: 4 3308 NUM PEAKS: 4
3309 100.11219 10585697.0 3309 100.11219 10585697.0
3310 102.09142 415934.0 3310 102.09142 415934.0
3311 126.12786 286929.0 3311 126.12786 286929.0
3312 144.13857 10367585.0 3312 144.13857 10367585.0
3313 3313
3314 COMPOUND_NAME: Tebufenpyrad
3314 SCANNUMBER: 8797 3315 SCANNUMBER: 8797
3315 IONMODE: Positive 3316 IONMODE: Positive
3316 SPECTRUMTYPE: Centroid 3317 SPECTRUMTYPE: Centroid
3317 FORMULA: C18H24N3OCl 3318 FORMULA: C18H24N3OCl
3318 INCHIKEY: ZZYSLNWGKKDOML-UHFFFAOYSA-N 3319 INCHIKEY: ZZYSLNWGKKDOML-UHFFFAOYSA-N
3321 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3322 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3322 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3323 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3323 IONIZATION: ESI+ 3324 IONIZATION: ESI+
3324 LICENSE: CC BY-NC 3325 LICENSE: CC BY-NC
3325 COMMENT: 3326 COMMENT:
3326 COMPOUND_NAME: Tebufenpyrad
3327 RETENTION_TIME: 7.223254 3327 RETENTION_TIME: 7.223254
3328 PRECURSOR_MZ: 334.1692 3328 PRECURSOR_MZ: 334.1692
3329 ADDUCT: [M+H]+ 3329 ADDUCT: [M+H]+
3330 COLLISION_ENERGY: 3330 COLLISION_ENERGY:
3331 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3331 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3332 NUM PEAKS: 17 3332 NUM PEAKS: 17
3333 90.01088 682936.0 3333 90.01088 682936.0
3334 91.05441 694638.0 3334 91.05441 694638.0
3335 105.0702 2926113.0 3335 105.0702 2926113.0
3336 107.08593 482744.0 3336 107.08593 482744.0
3337 117.02172 17275010.0 3337 117.02172 17275010.0
3338 117.06997 1213127.0 3338 117.06997 1213127.0
3339 119.0857 4335492.0 3339 119.0857 4335492.0
3340 130.02946 271510.0 3340 130.02946 271510.0
3341 131.08559 179894.0 3341 131.08559 179894.0
3342 132.09351 4494128.0 3342 132.09351 4494128.0
3343 145.05318 15327344.0 3343 145.05318 15327344.0
3344 145.10149 224176.0 3344 145.10149 224176.0
3345 147.11679 8812113.0 3345 147.11679 8812113.0
3346 171.03239 1499108.0 3346 171.03239 1499108.0
3347 188.05853 456215.0 3347 188.05853 456215.0
3348 200.05861 396435.0 3348 200.05861 396435.0
3349 334.16821 933979.0 3349 334.16821 933979.0
3350 3350
3351 COMPOUND_NAME: Terbumeton_1
3351 SCANNUMBER: 2214 3352 SCANNUMBER: 2214
3352 IONMODE: Positive 3353 IONMODE: Positive
3353 SPECTRUMTYPE: Centroid 3354 SPECTRUMTYPE: Centroid
3354 FORMULA: C10H19N5O 3355 FORMULA: C10H19N5O
3355 INCHIKEY: BCQMBFHBDZVHKU-UHFFFAOYSA-N 3356 INCHIKEY: BCQMBFHBDZVHKU-UHFFFAOYSA-N
3358 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3359 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3359 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3360 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3360 IONIZATION: ESI+ 3361 IONIZATION: ESI+
3361 LICENSE: CC BY-NC 3362 LICENSE: CC BY-NC
3362 COMMENT: 3363 COMMENT:
3363 COMPOUND_NAME: Terbumeton_1
3364 RETENTION_TIME: 3.185351 3364 RETENTION_TIME: 3.185351
3365 PRECURSOR_MZ: 226.1667 3365 PRECURSOR_MZ: 226.1667
3366 ADDUCT: [M+H]+ 3366 ADDUCT: [M+H]+
3367 COLLISION_ENERGY: 3367 COLLISION_ENERGY:
3368 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3368 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3369 NUM PEAKS: 16 3369 NUM PEAKS: 16
3370 85.05116 254026.0 3370 85.05116 254026.0
3371 85.07622 1248785.0 3371 85.07622 1248785.0
3372 86.03511 7693232.0 3372 86.03511 7693232.0
3373 96.05572 2045746.0 3373 96.05572 2045746.0
3374 97.03974 2776563.0 3374 97.03974 2776563.0
3375 99.06665 1175450.0 3375 99.06665 1175450.0
3376 100.05066 9824308.0 3376 100.05066 9824308.0
3377 110.04619 496522.0 3377 110.04619 496522.0
3378 110.0716 223643.0 3378 110.0716 223643.0
3379 114.06643 4195590.0 3379 114.06643 4195590.0
3380 128.08185 3094754.0 3380 128.08185 3094754.0
3381 138.07761 783556.0 3381 138.07761 783556.0
3382 142.07253 19868644.0 3382 142.07253 19868644.0
3383 168.0881 278497.0 3383 168.0881 278497.0
3384 170.10394 12296676.0 3384 170.10394 12296676.0
3385 184.11964 1858746.0 3385 184.11964 1858746.0
3386 3386
3387 COMPOUND_NAME: Terbumeton_2
3387 SCANNUMBER: 2376 3388 SCANNUMBER: 2376
3388 IONMODE: Positive 3389 IONMODE: Positive
3389 SPECTRUMTYPE: Centroid 3390 SPECTRUMTYPE: Centroid
3390 FORMULA: C10H19N5O 3391 FORMULA: C10H19N5O
3391 INCHIKEY: BCQMBFHBDZVHKU-UHFFFAOYSA-N 3392 INCHIKEY: BCQMBFHBDZVHKU-UHFFFAOYSA-N
3394 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3395 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3395 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3396 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3396 IONIZATION: ESI+ 3397 IONIZATION: ESI+
3397 LICENSE: CC BY-NC 3398 LICENSE: CC BY-NC
3398 COMMENT: 3399 COMMENT:
3399 COMPOUND_NAME: Terbumeton_2
3400 RETENTION_TIME: 3.288845 3400 RETENTION_TIME: 3.288845
3401 PRECURSOR_MZ: 226.1663 3401 PRECURSOR_MZ: 226.1663
3402 ADDUCT: [M+H]+ 3402 ADDUCT: [M+H]+
3403 COLLISION_ENERGY: 3403 COLLISION_ENERGY:
3404 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3404 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3405 NUM PEAKS: 22 3405 NUM PEAKS: 22
3406 85.05116 203704.0 3406 85.05116 203704.0
3407 85.07622 1795800.0 3407 85.07622 1795800.0
3408 86.03511 4360152.0 3408 86.03511 4360152.0
3409 96.05572 3992152.0 3409 96.05572 3992152.0
3410 97.03974 3296917.0 3410 97.03974 3296917.0
3411 99.06665 489124.0 3411 99.06665 489124.0
3412 100.05066 11922340.0 3412 100.05066 11922340.0
3413 110.04619 311190.0 3413 110.04619 311190.0
3414 110.0716 143123.0 3414 110.0716 143123.0
3415 113.0825 152844.0 3415 113.0825 152844.0
3416 114.06643 5615716.0 3416 114.06643 5615716.0
3417 125.0461 170765.0 3417 125.0461 170765.0
3418 127.09787 169642.0 3418 127.09787 169642.0
3419 128.08185 4145137.0 3419 128.08185 4145137.0
3420 129.0112 167032.0 3420 129.0112 167032.0
3421 138.07761 953215.0 3421 138.07761 953215.0
3422 142.07253 8482599.0 3422 142.07253 8482599.0
3423 153.07755 208846.0 3423 153.07755 208846.0
3424 168.0881 343548.0 3424 168.0881 343548.0
3425 170.10394 12923365.0 3425 170.10394 12923365.0
3426 184.11964 137608.0 3426 184.11964 137608.0
3427 226.16615 243943.0 3427 226.16615 243943.0
3428 3428
3429 COMPOUND_NAME: Triadimefon
3429 SCANNUMBER: 4753 3430 SCANNUMBER: 4753
3430 IONMODE: Positive 3431 IONMODE: Positive
3431 SPECTRUMTYPE: Centroid 3432 SPECTRUMTYPE: Centroid
3432 FORMULA: C14H16N3O2Cl 3433 FORMULA: C14H16N3O2Cl
3433 INCHIKEY: WURBVZBTWMNKQT-ZDUSSCGKSA-N 3434 INCHIKEY: WURBVZBTWMNKQT-ZDUSSCGKSA-N
3436 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3437 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3437 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3438 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3438 IONIZATION: ESI+ 3439 IONIZATION: ESI+
3439 LICENSE: CC BY-NC 3440 LICENSE: CC BY-NC
3440 COMMENT: 3441 COMMENT:
3441 COMPOUND_NAME: Triadimefon
3442 RETENTION_TIME: 6.495691 3442 RETENTION_TIME: 6.495691
3443 PRECURSOR_MZ: 294.101 3443 PRECURSOR_MZ: 294.101
3444 ADDUCT: [M+H]+ 3444 ADDUCT: [M+H]+
3445 COLLISION_ENERGY: 3445 COLLISION_ENERGY:
3446 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3446 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3447 NUM PEAKS: 34 3447 NUM PEAKS: 34
3448 91.05441 220380.0 3448 91.05441 220380.0
3449 93.03366 110759.0 3449 93.03366 110759.0
3450 94.04145 226678.0 3450 94.04145 226678.0
3451 95.04928 293143.0 3451 95.04928 293143.0
3452 98.99973 2161492.0 3452 98.99973 2161492.0
3453 103.03109 47635.0 3453 103.03109 47635.0
3454 105.04505 158971.0 3454 105.04505 158971.0
3455 107.04936 77343.0 3455 107.04936 77343.0
3456 109.0651 56624.0 3456 109.0651 56624.0
3457 110.03504 91263.0 3457 110.03504 91263.0
3458 110.99978 78358.0 3458 110.99978 78358.0
3459 111.04436 239293.0 3459 111.04436 239293.0
3460 113.0154 1133437.0 3460 113.0154 1133437.0
3461 119.04944 129126.0 3461 119.04944 129126.0
3462 119.06059 60561.0 3462 119.06059 60561.0
3463 120.05734 170448.0 3463 120.05734 170448.0
3464 121.03985 123630.0 3464 121.03985 123630.0
3465 125.01533 88037.0 3465 125.01533 88037.0
3466 126.99488 4331208.0 3466 126.99488 4331208.0
3467 127.03099 234800.0 3467 127.03099 234800.0
3468 129.01041 2984985.0 3468 129.01041 2984985.0
3469 133.10155 53571.0 3469 133.10155 53571.0
3470 137.01562 52817.0 3470 137.01562 52817.0
3471 139.00583 1903109.0 3471 139.00583 1903109.0
3472 141.0105 4051184.0 3472 141.0105 4051184.0
3473 146.07265 75724.0 3473 146.07265 75724.0
3474 147.08089 154110.0 3474 147.08089 154110.0
3475 155.02592 1609516.0 3475 155.02592 1609516.0
3476 159.02092 270169.0 3476 159.02092 270169.0
3477 161.09631 105167.0 3477 161.09631 105167.0
3478 173.50877 58953.0 3478 173.50877 58953.0
3479 175.07544 124355.0 3479 175.07544 124355.0
3480 190.09877 46793.0 3480 190.09877 46793.0
3481 197.073 124633.0 3481 197.073 124633.0
3482 3482
3483 COMPOUND_NAME: Trifloxystrobin
3483 SCANNUMBER: 8085 3484 SCANNUMBER: 8085
3484 IONMODE: Positive 3485 IONMODE: Positive
3485 SPECTRUMTYPE: Centroid 3486 SPECTRUMTYPE: Centroid
3486 FORMULA: C20H19N2O4F3 3487 FORMULA: C20H19N2O4F3
3487 INCHIKEY: ONCZDRURRATYFI-UHFFFAOYSA-N 3488 INCHIKEY: ONCZDRURRATYFI-UHFFFAOYSA-N
3490 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3491 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3491 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3492 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3492 IONIZATION: ESI+ 3493 IONIZATION: ESI+
3493 LICENSE: CC BY-NC 3494 LICENSE: CC BY-NC
3494 COMMENT: 3495 COMMENT:
3495 COMPOUND_NAME: Trifloxystrobin
3496 RETENTION_TIME: 7.117416 3496 RETENTION_TIME: 7.117416
3497 PRECURSOR_MZ: 409.1378 3497 PRECURSOR_MZ: 409.1378
3498 ADDUCT: [M+H]+ 3498 ADDUCT: [M+H]+
3499 COLLISION_ENERGY: 3499 COLLISION_ENERGY:
3500 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3500 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3501 NUM PEAKS: 20 3501 NUM PEAKS: 20
3502 89.03905 311273.0 3502 89.03905 311273.0
3503 91.05465 552137.0 3503 91.05465 552137.0
3504 105.07049 281496.0 3504 105.07049 281496.0
3505 116.05004 3644672.0 3505 116.05004 3644672.0
3506 117.05774 1059431.0 3506 117.05774 1059431.0
3507 118.06553 996646.0 3507 118.06553 996646.0
3508 119.04944 261371.0 3508 119.04944 261371.0
3509 130.06567 752094.0 3509 130.06567 752094.0
3510 131.07352 3968814.0 3510 131.07352 3968814.0
3511 132.04504 549533.0 3511 132.04504 549533.0
3512 132.08128 1313192.0 3512 132.08128 1313192.0
3513 134.06033 476020.0 3513 134.06033 476020.0
3514 145.02644 9201794.0 3514 145.02644 9201794.0
3515 146.06033 1786913.0 3515 146.06033 1786913.0
3516 147.06844 435652.0 3516 147.06844 435652.0
3517 161.0475 625467.0 3517 161.0475 625467.0
3518 163.03706 449951.0 3518 163.03706 449951.0
3519 173.03255 3885334.0 3519 173.03255 3885334.0
3520 186.05302 16153518.0 3520 186.05302 16153518.0
3521 206.08214 362046.0 3521 206.08214 362046.0
3522 3522
3523 COMPOUND_NAME: Zoxamide
3523 SCANNUMBER: 7511 3524 SCANNUMBER: 7511
3524 IONMODE: Positive 3525 IONMODE: Positive
3525 SPECTRUMTYPE: Centroid 3526 SPECTRUMTYPE: Centroid
3526 FORMULA: C14H16Cl3NO2 3527 FORMULA: C14H16Cl3NO2
3527 INCHIKEY: SOUGWDPPRBKJEX-AWEZNQCLSA-N 3528 INCHIKEY: SOUGWDPPRBKJEX-AWEZNQCLSA-N
3530 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3531 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3531 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3532 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3532 IONIZATION: ESI+ 3533 IONIZATION: ESI+
3533 LICENSE: CC BY-NC 3534 LICENSE: CC BY-NC
3534 COMMENT: 3535 COMMENT:
3535 COMPOUND_NAME: Zoxamide
3536 RETENTION_TIME: 7.042906 3536 RETENTION_TIME: 7.042906
3537 PRECURSOR_MZ: 336.0327 3537 PRECURSOR_MZ: 336.0327
3538 ADDUCT: [M+H]+ 3538 ADDUCT: [M+H]+
3539 COLLISION_ENERGY: 3539 COLLISION_ENERGY:
3540 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3540 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3541 NUM PEAKS: 7 3541 NUM PEAKS: 7
3542 122.99966 189624.0 3542 122.99966 189624.0
3543 158.97681 2350836.0 3543 158.97681 2350836.0
3544 160.99211 84080.0 3544 160.99211 84080.0
3545 176.98717 132424.0 3545 176.98717 132424.0
3546 186.97179 7551578.0 3546 186.97179 7551578.0
3547 186.98138 1310863.0 3547 186.98138 1310863.0
3548 203.99802 105210.0 3548 203.99802 105210.0
3549 3549
3550 COMPOUND_NAME: Quinoxyfen
3550 SCANNUMBER: 10658 3551 SCANNUMBER: 10658
3551 IONMODE: Positive 3552 IONMODE: Positive
3552 SPECTRUMTYPE: Centroid 3553 SPECTRUMTYPE: Centroid
3553 FORMULA: C15H8NOCl2F 3554 FORMULA: C15H8NOCl2F
3554 INCHIKEY: WRPIRSINYZBGPK-UHFFFAOYSA-N 3555 INCHIKEY: WRPIRSINYZBGPK-UHFFFAOYSA-N
3557 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3558 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3558 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3559 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3559 IONIZATION: ESI+ 3560 IONIZATION: ESI+
3560 LICENSE: CC BY-NC 3561 LICENSE: CC BY-NC
3561 COMMENT: 3562 COMMENT:
3562 COMPOUND_NAME: Quinoxyfen
3563 RETENTION_TIME: 7.693292 3563 RETENTION_TIME: 7.693292
3564 PRECURSOR_MZ: 308.0046 3564 PRECURSOR_MZ: 308.0046
3565 ADDUCT: [M+H]+ 3565 ADDUCT: [M+H]+
3566 COLLISION_ENERGY: 3566 COLLISION_ENERGY:
3567 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3567 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3568 NUM PEAKS: 28 3568 NUM PEAKS: 28
3569 113.04024 951160.0 3569 113.04024 951160.0
3570 123.00003 519051.0 3570 123.00003 519051.0
3571 123.03591 2234640.0 3571 123.03591 2234640.0
3572 133.05254 505534.0 3572 133.05254 505534.0
3573 150.01109 1173838.0 3573 150.01109 1173838.0
3574 162.01112 4388227.0 3574 162.01112 4388227.0
3575 168.02145 1536952.0 3575 168.02145 1536952.0
3576 178.01723 957090.0 3576 178.01723 957090.0
3577 183.97221 586345.0 3577 183.97221 586345.0
3578 184.97952 1042789.0 3578 184.97952 1042789.0
3579 196.98022 34758736.0 3579 196.98022 34758736.0
3580 209.06372 991608.0 3580 209.06372 991608.0
3581 210.0717 743797.0 3581 210.0717 743797.0
3582 212.97452 543051.0 3582 212.97452 543051.0
3583 213.98238 16892596.0 3583 213.98238 16892596.0
3584 217.02182 350576.0 3584 217.02182 350576.0
3585 219.02536 368183.0 3585 219.02536 368183.0
3586 225.03487 908834.0 3586 225.03487 908834.0
3587 237.05934 2476225.0 3587 237.05934 2476225.0
3588 238.06659 390133.0 3588 238.06659 390133.0
3589 244.03317 3467599.0 3589 244.03317 3467599.0
3590 245.04095 5069296.0 3590 245.04095 5069296.0
3591 253.02917 653474.0 3591 253.02917 653474.0
3592 254.03786 417640.0 3592 254.03786 417640.0
3593 272.02798 14312807.0 3593 272.02798 14312807.0
3594 280.00934 1380984.0 3594 280.00934 1380984.0
3595 287.99789 1053238.0 3595 287.99789 1053238.0
3596 308.00415 16622164.0 3596 308.00415 16622164.0
3597 3597
3598 COMPOUND_NAME: Rotenone
3598 SCANNUMBER: 10564 3599 SCANNUMBER: 10564
3599 IONMODE: Positive 3600 IONMODE: Positive
3600 SPECTRUMTYPE: Centroid 3601 SPECTRUMTYPE: Centroid
3601 FORMULA: C23H22O6 3602 FORMULA: C23H22O6
3602 INCHIKEY: JUVIOZPCNVVQFO-NDXORKPFSA-N 3603 INCHIKEY: JUVIOZPCNVVQFO-NDXORKPFSA-N
3605 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3606 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3606 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3607 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3607 IONIZATION: ESI+ 3608 IONIZATION: ESI+
3608 LICENSE: CC BY-NC 3609 LICENSE: CC BY-NC
3609 COMMENT: 3610 COMMENT:
3610 COMPOUND_NAME: Rotenone
3611 RETENTION_TIME: 7.674882 3611 RETENTION_TIME: 7.674882
3612 PRECURSOR_MZ: 395.1498 3612 PRECURSOR_MZ: 395.1498
3613 ADDUCT: [M+H]+ 3613 ADDUCT: [M+H]+
3614 COLLISION_ENERGY: 3614 COLLISION_ENERGY:
3615 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3615 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3616 NUM PEAKS: 118 3616 NUM PEAKS: 118
3617 91.05441 20240.0 3617 91.05441 20240.0
3618 94.04169 8976.0 3618 94.04169 8976.0
3619 95.04953 15733.0 3619 95.04953 15733.0
3620 96.05724 5644.0 3620 96.05724 5644.0
3621 103.05439 9409.0 3621 103.05439 9409.0
3622 105.04505 12948.0 3622 105.04505 12948.0
3623 105.0702 18947.0 3623 105.0702 18947.0
3624 107.04936 14407.0 3624 107.04936 14407.0
3625 108.05726 28276.0 3625 108.05726 28276.0
3626 109.0651 27746.0 3626 109.0651 27746.0
3627 115.05464 7748.0 3627 115.05464 7748.0
3628 118.04178 6690.0 3628 118.04178 6690.0
3629 119.04944 11358.0 3629 119.04944 11358.0
3630 119.0857 16350.0 3630 119.0857 16350.0
3631 121.06523 31422.0 3631 121.06523 31422.0
3632 122.03665 11422.0 3632 122.03665 11422.0
3633 123.04434 5563.0 3633 123.04434 5563.0
3634 124.05232 66924.0 3634 124.05232 66924.0
3635 125.05998 10770.0 3635 125.05998 10770.0
3636 128.06239 12472.0 3636 128.06239 12472.0
3637 129.07021 21798.0 3637 129.07021 21798.0
3638 131.04935 9618.0 3638 131.04935 9618.0
3639 132.05725 6374.0 3639 132.05725 6374.0
3640 133.02864 9569.0 3640 133.02864 9569.0
3641 133.06488 59218.0 3641 133.06488 59218.0
3642 135.04427 48791.0 3642 135.04427 48791.0
3643 135.08092 12734.0 3643 135.08092 12734.0
3644 136.05228 31669.0 3644 136.05228 31669.0
3645 137.05997 22461.0 3645 137.05997 22461.0
3646 139.07579 190263.0 3646 139.07579 190263.0
3647 141.07028 6275.0 3647 141.07028 6275.0
3648 142.07797 14608.0 3648 142.07797 14608.0
3649 143.08594 13615.0 3649 143.08594 13615.0
3650 144.05733 5067.0 3650 144.05733 5067.0
3651 145.0649 8486.0 3651 145.0649 8486.0
3652 147.04451 61525.0 3652 147.04451 61525.0
3653 147.08089 94625.0 3653 147.08089 94625.0
3654 148.0522 39063.0 3654 148.0522 39063.0
3655 149.02341 19610.0 3655 149.02341 19610.0
3656 149.06003 21143.0 3656 149.06003 21143.0
3657 150.06783 16274.0 3657 150.06783 16274.0
3658 151.03905 10391.0 3658 151.03905 10391.0
3659 151.07541 203001.0 3659 151.07541 203001.0
3660 152.04688 7942.0 3660 152.04688 7942.0
3661 152.06248 13044.0 3661 152.06248 13044.0
3662 153.05467 9160.0 3662 153.05467 9160.0
3663 155.0705 50109.0 3663 155.0705 50109.0
3664 155.08604 5247.0 3664 155.08604 5247.0
3665 157.06509 11481.0 3665 157.06509 11481.0
3666 157.10156 7250.0 3666 157.10156 7250.0
3667 159.0446 58047.0 3667 159.0446 58047.0
3668 160.05222 12860.0 3668 160.05222 12860.0
3669 161.02338 80194.0 3669 161.02338 80194.0
3670 161.0601 108267.0 3670 161.0601 108267.0
3671 161.09631 10911.0 3671 161.09631 10911.0
3672 162.0676 99660.0 3672 162.0676 99660.0
3673 163.03929 24087.0 3673 163.03929 24087.0
3674 163.07561 12092.0 3674 163.07561 12092.0
3675 164.04738 8000.0 3675 164.04738 8000.0
3676 165.05518 11042.0 3676 165.05518 11042.0
3677 165.06599 31937.0 3677 165.06599 31937.0
3678 165.09103 67666.0 3678 165.09103 67666.0
3679 167.03391 16070.0 3679 167.03391 16070.0
3680 167.07042 68033.0 3680 167.07042 68033.0
3681 167.08607 14650.0 3681 167.08607 14650.0
3682 169.06497 20549.0 3682 169.06497 20549.0
3683 170.07298 47466.0 3683 170.07298 47466.0
3684 171.0444 8000.0 3684 171.0444 8000.0
3685 171.08104 35499.0 3685 171.08104 35499.0
3686 173.06004 17137.0 3686 173.06004 17137.0
3687 174.06767 6932.0 3687 174.06767 6932.0
3688 175.03938 17059.0 3688 175.03938 17059.0
3689 175.07544 21766.0 3689 175.07544 21766.0
3690 176.04684 21189.0 3690 176.04684 21189.0
3691 177.05479 232262.0 3691 177.05479 232262.0
3692 178.05867 5911.0 3692 178.05867 5911.0
3693 178.0625 25475.0 3693 178.0625 25475.0
3694 179.07047 162479.0 3694 179.07047 162479.0
3695 181.04948 12121.0 3695 181.04948 12121.0
3696 183.08076 4979.0 3696 183.08076 4979.0
3697 185.05991 48654.0 3697 185.05991 48654.0
3698 185.09641 26209.0 3698 185.09641 26209.0
3699 187.03905 10827.0 3699 187.03905 10827.0
3700 188.04747 5292.0 3700 188.04747 5292.0
3701 189.05499 13091.0 3701 189.05499 13091.0
3702 189.09126 53174.0 3702 189.09126 53174.0
3703 191.07039 460509.0 3703 191.07039 460509.0
3704 192.07661 134602.0 3704 192.07661 134602.0
3705 192.07805 420800.0 3705 192.07805 420800.0
3706 193.04977 5384.0 3706 193.04977 5384.0
3707 193.0865 52606.0 3707 193.0865 52606.0
3708 195.08057 343831.0 3708 195.08057 343831.0
3709 197.05963 10859.0 3709 197.05963 10859.0
3710 198.06796 244073.0 3710 198.06796 244073.0
3711 199.07576 11375.0 3711 199.07576 11375.0
3712 201.09085 5454.0 3712 201.09085 5454.0
3713 203.07065 271508.0 3713 203.07065 271508.0
3714 205.0499 11121.0 3714 205.0499 11121.0
3715 211.07547 11767.0 3715 211.07547 11767.0
3716 213.05545 8031.0 3716 213.05545 8031.0
3717 213.09134 496635.0 3717 213.09134 496635.0
3718 219.06538 18652.0 3718 219.06538 18652.0
3719 220.07301 15899.0 3719 220.07301 15899.0
3720 223.07542 20667.0 3720 223.07542 20667.0
3721 226.06303 9493.0 3721 226.06303 9493.0
3722 229.08595 8069.0 3722 229.08595 8069.0
3723 241.08595 34858.0 3723 241.08595 34858.0
3724 309.07611 9652.0 3724 309.07611 9652.0
3725 319.09708 7916.0 3725 319.09708 7916.0
3726 321.11215 19786.0 3726 321.11215 19786.0
3727 331.09756 10399.0 3727 331.09756 10399.0
3728 333.11328 6140.0 3728 333.11328 6140.0
3729 334.08463 6723.0 3729 334.08463 6723.0
3730 335.12769 6532.0 3730 335.12769 6532.0
3731 337.1073 11225.0 3731 337.1073 11225.0
3732 347.091 7782.0 3732 347.091 7782.0
3733 349.10764 9303.0 3733 349.10764 9303.0
3734 377.13797 5836.0 3734 377.13797 5836.0
3735 3735
3736 COMPOUND_NAME: Secbumeton_1
3736 SCANNUMBER: 2214 3737 SCANNUMBER: 2214
3737 IONMODE: Positive 3738 IONMODE: Positive
3738 SPECTRUMTYPE: Centroid 3739 SPECTRUMTYPE: Centroid
3739 FORMULA: C10H19N5O 3740 FORMULA: C10H19N5O
3740 INCHIKEY: ZJMZZNVGNSWOOM-ZETCQYMHSA-N 3741 INCHIKEY: ZJMZZNVGNSWOOM-ZETCQYMHSA-N
3743 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3744 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3744 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3745 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3745 IONIZATION: ESI+ 3746 IONIZATION: ESI+
3746 LICENSE: CC BY-NC 3747 LICENSE: CC BY-NC
3747 COMMENT: 3748 COMMENT:
3748 COMPOUND_NAME: Secbumeton_1
3749 RETENTION_TIME: 3.185351 3749 RETENTION_TIME: 3.185351
3750 PRECURSOR_MZ: 226.1667 3750 PRECURSOR_MZ: 226.1667
3751 ADDUCT: [M+H]+ 3751 ADDUCT: [M+H]+
3752 COLLISION_ENERGY: 3752 COLLISION_ENERGY:
3753 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3753 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3754 NUM PEAKS: 16 3754 NUM PEAKS: 16
3755 85.05116 254026.0 3755 85.05116 254026.0
3756 85.07622 1248785.0 3756 85.07622 1248785.0
3757 86.03511 7693232.0 3757 86.03511 7693232.0
3758 96.05572 2045746.0 3758 96.05572 2045746.0
3759 97.03974 2776563.0 3759 97.03974 2776563.0
3760 99.06665 1175450.0 3760 99.06665 1175450.0
3761 100.05066 9824308.0 3761 100.05066 9824308.0
3762 110.04619 496522.0 3762 110.04619 496522.0
3763 110.0716 223643.0 3763 110.0716 223643.0
3764 114.06643 4195590.0 3764 114.06643 4195590.0
3765 128.08185 3094754.0 3765 128.08185 3094754.0
3766 138.07761 783556.0 3766 138.07761 783556.0
3767 142.07253 19868644.0 3767 142.07253 19868644.0
3768 168.0881 278497.0 3768 168.0881 278497.0
3769 170.10394 12296676.0 3769 170.10394 12296676.0
3770 184.11964 1858746.0 3770 184.11964 1858746.0
3771 3771
3772 COMPOUND_NAME: Secbumeton_2
3772 SCANNUMBER: 2376 3773 SCANNUMBER: 2376
3773 IONMODE: Positive 3774 IONMODE: Positive
3774 SPECTRUMTYPE: Centroid 3775 SPECTRUMTYPE: Centroid
3775 FORMULA: C10H19N5O 3776 FORMULA: C10H19N5O
3776 INCHIKEY: ZJMZZNVGNSWOOM-ZETCQYMHSA-N 3777 INCHIKEY: ZJMZZNVGNSWOOM-ZETCQYMHSA-N
3779 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3780 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3780 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3781 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3781 IONIZATION: ESI+ 3782 IONIZATION: ESI+
3782 LICENSE: CC BY-NC 3783 LICENSE: CC BY-NC
3783 COMMENT: 3784 COMMENT:
3784 COMPOUND_NAME: Secbumeton_2
3785 RETENTION_TIME: 3.288845 3785 RETENTION_TIME: 3.288845
3786 PRECURSOR_MZ: 226.1663 3786 PRECURSOR_MZ: 226.1663
3787 ADDUCT: [M+H]+ 3787 ADDUCT: [M+H]+
3788 COLLISION_ENERGY: 3788 COLLISION_ENERGY:
3789 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3789 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3790 NUM PEAKS: 22 3790 NUM PEAKS: 22
3791 85.05116 203704.0 3791 85.05116 203704.0
3792 85.07622 1795800.0 3792 85.07622 1795800.0
3793 86.03511 4360152.0 3793 86.03511 4360152.0
3794 96.05572 3992152.0 3794 96.05572 3992152.0
3795 97.03974 3296917.0 3795 97.03974 3296917.0
3796 99.06665 489124.0 3796 99.06665 489124.0
3797 100.05066 11922340.0 3797 100.05066 11922340.0
3798 110.04619 311190.0 3798 110.04619 311190.0
3799 110.0716 143123.0 3799 110.0716 143123.0
3800 113.0825 152844.0 3800 113.0825 152844.0
3801 114.06643 5615716.0 3801 114.06643 5615716.0
3802 125.0461 170765.0 3802 125.0461 170765.0
3803 127.09787 169642.0 3803 127.09787 169642.0
3804 128.08185 4145137.0 3804 128.08185 4145137.0
3805 129.0112 167032.0 3805 129.0112 167032.0
3806 138.07761 953215.0 3806 138.07761 953215.0
3807 142.07253 8482599.0 3807 142.07253 8482599.0
3808 153.07755 208846.0 3808 153.07755 208846.0
3809 168.0881 343548.0 3809 168.0881 343548.0
3810 170.10394 12923365.0 3810 170.10394 12923365.0
3811 184.11964 137608.0 3811 184.11964 137608.0
3812 226.16615 243943.0 3812 226.16615 243943.0
3813 3813
3814 COMPOUND_NAME: Spiroxamine_1
3814 SCANNUMBER: 3100 3815 SCANNUMBER: 3100
3815 IONMODE: Positive 3816 IONMODE: Positive
3816 SPECTRUMTYPE: Centroid 3817 SPECTRUMTYPE: Centroid
3817 FORMULA: C18H35NO2 3818 FORMULA: C18H35NO2
3818 INCHIKEY: PUYXTUJWRLOUCW-PQUAAJSLSA-N 3819 INCHIKEY: PUYXTUJWRLOUCW-PQUAAJSLSA-N
3821 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3822 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3822 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3823 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3823 IONIZATION: ESI+ 3824 IONIZATION: ESI+
3824 LICENSE: CC BY-NC 3825 LICENSE: CC BY-NC
3825 COMMENT: 3826 COMMENT:
3826 COMPOUND_NAME: Spiroxamine_1
3827 RETENTION_TIME: 4.508498 3827 RETENTION_TIME: 4.508498
3828 PRECURSOR_MZ: 298.2746 3828 PRECURSOR_MZ: 298.2746
3829 ADDUCT: [M+H]+ 3829 ADDUCT: [M+H]+
3830 COLLISION_ENERGY: 3830 COLLISION_ENERGY:
3831 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3831 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3832 NUM PEAKS: 4 3832 NUM PEAKS: 4
3833 100.11219 3396827.0 3833 100.11219 3396827.0
3834 102.09142 137060.0 3834 102.09142 137060.0
3835 126.12786 85740.0 3835 126.12786 85740.0
3836 144.13857 3215019.0 3836 144.13857 3215019.0
3837 3837
3838 COMPOUND_NAME: Acibenzolar-S-methyl
3838 SCANNUMBER: 6504 3839 SCANNUMBER: 6504
3839 IONMODE: Positive 3840 IONMODE: Positive
3840 SPECTRUMTYPE: Centroid 3841 SPECTRUMTYPE: Centroid
3841 FORMULA: C8H6N2OS2 3842 FORMULA: C8H6N2OS2
3842 INCHIKEY: UELITFHSCLAHKR-UHFFFAOYSA-N 3843 INCHIKEY: UELITFHSCLAHKR-UHFFFAOYSA-N
3845 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3846 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3846 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3847 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3847 IONIZATION: ESI+ 3848 IONIZATION: ESI+
3848 LICENSE: CC BY-NC 3849 LICENSE: CC BY-NC
3849 COMMENT: 3850 COMMENT:
3850 COMPOUND_NAME: Acibenzolar-S-methyl
3851 RETENTION_TIME: 7.209623 3851 RETENTION_TIME: 7.209623
3852 PRECURSOR_MZ: 210.9997 3852 PRECURSOR_MZ: 210.9997
3853 ADDUCT: [M+H]+ 3853 ADDUCT: [M+H]+
3854 COLLISION_ENERGY: 3854 COLLISION_ENERGY:
3855 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3855 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3856 NUM PEAKS: 19 3856 NUM PEAKS: 19
3857 90.96726 85952.0 3857 90.96726 85952.0
3858 91.05441 657143.0 3858 91.05441 657143.0
3859 95.04928 118440.0 3859 95.04928 118440.0
3860 96.00319 401311.0 3860 96.00319 401311.0
3861 104.02592 176500.0 3861 104.02592 176500.0
3862 105.04505 89136.0 3862 105.04505 89136.0
3863 106.99528 418903.0 3863 106.99528 418903.0
3864 108.00302 780675.0 3864 108.00302 780675.0
3865 109.0107 470651.0 3865 109.0107 470651.0
3866 111.02646 108320.0 3866 111.02646 108320.0
3867 121.01091 958564.0 3867 121.01091 958564.0
3868 122.01855 285730.0 3868 122.01855 285730.0
3869 134.99037 663158.0 3869 134.99037 663158.0
3870 135.99904 120240.0 3870 135.99904 120240.0
3871 136.00926 5947453.0 3871 136.00926 5947453.0
3872 139.97499 2000969.0 3872 139.97499 2000969.0
3873 152.98305 216362.0 3873 152.98305 216362.0
3874 167.97003 464522.0 3874 167.97003 464522.0
3875 210.99977 327401.0 3875 210.99977 327401.0
3876 3876
3877 COMPOUND_NAME: Bupirimate
3877 SCANNUMBER: 3267 3878 SCANNUMBER: 3267
3878 IONMODE: Positive 3879 IONMODE: Positive
3879 SPECTRUMTYPE: Centroid 3880 SPECTRUMTYPE: Centroid
3880 FORMULA: C13H24N4O3S 3881 FORMULA: C13H24N4O3S
3881 INCHIKEY: DSKJPMWIHSOYEA-UHFFFAOYSA-N 3882 INCHIKEY: DSKJPMWIHSOYEA-UHFFFAOYSA-N
3884 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3885 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3885 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3886 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3886 IONIZATION: ESI+ 3887 IONIZATION: ESI+
3887 LICENSE: CC BY-NC 3888 LICENSE: CC BY-NC
3888 COMMENT: 3889 COMMENT:
3889 COMPOUND_NAME: Bupirimate
3890 RETENTION_TIME: 6.076324 3890 RETENTION_TIME: 6.076324
3891 PRECURSOR_MZ: 317.1649 3891 PRECURSOR_MZ: 317.1649
3892 ADDUCT: [M+H]+ 3892 ADDUCT: [M+H]+
3893 COLLISION_ENERGY: 3893 COLLISION_ENERGY:
3894 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3894 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3895 NUM PEAKS: 55 3895 NUM PEAKS: 55
3896 86.07153 235598.0 3896 86.07153 235598.0
3897 93.07003 108137.0 3897 93.07003 108137.0
3898 95.06072 255743.0 3898 95.06072 255743.0
3899 95.08585 244503.0 3899 95.08585 244503.0
3900 96.04461 1438629.0 3900 96.04461 1438629.0
3901 96.08099 127976.0 3901 96.08099 127976.0
3902 97.03999 368735.0 3902 97.03999 368735.0
3903 98.06032 1406789.0 3903 98.06032 1406789.0
3904 107.07314 137145.0 3904 107.07314 137145.0
3905 108.01175 7604676.0 3905 108.01175 7604676.0
3906 109.0761 227922.0 3906 109.0761 227922.0
3907 110.06014 169356.0 3907 110.06014 169356.0
3908 110.0716 162792.0 3908 110.0716 162792.0
3909 110.09671 354193.0 3909 110.09671 354193.0
3910 120.081 147452.0 3910 120.081 147452.0
3911 122.07138 411681.0 3911 122.07138 411681.0
3912 122.09673 123475.0 3912 122.09673 123475.0
3913 123.05569 195728.0 3913 123.05569 195728.0
3914 123.09197 115035.0 3914 123.09197 115035.0
3915 124.06344 181991.0 3915 124.06344 181991.0
3916 136.0872 149699.0 3916 136.0872 149699.0
3917 137.05867 120788.0 3917 137.05867 120788.0
3918 137.09485 160672.0 3918 137.09485 160672.0
3919 138.06628 1098460.0 3919 138.06628 1098460.0
3920 138.09154 233604.0 3920 138.09154 233604.0
3921 138.10286 398553.0 3921 138.10286 398553.0
3922 139.07446 1057776.0 3922 139.07446 1057776.0
3923 139.12334 148466.0 3923 139.12334 148466.0
3924 140.10709 5071826.0 3924 140.10709 5071826.0
3925 148.08701 244501.0 3925 148.08701 244501.0
3926 150.10286 2737236.0 3926 150.10286 2737236.0
3927 151.07442 131788.0 3927 151.07442 131788.0
3928 151.11079 210989.0 3928 151.11079 210989.0
3929 151.12326 149447.0 3929 151.12326 149447.0
3930 152.08211 600122.0 3930 152.08211 600122.0
3931 164.08234 442472.0 3931 164.08234 442472.0
3932 165.08989 1444691.0 3932 165.08989 1444691.0
3933 165.10242 2298446.0 3933 165.10242 2298446.0
3934 166.09755 10809536.0 3934 166.09755 10809536.0
3935 167.10577 1006139.0 3935 167.10577 1006139.0
3936 179.12965 335810.0 3936 179.12965 335810.0
3937 180.11362 538952.0 3937 180.11362 538952.0
3938 180.14995 435438.0 3938 180.14995 435438.0
3939 182.12912 1149384.0 3939 182.12912 1149384.0
3940 191.11787 124435.0 3940 191.11787 124435.0
3941 192.14951 246681.0 3941 192.14951 246681.0
3942 193.13402 1395706.0 3942 193.13402 1395706.0
3943 194.12903 1925937.0 3943 194.12903 1925937.0
3944 208.14435 1874942.0 3944 208.14435 1874942.0
3945 209.17653 127377.0 3945 209.17653 127377.0
3946 210.15997 6891096.0 3946 210.15997 6891096.0
3947 224.17574 413548.0 3947 224.17574 413548.0
3948 237.20732 1204267.0 3948 237.20732 1204267.0
3949 262.08615 349666.0 3949 262.08615 349666.0
3950 272.10626 143082.0 3950 272.10626 143082.0
3951 3951
3952 COMPOUND_NAME: Buprofezin
3952 SCANNUMBER: 5627 3953 SCANNUMBER: 5627
3953 IONMODE: Positive 3954 IONMODE: Positive
3954 SPECTRUMTYPE: Centroid 3955 SPECTRUMTYPE: Centroid
3955 FORMULA: C16H23N3OS 3956 FORMULA: C16H23N3OS
3956 INCHIKEY: PRLVTUNWOQKEAI-UHFFFAOYSA-N 3957 INCHIKEY: PRLVTUNWOQKEAI-UHFFFAOYSA-N
3959 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3960 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3960 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3961 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3961 IONIZATION: ESI+ 3962 IONIZATION: ESI+
3962 LICENSE: CC BY-NC 3963 LICENSE: CC BY-NC
3963 COMMENT: 3964 COMMENT:
3964 COMPOUND_NAME: Buprofezin
3965 RETENTION_TIME: 7.028851 3965 RETENTION_TIME: 7.028851
3966 PRECURSOR_MZ: 306.1638 3966 PRECURSOR_MZ: 306.1638
3967 ADDUCT: [M+H]+ 3967 ADDUCT: [M+H]+
3968 COLLISION_ENERGY: 3968 COLLISION_ENERGY:
3969 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3969 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3970 NUM PEAKS: 7 3970 NUM PEAKS: 7
3971 86.06017 3955916.0 3971 86.06017 3955916.0
3972 95.04928 722739.0 3972 95.04928 722739.0
3973 102.03746 765607.0 3973 102.03746 765607.0
3974 102.99629 1020337.0 3974 102.99629 1020337.0
3975 106.06516 49438552.0 3975 106.06516 49438552.0
3976 145.04333 786651.0 3976 145.04333 786651.0
3977 208.05412 1036458.0 3977 208.05412 1036458.0
3978 3978
3979 COMPOUND_NAME: Carboxin
3979 SCANNUMBER: 2650 3980 SCANNUMBER: 2650
3980 IONMODE: Positive 3981 IONMODE: Positive
3981 SPECTRUMTYPE: Centroid 3982 SPECTRUMTYPE: Centroid
3982 FORMULA: C12H13NO2S 3983 FORMULA: C12H13NO2S
3983 INCHIKEY: GYSSRZJIHXQEHQ-UHFFFAOYSA-N 3984 INCHIKEY: GYSSRZJIHXQEHQ-UHFFFAOYSA-N
3986 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 3987 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
3987 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 3988 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
3988 IONIZATION: ESI+ 3989 IONIZATION: ESI+
3989 LICENSE: CC BY-NC 3990 LICENSE: CC BY-NC
3990 COMMENT: 3991 COMMENT:
3991 COMPOUND_NAME: Carboxin
3992 RETENTION_TIME: 5.514598 3992 RETENTION_TIME: 5.514598
3993 PRECURSOR_MZ: 236.0745 3993 PRECURSOR_MZ: 236.0745
3994 ADDUCT: [M+H]+ 3994 ADDUCT: [M+H]+
3995 COLLISION_ENERGY: 3995 COLLISION_ENERGY:
3996 INSTRUMENT_TYPE: LC-ESI-Orbitrap 3996 INSTRUMENT_TYPE: LC-ESI-Orbitrap
3997 NUM PEAKS: 21 3997 NUM PEAKS: 21
3998 86.99005 83162.0 3998 86.99005 83162.0
3999 89.00569 35962.0 3999 89.00569 35962.0
4000 92.0498 113299.0 4000 92.0498 113299.0
4001 93.0575 2928372.0 4001 93.0575 2928372.0
4002 94.06519 52720.0 4002 94.06519 52720.0
4003 95.04928 67153.0 4003 95.04928 67153.0
4004 99.02643 59993.0 4004 99.02643 59993.0
4005 104.04956 151593.0 4005 104.04956 151593.0
4006 105.04476 45581.0 4006 105.04476 45581.0
4007 115.02152 31967.0 4007 115.02152 31967.0
4008 120.04463 57401.0 4008 120.04463 57401.0
4009 124.02155 960327.0 4009 124.02155 960327.0
4010 128.04956 63924.0 4010 128.04956 63924.0
4011 132.04463 580531.0 4011 132.04463 580531.0
4012 138.03711 35055.0 4012 138.03711 35055.0
4013 143.01614 2499380.0 4013 143.01614 2499380.0
4014 146.06033 163428.0 4014 146.06033 163428.0
4015 148.02174 69210.0 4015 148.02174 69210.0
4016 162.03714 126130.0 4016 162.03714 126130.0
4017 165.02444 140508.0 4017 165.02444 140508.0
4018 166.03207 97516.0 4018 166.03207 97516.0
4019 4019
4020 COMPOUND_NAME: Clethodim_1
4020 SCANNUMBER: 4128 4021 SCANNUMBER: 4128
4021 IONMODE: Positive 4022 IONMODE: Positive
4022 SPECTRUMTYPE: Centroid 4023 SPECTRUMTYPE: Centroid
4023 FORMULA: C17H26NO3ClS 4024 FORMULA: C17H26NO3ClS
4024 INCHIKEY: SILSDTWXNBZOGF-KUZBFYBWSA-N 4025 INCHIKEY: SILSDTWXNBZOGF-KUZBFYBWSA-N
4027 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4028 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4028 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4029 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4029 IONIZATION: ESI+ 4030 IONIZATION: ESI+
4030 LICENSE: CC BY-NC 4031 LICENSE: CC BY-NC
4031 COMMENT: 4032 COMMENT:
4032 COMPOUND_NAME: Clethodim_1
4033 RETENTION_TIME: 6.687163 4033 RETENTION_TIME: 6.687163
4034 PRECURSOR_MZ: 360.1401 4034 PRECURSOR_MZ: 360.1401
4035 ADDUCT: [M+H]+ 4035 ADDUCT: [M+H]+
4036 COLLISION_ENERGY: 4036 COLLISION_ENERGY:
4037 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4037 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4038 NUM PEAKS: 93 4038 NUM PEAKS: 93
4039 89.0422 26517.0 4039 89.0422 26517.0
4040 91.05441 49957.0 4040 91.05441 49957.0
4041 92.04956 6055.0 4041 92.04956 6055.0
4042 93.0575 11783.0 4042 93.0575 11783.0
4043 93.07003 33788.0 4043 93.07003 33788.0
4044 94.06519 21009.0 4044 94.06519 21009.0
4045 95.04928 65958.0 4045 95.04928 65958.0
4046 95.0856 11343.0 4046 95.0856 11343.0
4047 96.04461 77264.0 4047 96.04461 77264.0
4048 98.06032 83926.0 4048 98.06032 83926.0
4049 103.05439 27407.0 4049 103.05439 27407.0
4050 105.04505 6981.0 4050 105.04505 6981.0
4051 105.07019 30263.0 4051 105.07019 30263.0
4052 106.06516 86354.0 4052 106.06516 86354.0
4053 107.04936 34964.0 4053 107.04936 34964.0
4054 107.08563 8621.0 4054 107.08563 8621.0
4055 108.0446 28107.0 4055 108.0446 28107.0
4056 108.08108 167346.0 4056 108.08108 167346.0
4057 109.0651 32723.0 4057 109.0651 32723.0
4058 110.06014 31720.0 4058 110.06014 31720.0
4059 110.09671 12453.0 4059 110.09671 12453.0
4060 111.04435 12775.0 4060 111.04435 12775.0
4061 111.06791 6651.0 4061 111.06791 6651.0
4062 114.05498 7671.0 4062 114.05498 7671.0
4063 114.0916 11353.0 4063 114.0916 11353.0
4064 115.0543 6778.0 4064 115.0543 6778.0
4065 117.05739 8001.0 4065 117.05739 8001.0
4066 117.06997 20495.0 4066 117.06997 20495.0
4067 118.06519 20951.0 4067 118.06519 20951.0
4068 119.04944 18911.0 4068 119.04944 18911.0
4069 119.06059 9053.0 4069 119.06059 9053.0
4070 119.0857 23128.0 4070 119.0857 23128.0
4071 120.04463 7579.0 4071 120.04463 7579.0
4072 120.081 8457.0 4072 120.081 8457.0
4073 121.06487 56724.0 4073 121.06487 56724.0
4074 122.06016 65198.0 4074 122.06016 65198.0
4075 122.09673 13384.0 4075 122.09673 13384.0
4076 123.04433 7289.0 4076 123.04433 7289.0
4077 124.03934 5264.0 4077 124.03934 5264.0
4078 124.07605 20748.0 4078 124.07605 20748.0
4079 127.02138 23658.0 4079 127.02138 23658.0
4080 128.06201 5671.0 4080 128.06201 5671.0
4081 129.07021 5839.0 4081 129.07021 5839.0
4082 131.0731 6698.0 4082 131.0731 6698.0
4083 131.08559 5362.0 4083 131.08559 5362.0
4084 132.08089 18560.0 4084 132.08089 18560.0
4085 133.06488 10377.0 4085 133.06488 10377.0
4086 133.10155 8105.0 4086 133.10155 8105.0
4087 134.06033 147188.0 4087 134.06033 147188.0
4088 134.09659 13221.0 4088 134.09659 13221.0
4089 135.08049 8346.0 4089 135.08049 8346.0
4090 136.03949 70010.0 4090 136.03949 70010.0
4091 136.07568 371565.0 4091 136.07568 371565.0
4092 136.11234 9112.0 4092 136.11234 9112.0
4093 137.05997 23108.0 4093 137.05997 23108.0
4094 138.05496 9422.0 4094 138.05496 9422.0
4095 138.09154 20890.0 4095 138.09154 20890.0
4096 144.08099 5145.0 4096 144.08099 5145.0
4097 145.0649 6292.0 4097 145.0649 6292.0
4098 146.06033 26112.0 4098 146.06033 26112.0
4099 146.09634 7672.0 4099 146.09634 7672.0
4100 147.04402 77322.0 4100 147.04402 77322.0
4101 147.08089 12959.0 4101 147.08089 12959.0
4102 148.0759 20412.0 4102 148.0759 20412.0
4103 149.04733 5916.0 4103 149.04733 5916.0
4104 149.06003 102646.0 4104 149.06003 102646.0
4105 150.05499 6525.0 4105 150.05499 6525.0
4106 150.09151 15556.0 4106 150.09151 15556.0
4107 150.12804 6161.0 4107 150.12804 6161.0
4108 152.07053 18217.0 4108 152.07053 18217.0
4109 158.04488 6800.0 4109 158.04488 6800.0
4110 160.07613 16467.0 4110 160.07613 16467.0
4111 160.11201 5212.0 4111 160.11201 5212.0
4112 161.0601 8950.0 4112 161.0601 8950.0
4113 161.09631 9597.0 4113 161.09631 9597.0
4114 162.0554 6952.0 4114 162.0554 6952.0
4115 162.0914 19731.0 4115 162.0914 19731.0
4116 163.06274 15231.0 4116 163.06274 15231.0
4117 164.07106 350022.0 4117 164.07106 350022.0
4118 164.10716 16374.0 4118 164.10716 16374.0
4119 166.08664 512799.0 4119 166.08664 512799.0
4120 166.12283 13211.0 4120 166.12283 13211.0
4121 167.09418 26398.0 4121 167.09418 26398.0
4122 173.50754 5344.0 4122 173.50754 5344.0
4123 178.08673 16500.0 4123 178.08673 16500.0
4124 178.12309 12987.0 4124 178.12309 12987.0
4125 180.08443 5978.0 4125 180.08443 5978.0
4126 180.10194 6844.0 4126 180.10194 6844.0
4127 190.1227 6425.0 4127 190.1227 6425.0
4128 192.10233 16067.0 4128 192.10233 16067.0
4129 206.11787 6696.0 4129 206.11787 6696.0
4130 212.11047 16431.0 4130 212.11047 16431.0
4131 240.10542 8682.0 4131 240.10542 8682.0
4132 4132
4133 COMPOUND_NAME: Clethodim_2
4133 SCANNUMBER: 7016 4134 SCANNUMBER: 7016
4134 IONMODE: Positive 4135 IONMODE: Positive
4135 SPECTRUMTYPE: Centroid 4136 SPECTRUMTYPE: Centroid
4136 FORMULA: C17H26NO3ClS 4137 FORMULA: C17H26NO3ClS
4137 INCHIKEY: SILSDTWXNBZOGF-KUZBFYBWSA-N 4138 INCHIKEY: SILSDTWXNBZOGF-KUZBFYBWSA-N
4140 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4141 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4141 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4142 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4142 IONIZATION: ESI+ 4143 IONIZATION: ESI+
4143 LICENSE: CC BY-NC 4144 LICENSE: CC BY-NC
4144 COMMENT: 4145 COMMENT:
4145 COMPOUND_NAME: Clethodim_2
4146 RETENTION_TIME: 7.277172 4146 RETENTION_TIME: 7.277172
4147 PRECURSOR_MZ: 360.1401 4147 PRECURSOR_MZ: 360.1401
4148 ADDUCT: [M+H]+ 4148 ADDUCT: [M+H]+
4149 COLLISION_ENERGY: 4149 COLLISION_ENERGY:
4150 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4150 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4151 NUM PEAKS: 68 4151 NUM PEAKS: 68
4152 89.0422 98238.0 4152 89.0422 98238.0
4153 91.05464 171745.0 4153 91.05464 171745.0
4154 93.05774 38046.0 4154 93.05774 38046.0
4155 93.07027 136004.0 4155 93.07027 136004.0
4156 94.06543 101832.0 4156 94.06543 101832.0
4157 95.04953 227900.0 4157 95.04953 227900.0
4158 95.08585 40869.0 4158 95.08585 40869.0
4159 96.04461 221541.0 4159 96.04461 221541.0
4160 98.06032 529705.0 4160 98.06032 529705.0
4161 103.05467 131256.0 4161 103.05467 131256.0
4162 105.07019 127685.0 4162 105.07019 127685.0
4163 106.06545 53082.0 4163 106.06545 53082.0
4164 107.04936 136788.0 4164 107.04936 136788.0
4165 107.08593 34588.0 4165 107.08593 34588.0
4166 108.0446 65341.0 4166 108.0446 65341.0
4167 108.08108 867554.0 4167 108.08108 867554.0
4168 109.0651 107578.0 4168 109.0651 107578.0
4169 110.06044 125419.0 4169 110.06044 125419.0
4170 111.04435 54097.0 4170 111.04435 54097.0
4171 111.06822 33474.0 4171 111.06822 33474.0
4172 114.0916 70953.0 4172 114.0916 70953.0
4173 117.07031 92684.0 4173 117.07031 92684.0
4174 118.06553 57896.0 4174 118.06553 57896.0
4175 119.04944 77592.0 4175 119.04944 77592.0
4176 119.0857 101869.0 4176 119.0857 101869.0
4177 120.081 44118.0 4177 120.081 44118.0
4178 121.06523 314215.0 4178 121.06523 314215.0
4179 122.06016 283363.0 4179 122.06016 283363.0
4180 122.09673 58647.0 4180 122.09673 58647.0
4181 124.07605 110151.0 4181 124.07605 110151.0
4182 127.02138 108658.0 4182 127.02138 108658.0
4183 133.10155 43604.0 4183 133.10155 43604.0
4184 134.06033 82368.0 4184 134.06033 82368.0
4185 134.09659 80374.0 4185 134.09659 80374.0
4186 135.08092 42793.0 4186 135.08092 42793.0
4187 136.07613 1946515.0 4187 136.07613 1946515.0
4188 136.11234 44348.0 4188 136.11234 44348.0
4189 137.05997 112159.0 4189 137.05997 112159.0
4190 138.05539 37327.0 4190 138.05539 37327.0
4191 138.09154 107538.0 4191 138.09154 107538.0
4192 146.06033 140672.0 4192 146.06033 140672.0
4193 146.09682 35123.0 4193 146.09682 35123.0
4194 147.04449 448482.0 4194 147.04449 448482.0
4195 147.06795 32058.0 4195 147.06795 32058.0
4196 147.08089 54066.0 4196 147.08089 54066.0
4197 148.0759 90038.0 4197 148.0759 90038.0
4198 149.06003 660024.0 4198 149.06003 660024.0
4199 150.09151 33706.0 4199 150.09151 33706.0
4200 152.07103 119001.0 4200 152.07103 119001.0
4201 161.0601 46725.0 4201 161.0601 46725.0
4202 161.09631 40686.0 4202 161.09631 40686.0
4203 162.09196 88271.0 4203 162.09196 88271.0
4204 163.06331 31458.0 4204 163.06331 31458.0
4205 164.07106 2144695.0 4205 164.07106 2144695.0
4206 164.10716 97593.0 4206 164.10716 97593.0
4207 166.08664 3133889.0 4207 166.08664 3133889.0
4208 166.12283 98337.0 4208 166.12283 98337.0
4209 167.09418 133413.0 4209 167.09418 133413.0
4210 177.07883 31343.0 4210 177.07883 31343.0
4211 178.12309 80524.0 4211 178.12309 80524.0
4212 179.09425 38320.0 4212 179.09425 38320.0
4213 180.10194 39682.0 4213 180.10194 39682.0
4214 190.1227 42958.0 4214 190.1227 42958.0
4215 192.10233 115116.0 4215 192.10233 115116.0
4216 206.11787 45529.0 4216 206.11787 45529.0
4217 208.13387 37258.0 4217 208.13387 37258.0
4218 212.11047 103531.0 4218 212.11047 103531.0
4219 240.10542 87328.0 4219 240.10542 87328.0
4220 4220
4221 COMPOUND_NAME: Clothianidin
4221 SCANNUMBER: 1358 4222 SCANNUMBER: 1358
4222 IONMODE: Positive 4223 IONMODE: Positive
4223 SPECTRUMTYPE: Centroid 4224 SPECTRUMTYPE: Centroid
4224 FORMULA: C6H8N5O2ClS 4225 FORMULA: C6H8N5O2ClS
4225 INCHIKEY: PGOOBECODWQEAB-UHFFFAOYSA-N 4226 INCHIKEY: PGOOBECODWQEAB-UHFFFAOYSA-N
4228 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4229 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4229 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4230 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4230 IONIZATION: ESI+ 4231 IONIZATION: ESI+
4231 LICENSE: CC BY-NC 4232 LICENSE: CC BY-NC
4232 COMMENT: 4233 COMMENT:
4233 COMPOUND_NAME: Clothianidin
4234 RETENTION_TIME: 2.767634 4234 RETENTION_TIME: 2.767634
4235 PRECURSOR_MZ: 250.0162 4235 PRECURSOR_MZ: 250.0162
4236 ADDUCT: [M+H]+ 4236 ADDUCT: [M+H]+
4237 COLLISION_ENERGY: 4237 COLLISION_ENERGY:
4238 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4238 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4239 NUM PEAKS: 12 4239 NUM PEAKS: 12
4240 113.01702 68898.0 4240 113.01702 68898.0
4241 131.96729 1556136.0 4241 131.96729 1556136.0
4242 146.97801 24619.0 4242 146.97801 24619.0
4243 168.04659 701063.0 4243 168.04659 701063.0
4244 169.05435 2394222.0 4244 169.05435 2394222.0
4245 172.98125 33776.0 4245 172.98125 33776.0
4246 174.9729 46060.0 4246 174.9729 46060.0
4247 203.01552 30320.0 4247 203.01552 30320.0
4248 204.02304 121736.0 4248 204.02304 121736.0
4249 206.01546 199604.0 4249 206.01546 199604.0
4250 220.01871 34828.0 4250 220.01871 34828.0
4251 250.01668 782407.0 4251 250.01668 782407.0
4252 4252
4253 COMPOUND_NAME: Cyazofamid
4253 SCANNUMBER: 4651 4254 SCANNUMBER: 4651
4254 IONMODE: Positive 4255 IONMODE: Positive
4255 SPECTRUMTYPE: Centroid 4256 SPECTRUMTYPE: Centroid
4256 FORMULA: C13H13N4O2ClS 4257 FORMULA: C13H13N4O2ClS
4257 INCHIKEY: YXKMMRDKEKCERS-UHFFFAOYSA-N 4258 INCHIKEY: YXKMMRDKEKCERS-UHFFFAOYSA-N
4260 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4261 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4261 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4262 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4262 IONIZATION: ESI+ 4263 IONIZATION: ESI+
4263 LICENSE: CC BY-NC 4264 LICENSE: CC BY-NC
4264 COMMENT: 4265 COMMENT:
4265 COMPOUND_NAME: Cyazofamid
4266 RETENTION_TIME: 6.824718 4266 RETENTION_TIME: 6.824718
4267 PRECURSOR_MZ: 325.0526 4267 PRECURSOR_MZ: 325.0526
4268 ADDUCT: [M+H]+ 4268 ADDUCT: [M+H]+
4269 COLLISION_ENERGY: 4269 COLLISION_ENERGY:
4270 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4270 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4271 NUM PEAKS: 14 4271 NUM PEAKS: 14
4272 108.01175 7160721.0 4272 108.01175 7160721.0
4273 216.03249 215458.0 4273 216.03249 215458.0
4274 217.0407 634975.0 4274 217.0407 634975.0
4275 218.0482 106134.0 4275 218.0482 106134.0
4276 225.11369 156877.0 4276 225.11369 156877.0
4277 226.12143 91884.0 4277 226.12143 91884.0
4278 233.06017 429313.0 4278 233.06017 429313.0
4279 251.07034 448093.0 4279 251.07034 448093.0
4280 251.10664 310661.0 4280 251.10664 310661.0
4281 261.09036 1553497.0 4281 261.09036 1553497.0
4282 279.10236 522333.0 4282 279.10236 522333.0
4283 325.052 1817226.0 4283 325.052 1817226.0
4284 325.14325 121241.0 4284 325.14325 121241.0
4285 325.23611 85648.0 4285 325.23611 85648.0
4286 4286
4287 COMPOUND_NAME: Ethiprole
4287 SCANNUMBER: 2873 4288 SCANNUMBER: 2873
4288 IONMODE: Positive 4289 IONMODE: Positive
4289 SPECTRUMTYPE: Centroid 4290 SPECTRUMTYPE: Centroid
4290 FORMULA: C13H9N4OCl2F3S 4291 FORMULA: C13H9N4OCl2F3S
4291 INCHIKEY: FNELVJVBIYMIMC-UHFFFAOYSA-N 4292 INCHIKEY: FNELVJVBIYMIMC-UHFFFAOYSA-N
4294 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4295 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4295 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4296 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4296 IONIZATION: ESI+ 4297 IONIZATION: ESI+
4297 LICENSE: CC BY-NC 4298 LICENSE: CC BY-NC
4298 COMMENT: 4299 COMMENT:
4299 COMPOUND_NAME: Ethiprole
4300 RETENTION_TIME: 5.828761 4300 RETENTION_TIME: 5.828761
4301 PRECURSOR_MZ: 396.991 4301 PRECURSOR_MZ: 396.991
4302 ADDUCT: [M+H]+ 4302 ADDUCT: [M+H]+
4303 COLLISION_ENERGY: 4303 COLLISION_ENERGY:
4304 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4304 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4305 NUM PEAKS: 11 4305 NUM PEAKS: 11
4306 212.94865 522963.0 4306 212.94865 522963.0
4307 227.9595 466048.0 4307 227.9595 466048.0
4308 240.95441 720208.0 4308 240.95441 720208.0
4309 254.9706 13822754.0 4309 254.9706 13822754.0
4310 263.97287 158454.0 4310 263.97287 158454.0
4311 271.93167 238242.0 4311 271.93167 238242.0
4312 288.95517 162603.0 4312 288.95517 162603.0
4313 288.96835 478467.0 4313 288.96835 478467.0
4314 315.97946 548987.0 4314 315.97946 548987.0
4315 323.93817 233169.0 4315 323.93817 233169.0
4316 350.94952 1933706.0 4316 350.94952 1933706.0
4317 4317
4318 COMPOUND_NAME: Ethofumesate
4318 SCANNUMBER: 3176 4319 SCANNUMBER: 3176
4319 IONMODE: Positive 4320 IONMODE: Positive
4320 SPECTRUMTYPE: Centroid 4321 SPECTRUMTYPE: Centroid
4321 FORMULA: C13H18O5S 4322 FORMULA: C13H18O5S
4322 INCHIKEY: IRCMYGHHKLLGHV-GFCCVEGCSA-N 4323 INCHIKEY: IRCMYGHHKLLGHV-GFCCVEGCSA-N
4325 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4326 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4326 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4327 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4327 IONIZATION: ESI+ 4328 IONIZATION: ESI+
4328 LICENSE: CC BY-NC 4329 LICENSE: CC BY-NC
4329 COMMENT: 4330 COMMENT:
4330 COMPOUND_NAME: Ethofumesate
4331 RETENTION_TIME: 6.01901 4331 RETENTION_TIME: 6.01901
4332 PRECURSOR_MZ: 287.0957 4332 PRECURSOR_MZ: 287.0957
4333 ADDUCT: [M+H]+ 4333 ADDUCT: [M+H]+
4334 COLLISION_ENERGY: 4334 COLLISION_ENERGY:
4335 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4335 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4336 NUM PEAKS: 10 4336 NUM PEAKS: 10
4337 121.06523 2086509.0 4337 121.06523 2086509.0
4338 149.09618 158152.0 4338 149.09618 158152.0
4339 161.0601 278315.0 4339 161.0601 278315.0
4340 162.0676 51729.0 4340 162.0676 51729.0
4341 163.07561 321436.0 4341 163.07561 321436.0
4342 179.07047 102226.0 4342 179.07047 102226.0
4343 241.05281 803837.0 4343 241.05281 803837.0
4344 259.06424 3450423.0 4344 259.06424 3450423.0
4345 277.07498 105295.0 4345 277.07498 105295.0
4346 287.09497 1000737.0 4346 287.09497 1000737.0
4347 4347
4348 COMPOUND_NAME: Fenamidone
4348 SCANNUMBER: 4022 4349 SCANNUMBER: 4022
4349 IONMODE: Positive 4350 IONMODE: Positive
4350 SPECTRUMTYPE: Centroid 4351 SPECTRUMTYPE: Centroid
4351 FORMULA: C17H17N3OS 4352 FORMULA: C17H17N3OS
4352 INCHIKEY: LMVPQMGRYSRMIW-KRWDZBQOSA-N 4353 INCHIKEY: LMVPQMGRYSRMIW-KRWDZBQOSA-N
4355 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4356 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4356 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4357 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4357 IONIZATION: ESI+ 4358 IONIZATION: ESI+
4358 LICENSE: CC BY-NC 4359 LICENSE: CC BY-NC
4359 COMMENT: 4360 COMMENT:
4360 COMPOUND_NAME: Fenamidone
4361 RETENTION_TIME: 6.626915 4361 RETENTION_TIME: 6.626915
4362 PRECURSOR_MZ: 312.1172 4362 PRECURSOR_MZ: 312.1172
4363 ADDUCT: [M+H]+ 4363 ADDUCT: [M+H]+
4364 COLLISION_ENERGY: 4364 COLLISION_ENERGY:
4365 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4365 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4366 NUM PEAKS: 23 4366 NUM PEAKS: 23
4367 92.0498 32114948.0 4367 92.0498 32114948.0
4368 103.05439 9639649.0 4368 103.05439 9639649.0
4369 104.04984 654872.0 4369 104.04984 654872.0
4370 118.05279 339058.0 4370 118.05279 339058.0
4371 120.081 4707760.0 4371 120.081 4707760.0
4372 124.07605 564026.0 4372 124.07605 564026.0
4373 133.06364 333596.0 4373 133.06364 333596.0
4374 133.07642 2035568.0 4374 133.07642 2035568.0
4375 134.07159 10042268.0 4375 134.07159 10042268.0
4376 150.02492 4123380.0 4376 150.02492 4123380.0
4377 158.07153 1565433.0 4377 158.07153 1565433.0
4378 161.07108 557286.0 4378 161.07108 557286.0
4379 165.04834 2679578.0 4379 165.04834 2679578.0
4380 170.09679 350930.0 4380 170.09679 350930.0
4381 194.09637 1767185.0 4381 194.09637 1767185.0
4382 195.09152 465030.0 4382 195.09152 465030.0
4383 206.08372 504328.0 4383 206.08372 504328.0
4384 207.06779 429040.0 4384 207.06779 429040.0
4385 211.12321 535099.0 4385 211.12321 535099.0
4386 219.09235 850480.0 4386 219.09235 850480.0
4387 221.0947 1138537.0 4387 221.0947 1138537.0
4388 236.11884 5452674.0 4388 236.11884 5452674.0
4389 237.04855 688489.0 4389 237.04855 688489.0
4390 4390
4391 COMPOUND_NAME: Fipronil
4391 SCANNUMBER: 3428 4392 SCANNUMBER: 3428
4392 IONMODE: Positive 4393 IONMODE: Positive
4393 SPECTRUMTYPE: Centroid 4394 SPECTRUMTYPE: Centroid
4394 FORMULA: C12H4N4OCl2F6S 4395 FORMULA: C12H4N4OCl2F6S
4395 INCHIKEY: ZOCSXAVNDGMNBV-UHFFFAOYSA-N 4396 INCHIKEY: ZOCSXAVNDGMNBV-UHFFFAOYSA-N
4398 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4399 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4399 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4400 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4400 IONIZATION: ESI+ 4401 IONIZATION: ESI+
4401 LICENSE: CC BY-NC 4402 LICENSE: CC BY-NC
4402 COMMENT: 4403 COMMENT:
4403 COMPOUND_NAME: Fipronil
4404 RETENTION_TIME: 6.367518 4404 RETENTION_TIME: 6.367518
4405 PRECURSOR_MZ: 436.9474 4405 PRECURSOR_MZ: 436.9474
4406 ADDUCT: [M+H]+ 4406 ADDUCT: [M+H]+
4407 COLLISION_ENERGY: 4407 COLLISION_ENERGY:
4408 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4408 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4409 NUM PEAKS: 44 4409 NUM PEAKS: 44
4410 85.96982 4313.0 4410 85.96982 4313.0
4411 113.00444 3712.0 4411 113.00444 3712.0
4412 113.98832 5133.0 4412 113.98832 5133.0
4413 139.99144 7362.0 4413 139.99144 7362.0
4414 212.94781 4882.0 4414 212.94781 4882.0
4415 221.00912 225249.0 4415 221.00912 225249.0
4416 227.95949 26131.0 4416 227.95949 26131.0
4417 228.96689 57334.0 4417 228.96689 57334.0
4418 229.97443 5477.0 4418 229.97443 5477.0
4419 238.95135 20431.0 4419 238.95135 20431.0
4420 239.95872 31698.0 4420 239.95872 31698.0
4421 240.95441 5173.0 4421 240.95441 5173.0
4422 246.00426 38514.0 4422 246.00426 38514.0
4423 246.98785 4361.0 4423 246.98785 4361.0
4424 249.00337 20177.0 4424 249.00337 20177.0
4425 252.98164 49955.0 4425 252.98164 49955.0
4426 253.96179 34002.0 4426 253.96179 34002.0
4427 254.96948 369569.0 4427 254.96948 369569.0
4428 255.97771 5120.0 4428 255.97771 5120.0
4429 256.92007 8581.0 4429 256.92007 8581.0
4430 257.96988 6310.0 4430 257.96988 6310.0
4431 258.00436 15884.0 4431 258.00436 15884.0
4432 262.96518 141114.0 4432 262.96518 141114.0
4433 263.94986 4319.0 4433 263.94986 4319.0
4434 264.95398 10810.0 4434 264.95398 10810.0
4435 265.00839 13074.0 4435 265.00839 13074.0
4436 266.97012 5374.0 4436 266.97012 5374.0
4437 270.00439 13928.0 4437 270.00439 13928.0
4438 270.92358 71148.0 4438 270.92358 71148.0
4439 277.9621 52537.0 4439 277.9621 52537.0
4440 280.97632 110429.0 4440 280.97632 110429.0
4441 281.98138 13157.0 4441 281.98138 13157.0
4442 284.00772 9139.0 4442 284.00772 9139.0
4443 285.01489 32296.0 4443 285.01489 32296.0
4444 287.96118 3855.0 4444 287.96118 3855.0
4445 289.97687 181252.0 4445 289.97687 181252.0
4446 305.97165 38958.0 4446 305.97165 38958.0
4447 314.97189 30271.0 4447 314.97189 30271.0
4448 315.97946 17897.0 4448 315.97946 17897.0
4449 319.98468 18911.0 4449 319.98468 18911.0
4450 332.98279 23894.0 4450 332.98279 23894.0
4451 341.94772 7327.0 4451 341.94772 7327.0
4452 350.94775 6206.0 4452 350.94775 6206.0
4453 367.95102 6446.0 4453 367.95102 6446.0
4454 4454
4455 COMPOUND_NAME: Flufenacet
4455 SCANNUMBER: 3663 4456 SCANNUMBER: 3663
4456 IONMODE: Positive 4457 IONMODE: Positive
4457 SPECTRUMTYPE: Centroid 4458 SPECTRUMTYPE: Centroid
4458 FORMULA: C14H13N3O2F4S 4459 FORMULA: C14H13N3O2F4S
4459 INCHIKEY: IANUJLZYFUDJIH-UHFFFAOYSA-N 4460 INCHIKEY: IANUJLZYFUDJIH-UHFFFAOYSA-N
4462 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4463 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4463 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4464 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4464 IONIZATION: ESI+ 4465 IONIZATION: ESI+
4465 LICENSE: CC BY-NC 4466 LICENSE: CC BY-NC
4466 COMMENT: 4467 COMMENT:
4467 COMPOUND_NAME: Flufenacet
4468 RETENTION_TIME: 6.476889 4468 RETENTION_TIME: 6.476889
4469 PRECURSOR_MZ: 364.0744 4469 PRECURSOR_MZ: 364.0744
4470 ADDUCT: [M+H]+ 4470 ADDUCT: [M+H]+
4471 COLLISION_ENERGY: 4471 COLLISION_ENERGY:
4472 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4472 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4473 NUM PEAKS: 5 4473 NUM PEAKS: 5
4474 124.05603 201655.0 4474 124.05603 201655.0
4475 152.0509 5487354.0 4475 152.0509 5487354.0
4476 152.08713 528888.0 4476 152.08713 528888.0
4477 194.09782 19271964.0 4477 194.09782 19271964.0
4478 364.07422 2107439.0 4478 364.07422 2107439.0
4479 4479
4480 COMPOUND_NAME: Hexythiazox
4480 SCANNUMBER: 7986 4481 SCANNUMBER: 7986
4481 IONMODE: Positive 4482 IONMODE: Positive
4482 SPECTRUMTYPE: Centroid 4483 SPECTRUMTYPE: Centroid
4483 FORMULA: C17H21N2O2ClS 4484 FORMULA: C17H21N2O2ClS
4484 INCHIKEY: XGWIJUOSCAQSSV-XHDPSFHLSA-N 4485 INCHIKEY: XGWIJUOSCAQSSV-XHDPSFHLSA-N
4487 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4488 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4488 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4489 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4489 IONIZATION: ESI+ 4490 IONIZATION: ESI+
4490 LICENSE: CC BY-NC 4491 LICENSE: CC BY-NC
4491 COMMENT: 4492 COMMENT:
4492 COMPOUND_NAME: Hexythiazox
4493 RETENTION_TIME: 7.46046 4493 RETENTION_TIME: 7.46046
4494 PRECURSOR_MZ: 353.1096 4494 PRECURSOR_MZ: 353.1096
4495 ADDUCT: [M+H]+ 4495 ADDUCT: [M+H]+
4496 COLLISION_ENERGY: 4496 COLLISION_ENERGY:
4497 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4497 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4498 NUM PEAKS: 18 4498 NUM PEAKS: 18
4499 115.0543 1419536.0 4499 115.0543 1419536.0
4500 116.06212 1728574.0 4500 116.06212 1728574.0
4501 117.05739 141175.0 4501 117.05739 141175.0
4502 125.01533 77703.0 4502 125.01533 77703.0
4503 132.08089 464129.0 4503 132.08089 464129.0
4504 133.06488 142255.0 4504 133.06488 142255.0
4505 133.08878 1059309.0 4505 133.08878 1059309.0
4506 140.04968 116606.0 4506 140.04968 116606.0
4507 141.05769 118308.0 4507 141.05769 118308.0
4508 143.06068 285902.0 4508 143.06068 285902.0
4509 151.03107 3098662.0 4509 151.03107 3098662.0
4510 153.03435 252766.0 4510 153.03435 252766.0
4511 159.06828 444319.0 4511 159.06828 444319.0
4512 168.05769 6763262.0 4512 168.05769 6763262.0
4513 176.02615 779438.0 4513 176.02615 779438.0
4514 194.03688 1165217.0 4514 194.03688 1165217.0
4515 210.01369 101590.0 4515 210.01369 101590.0
4516 228.02509 203533.0 4516 228.02509 203533.0
4517 4517
4518 COMPOUND_NAME: Mefenacet
4518 SCANNUMBER: 6090 4519 SCANNUMBER: 6090
4519 IONMODE: Positive 4520 IONMODE: Positive
4520 SPECTRUMTYPE: Centroid 4521 SPECTRUMTYPE: Centroid
4521 FORMULA: C16H14N2O2S 4522 FORMULA: C16H14N2O2S
4522 INCHIKEY: XIGAUIHYSDTJHW-UHFFFAOYSA-N 4523 INCHIKEY: XIGAUIHYSDTJHW-UHFFFAOYSA-N
4525 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4526 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4526 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4527 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4527 IONIZATION: ESI+ 4528 IONIZATION: ESI+
4528 LICENSE: CC BY-NC 4529 LICENSE: CC BY-NC
4529 COMMENT: 4530 COMMENT:
4530 COMPOUND_NAME: Mefenacet
4531 RETENTION_TIME: 7.143147 4531 RETENTION_TIME: 7.143147
4532 PRECURSOR_MZ: 299.0857 4532 PRECURSOR_MZ: 299.0857
4533 ADDUCT: [M+H]+ 4533 ADDUCT: [M+H]+
4534 COLLISION_ENERGY: 4534 COLLISION_ENERGY:
4535 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4535 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4536 NUM PEAKS: 10 4536 NUM PEAKS: 10
4537 91.05441 4904942.0 4537 91.05441 4904942.0
4538 93.07003 396728.0 4538 93.07003 396728.0
4539 95.04928 309109.0 4539 95.04928 309109.0
4540 103.05439 240325.0 4540 103.05439 240325.0
4541 105.05748 315163.0 4541 105.05748 315163.0
4542 118.06553 748880.0 4542 118.06553 748880.0
4543 120.081 20302168.0 4543 120.081 20302168.0
4544 136.02161 2145909.0 4544 136.02161 2145909.0
4545 148.0759 2833957.0 4545 148.0759 2833957.0
4546 152.01669 272045.0 4546 152.01669 272045.0
4547 4547
4548 COMPOUND_NAME: Mesotrione
4548 SCANNUMBER: 1880 4549 SCANNUMBER: 1880
4549 IONMODE: Positive 4550 IONMODE: Positive
4550 SPECTRUMTYPE: Centroid 4551 SPECTRUMTYPE: Centroid
4551 FORMULA: C14H13NO7S 4552 FORMULA: C14H13NO7S
4552 INCHIKEY: KPUREKXXPHOJQT-UHFFFAOYSA-N 4553 INCHIKEY: KPUREKXXPHOJQT-UHFFFAOYSA-N
4555 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4556 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4556 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4557 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4557 IONIZATION: ESI+ 4558 IONIZATION: ESI+
4558 LICENSE: CC BY-NC 4559 LICENSE: CC BY-NC
4559 COMMENT: 4560 COMMENT:
4560 COMPOUND_NAME: Mesotrione
4561 RETENTION_TIME: 4.438974 4561 RETENTION_TIME: 4.438974
4562 PRECURSOR_MZ: 340.0492 4562 PRECURSOR_MZ: 340.0492
4563 ADDUCT: [M+H]+ 4563 ADDUCT: [M+H]+
4564 COLLISION_ENERGY: 4564 COLLISION_ENERGY:
4565 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4565 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4566 NUM PEAKS: 21 4566 NUM PEAKS: 21
4567 92.0498 20384.0 4567 92.0498 20384.0
4568 94.02896 22521.0 4568 94.02896 22521.0
4569 95.01298 42541.0 4569 95.01298 42541.0
4570 104.01339 1414098.0 4570 104.01339 1414098.0
4571 107.0131 68271.0 4571 107.0131 68271.0
4572 108.02079 22960.0 4572 108.02079 22960.0
4573 111.04435 27776.0 4573 111.04435 27776.0
4574 119.01284 29585.0 4574 119.01284 29585.0
4575 122.02398 38301.0 4575 122.02398 38301.0
4576 136.03949 15704.0 4576 136.03949 15704.0
4577 154.97983 175640.0 4577 154.97983 175640.0
4578 166.0137 179306.0 4578 166.0137 179306.0
4579 170.00336 47194.0 4579 170.00336 47194.0
4580 182.0032 34021.0 4580 182.0032 34021.0
4581 214.06305 78325.0 4581 214.06305 78325.0
4582 216.00862 81842.0 4582 216.00862 81842.0
4583 227.99644 875193.0 4583 227.99644 875193.0
4584 260.02258 25724.0 4584 260.02258 25724.0
4585 275.03772 37760.0 4585 275.03772 37760.0
4586 293.04776 19676.0 4586 293.04776 19676.0
4587 294.05606 18376.0 4587 294.05606 18376.0
4588 4588
4589 COMPOUND_NAME: Methoprotryne
4589 SCANNUMBER: 2365 4590 SCANNUMBER: 2365
4590 IONMODE: Positive 4591 IONMODE: Positive
4591 SPECTRUMTYPE: Centroid 4592 SPECTRUMTYPE: Centroid
4592 FORMULA: C11H21N5OS 4593 FORMULA: C11H21N5OS
4593 INCHIKEY: DDUIUBPJPOKOMV-UHFFFAOYSA-N 4594 INCHIKEY: DDUIUBPJPOKOMV-UHFFFAOYSA-N
4596 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4597 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4597 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4598 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4598 IONIZATION: ESI+ 4599 IONIZATION: ESI+
4599 LICENSE: CC BY-NC 4600 LICENSE: CC BY-NC
4600 COMMENT: 4601 COMMENT:
4601 COMPOUND_NAME: Methoprotryne
4602 RETENTION_TIME: 4.953537 4602 RETENTION_TIME: 4.953537
4603 PRECURSOR_MZ: 272.1545 4603 PRECURSOR_MZ: 272.1545
4604 ADDUCT: [M+H]+ 4604 ADDUCT: [M+H]+
4605 COLLISION_ENERGY: 4605 COLLISION_ENERGY:
4606 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4606 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4607 NUM PEAKS: 15 4607 NUM PEAKS: 15
4608 91.03273 1224280.0 4608 91.03273 1224280.0
4609 103.03277 469421.0 4609 103.03277 469421.0
4610 108.05575 1098439.0 4610 108.05575 1098439.0
4611 116.0279 2387399.0 4611 116.0279 2387399.0
4612 125.0825 7238442.0 4612 125.0825 7238442.0
4613 150.07768 1073510.0 4613 150.07768 1073510.0
4614 152.09319 544524.0 4614 152.09319 544524.0
4615 156.03424 386143.0 4615 156.03424 386143.0
4616 156.05936 523005.0 4616 156.05936 523005.0
4617 158.04967 579874.0 4617 158.04967 579874.0
4618 170.04977 30639952.0 4618 170.04977 30639952.0
4619 198.08067 12326767.0 4619 198.08067 12326767.0
4620 212.09639 2176296.0 4620 212.09639 2176296.0
4621 230.10741 452827.0 4621 230.10741 452827.0
4622 240.1284 1276547.0 4622 240.1284 1276547.0
4623 4623
4624 COMPOUND_NAME: Metribuzin
4624 SCANNUMBER: 1932 4625 SCANNUMBER: 1932
4625 IONMODE: Positive 4626 IONMODE: Positive
4626 SPECTRUMTYPE: Centroid 4627 SPECTRUMTYPE: Centroid
4627 FORMULA: C8H14N4OS 4628 FORMULA: C8H14N4OS
4628 INCHIKEY: FOXFZRUHNHCZPX-UHFFFAOYSA-N 4629 INCHIKEY: FOXFZRUHNHCZPX-UHFFFAOYSA-N
4631 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4632 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4632 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4633 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4633 IONIZATION: ESI+ 4634 IONIZATION: ESI+
4634 LICENSE: CC BY-NC 4635 LICENSE: CC BY-NC
4635 COMMENT: 4636 COMMENT:
4636 COMPOUND_NAME: Metribuzin
4637 RETENTION_TIME: 4.458099 4637 RETENTION_TIME: 4.458099
4638 PRECURSOR_MZ: 215.0965 4638 PRECURSOR_MZ: 215.0965
4639 ADDUCT: [M+H]+ 4639 ADDUCT: [M+H]+
4640 COLLISION_ENERGY: 4640 COLLISION_ENERGY:
4641 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4641 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4642 NUM PEAKS: 62 4642 NUM PEAKS: 62
4643 85.08886 22454.0 4643 85.08886 22454.0
4644 87.00137 169483.0 4644 87.00137 169483.0
4645 88.00926 84542.0 4645 88.00926 84542.0
4646 89.01718 426359.0 4646 89.01718 426359.0
4647 95.06072 92527.0 4647 95.06072 92527.0
4648 96.04461 50118.0 4648 96.04461 50118.0
4649 97.06514 96987.0 4649 97.06514 96987.0
4650 98.05901 20223.0 4650 98.05901 20223.0
4651 99.09205 39234.0 4651 99.09205 39234.0
4652 104.02791 100681.0 4652 104.02791 100681.0
4653 108.06841 101836.0 4653 108.06841 101836.0
4654 109.07641 56085.0 4654 109.07641 56085.0
4655 110.06014 53533.0 4655 110.06014 53533.0
4656 110.08431 26239.0 4656 110.08431 26239.0
4657 114.03733 55997.0 4657 114.03733 55997.0
4658 114.99636 118244.0 4658 114.99636 118244.0
4659 115.0202 36933.0 4659 115.0202 36933.0
4660 116.01549 91102.0 4660 116.01549 91102.0
4661 117.01186 22228.0 4661 117.01186 22228.0
4662 123.05569 75674.0 4662 123.05569 75674.0
4663 123.07951 19671.0 4663 123.07951 19671.0
4664 124.06344 40346.0 4664 124.06344 40346.0
4665 124.08718 18832.0 4665 124.08718 18832.0
4666 125.07124 54613.0 4666 125.07124 54613.0
4667 125.0825 115086.0 4667 125.0825 115086.0
4668 126.10277 28501.0 4668 126.10277 28501.0
4669 129.03598 19818.0 4669 129.03598 19818.0
4670 130.03105 252134.0 4670 130.03105 252134.0
4671 131.0276 22354.0 4671 131.0276 22354.0
4672 131.03888 1631897.0 4672 131.03888 1631897.0
4673 139.03265 27241.0 4673 139.03265 27241.0
4674 139.09824 52072.0 4674 139.09824 52072.0
4675 140.04034 101100.0 4675 140.04034 101100.0
4676 141.03566 33429.0 4676 141.03566 33429.0
4677 141.04825 19469.0 4677 141.04825 19469.0
4678 143.06389 91872.0 4678 143.06389 91872.0
4679 144.03552 36694.0 4679 144.03552 36694.0
4680 145.05458 227341.0 4680 145.05458 227341.0
4681 147.91982 56049.0 4681 147.91982 56049.0
4682 147.93188 52360.0 4682 147.93188 52360.0
4683 147.93575 42677.0 4683 147.93575 42677.0
4684 147.94106 55028.0 4684 147.94106 55028.0
4685 153.07755 94895.0 4685 153.07755 94895.0
4686 154.04378 27710.0 4686 154.04378 27710.0
4687 155.05132 25496.0 4687 155.05132 25496.0
4688 155.06427 49916.0 4688 155.06427 49916.0
4689 156.05936 708006.0 4689 156.05936 708006.0
4690 157.04344 120558.0 4690 157.04344 120558.0
4691 157.05453 30768.0 4691 157.05453 30768.0
4692 168.02261 18988.0 4692 168.02261 18988.0
4693 170.07477 29338.0 4693 170.07477 29338.0
4694 171.05882 968992.0 4694 171.05882 968992.0
4695 171.07022 30976.0 4695 171.07022 30976.0
4696 171.08282 34546.0 4696 171.08282 34546.0
4697 172.07808 172693.0 4697 172.07808 172693.0
4698 173.50877 74710.0 4698 173.50877 74710.0
4699 182.03879 33707.0 4699 182.03879 33707.0
4700 183.04619 29308.0 4700 183.04619 29308.0
4701 184.05394 333698.0 4701 184.05394 333698.0
4702 186.08231 47791.0 4702 186.08231 47791.0
4703 187.10153 1851092.0 4703 187.10153 1851092.0
4704 215.09644 112225.0 4704 215.09644 112225.0
4705 4705
4706 COMPOUND_NAME: Prometryne
4706 SCANNUMBER: 2407 4707 SCANNUMBER: 2407
4707 IONMODE: Positive 4708 IONMODE: Positive
4708 SPECTRUMTYPE: Centroid 4709 SPECTRUMTYPE: Centroid
4709 FORMULA: C10H19N5S 4710 FORMULA: C10H19N5S
4710 INCHIKEY: AAEVYOVXGOFMJO-UHFFFAOYSA-N 4711 INCHIKEY: AAEVYOVXGOFMJO-UHFFFAOYSA-N
4713 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4714 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4714 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4715 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4715 IONIZATION: ESI+ 4716 IONIZATION: ESI+
4716 LICENSE: CC BY-NC 4717 LICENSE: CC BY-NC
4717 COMMENT: 4718 COMMENT:
4718 COMPOUND_NAME: Prometryne
4719 RETENTION_TIME: 4.990861 4719 RETENTION_TIME: 4.990861
4720 PRECURSOR_MZ: 242.1439 4720 PRECURSOR_MZ: 242.1439
4721 ADDUCT: [M+H]+ 4721 ADDUCT: [M+H]+
4722 COLLISION_ENERGY: 4722 COLLISION_ENERGY:
4723 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4723 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4724 NUM PEAKS: 15 4724 NUM PEAKS: 15
4725 85.05116 4457818.0 4725 85.05116 4457818.0
4726 91.03273 8009682.0 4726 91.03273 8009682.0
4727 96.05572 6069758.0 4727 96.05572 6069758.0
4728 102.03746 367626.0 4728 102.03746 367626.0
4729 110.04619 4165152.0 4729 110.04619 4165152.0
4730 110.0716 444450.0 4730 110.0716 444450.0
4731 113.0825 1093208.0 4731 113.0825 1093208.0
4732 116.0279 11189147.0 4732 116.0279 11189147.0
4733 138.07761 4951850.0 4733 138.07761 4951850.0
4734 144.05917 3781341.0 4734 144.05917 3781341.0
4735 158.04646 408855.0 4735 158.04646 408855.0
4736 158.04967 34215304.0 4736 158.04967 34215304.0
4737 173.50693 425480.0 4737 173.50693 425480.0
4738 186.08095 16656961.0 4738 186.08095 16656961.0
4739 200.09659 2036050.0 4739 200.09659 2036050.0
4740 4740
4741 COMPOUND_NAME: Pyridaben
4741 SCANNUMBER: 8415 4742 SCANNUMBER: 8415
4742 IONMODE: Positive 4743 IONMODE: Positive
4743 SPECTRUMTYPE: Centroid 4744 SPECTRUMTYPE: Centroid
4744 FORMULA: C19H25N2OClS 4745 FORMULA: C19H25N2OClS
4745 INCHIKEY: DWFZBUWUXWZWKD-UHFFFAOYSA-N 4746 INCHIKEY: DWFZBUWUXWZWKD-UHFFFAOYSA-N
4748 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4749 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4749 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4750 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4750 IONIZATION: ESI+ 4751 IONIZATION: ESI+
4751 LICENSE: CC BY-NC 4752 LICENSE: CC BY-NC
4752 COMMENT: 4753 COMMENT:
4753 COMPOUND_NAME: Pyridaben
4754 RETENTION_TIME: 7.556859 4754 RETENTION_TIME: 7.556859
4755 PRECURSOR_MZ: 365.1459 4755 PRECURSOR_MZ: 365.1459
4756 ADDUCT: [M+H]+ 4756 ADDUCT: [M+H]+
4757 COLLISION_ENERGY: 4757 COLLISION_ENERGY:
4758 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4758 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4759 NUM PEAKS: 3 4759 NUM PEAKS: 3
4760 147.11726 1746679.0 4760 147.11726 1746679.0
4761 309.0834 39061400.0 4761 309.0834 39061400.0
4762 365.14478 6893662.0 4762 365.14478 6893662.0
4763 4763
4764 COMPOUND_NAME: Simetryn
4764 SCANNUMBER: 1608 4765 SCANNUMBER: 1608
4765 IONMODE: Positive 4766 IONMODE: Positive
4766 SPECTRUMTYPE: Centroid 4767 SPECTRUMTYPE: Centroid
4767 FORMULA: C8H15N5S 4768 FORMULA: C8H15N5S
4768 INCHIKEY: MGLWZSOBALDPEK-UHFFFAOYSA-N 4769 INCHIKEY: MGLWZSOBALDPEK-UHFFFAOYSA-N
4771 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4772 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4772 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4773 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4773 IONIZATION: ESI+ 4774 IONIZATION: ESI+
4774 LICENSE: CC BY-NC 4775 LICENSE: CC BY-NC
4775 COMMENT: 4776 COMMENT:
4776 COMPOUND_NAME: Simetryn
4777 RETENTION_TIME: 3.75983 4777 RETENTION_TIME: 3.75983
4778 PRECURSOR_MZ: 214.1124 4778 PRECURSOR_MZ: 214.1124
4779 ADDUCT: [M+H]+ 4779 ADDUCT: [M+H]+
4780 COLLISION_ENERGY: 4780 COLLISION_ENERGY:
4781 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4781 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4782 NUM PEAKS: 12 4782 NUM PEAKS: 12
4783 91.03273 299056.0 4783 91.03273 299056.0
4784 96.05597 10435853.0 4784 96.05597 10435853.0
4785 102.03746 159989.0 4785 102.03746 159989.0
4786 113.0825 349517.0 4786 113.0825 349517.0
4787 116.0279 6039216.0 4787 116.0279 6039216.0
4788 124.08718 4340512.0 4788 124.08718 4340512.0
4789 138.07761 424357.0 4789 138.07761 424357.0
4790 144.05917 2698291.0 4790 144.05917 2698291.0
4791 158.04967 123923.0 4791 158.04967 123923.0
4792 166.10905 576911.0 4792 166.10905 576911.0
4793 186.08095 411980.0 4793 186.08095 411980.0
4794 214.11266 506708.0 4794 214.11266 506708.0
4795 4795
4796 COMPOUND_NAME: Sulfentrazone
4796 SCANNUMBER: 2110 4797 SCANNUMBER: 2110
4797 IONMODE: Positive 4798 IONMODE: Positive
4798 SPECTRUMTYPE: Centroid 4799 SPECTRUMTYPE: Centroid
4799 FORMULA: C11H10N4O3Cl2F2S 4800 FORMULA: C11H10N4O3Cl2F2S
4800 INCHIKEY: OORLZFUTLGXMEF-UHFFFAOYSA-N 4801 INCHIKEY: OORLZFUTLGXMEF-UHFFFAOYSA-N
4803 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4804 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4804 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4805 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4805 IONIZATION: ESI+ 4806 IONIZATION: ESI+
4806 LICENSE: CC BY-NC 4807 LICENSE: CC BY-NC
4807 COMMENT: 4808 COMMENT:
4808 COMPOUND_NAME: Sulfentrazone
4809 RETENTION_TIME: 4.825635 4809 RETENTION_TIME: 4.825635
4810 PRECURSOR_MZ: 386.99 4810 PRECURSOR_MZ: 386.99
4811 ADDUCT: [M+H]+ 4811 ADDUCT: [M+H]+
4812 COLLISION_ENERGY: 4812 COLLISION_ENERGY:
4813 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4813 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4814 NUM PEAKS: 48 4814 NUM PEAKS: 48
4815 92.03084 36986.0 4815 92.03084 36986.0
4816 109.9793 24541.0 4816 109.9793 24541.0
4817 111.99506 13105.0 4817 111.99506 13105.0
4818 127.99009 18850.0 4818 127.99009 18850.0
4819 136.99023 73690.0 4819 136.99023 73690.0
4820 139.00583 127950.0 4820 139.00583 127950.0
4821 145.95616 142592.0 4821 145.95616 142592.0
4822 146.00066 61013.0 4822 146.00066 61013.0
4823 146.96414 17631.0 4823 146.96414 17631.0
4824 149.04001 58665.0 4824 149.04001 58665.0
4825 155.00107 516575.0 4825 155.00107 516575.0
4826 157.95639 179021.0 4826 157.95639 179021.0
4827 163.96677 638082.0 4827 163.96677 638082.0
4828 172.96719 294246.0 4828 172.96719 294246.0
4829 173.50693 15383.0 4829 173.50693 15383.0
4830 173.95125 25670.0 4830 173.95125 25670.0
4831 173.97466 222766.0 4831 173.97466 222766.0
4832 175.96661 26415.0 4832 175.96661 26415.0
4833 178.01723 464585.0 4833 178.01723 464585.0
4834 180.03255 13838.0 4834 180.03255 13838.0
4835 182.01176 108423.0 4835 182.01176 108423.0
4836 186.98276 774653.0 4836 186.98276 774653.0
4837 190.97755 43534.0 4837 190.97755 43534.0
4838 198.94617 336099.0 4838 198.94617 336099.0
4839 200.96233 30494.0 4839 200.96233 30494.0
4840 212.00275 22753.0 4840 212.00275 22753.0
4841 213.9933 128858.0 4841 213.9933 128858.0
4842 218.9523 26640.0 4842 218.9523 26640.0
4843 221.02235 12118.0 4843 221.02235 12118.0
4844 222.03113 12834.0 4844 222.03113 12834.0
4845 223.03876 132014.0 4845 223.03876 132014.0
4846 226.96516 14865.0 4846 226.96516 14865.0
4847 232.00861 308335.0 4847 232.00861 308335.0
4848 245.96388 122236.0 4848 245.96388 122236.0
4849 246.97118 31675.0 4849 246.97118 31675.0
4850 256.99966 41655.0 4850 256.99966 41655.0
4851 258.00772 138182.0 4851 258.00772 138182.0
4852 271.01935 68960.0 4852 271.01935 68960.0
4853 272.02798 110904.0 4853 272.02798 110904.0
4854 273.035 1123625.0 4854 273.035 1123625.0
4855 274.04276 16257.0 4855 274.04276 16257.0
4856 279.98544 298347.0 4856 279.98544 298347.0
4857 286.99054 64325.0 4857 286.99054 64325.0
4858 287.99789 19349.0 4858 287.99789 19349.0
4859 289.03033 15241.0 4859 289.03033 15241.0
4860 306.99692 72556.0 4860 306.99692 72556.0
4861 308.00412 68794.0 4861 308.00412 68794.0
4862 336.99271 19232.0 4862 336.99271 19232.0
4863 4863
4864 COMPOUND_NAME: Terbutryn
4864 SCANNUMBER: 2407 4865 SCANNUMBER: 2407
4865 IONMODE: Positive 4866 IONMODE: Positive
4866 SPECTRUMTYPE: Centroid 4867 SPECTRUMTYPE: Centroid
4867 FORMULA: C10H19N5S 4868 FORMULA: C10H19N5S
4868 INCHIKEY: IROINLKCQGIITA-UHFFFAOYSA-N 4869 INCHIKEY: IROINLKCQGIITA-UHFFFAOYSA-N
4871 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4872 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4872 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4873 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4873 IONIZATION: ESI+ 4874 IONIZATION: ESI+
4874 LICENSE: CC BY-NC 4875 LICENSE: CC BY-NC
4875 COMMENT: 4876 COMMENT:
4876 COMPOUND_NAME: Terbutryn
4877 RETENTION_TIME: 4.990861 4877 RETENTION_TIME: 4.990861
4878 PRECURSOR_MZ: 242.1439 4878 PRECURSOR_MZ: 242.1439
4879 ADDUCT: [M+H]+ 4879 ADDUCT: [M+H]+
4880 COLLISION_ENERGY: 4880 COLLISION_ENERGY:
4881 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4881 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4882 NUM PEAKS: 15 4882 NUM PEAKS: 15
4883 85.05116 4457818.0 4883 85.05116 4457818.0
4884 91.03273 8009682.0 4884 91.03273 8009682.0
4885 96.05572 6069758.0 4885 96.05572 6069758.0
4886 102.03746 367626.0 4886 102.03746 367626.0
4887 110.04619 4165152.0 4887 110.04619 4165152.0
4888 110.0716 444450.0 4888 110.0716 444450.0
4889 113.0825 1093208.0 4889 113.0825 1093208.0
4890 116.0279 11189147.0 4890 116.0279 11189147.0
4891 138.07761 4951850.0 4891 138.07761 4951850.0
4892 144.05917 3781341.0 4892 144.05917 3781341.0
4893 158.04646 408855.0 4893 158.04646 408855.0
4894 158.04967 34215304.0 4894 158.04967 34215304.0
4895 173.50693 425480.0 4895 173.50693 425480.0
4896 186.08095 16656961.0 4896 186.08095 16656961.0
4897 200.09659 2036050.0 4897 200.09659 2036050.0
4898 4898
4899 COMPOUND_NAME: Thiabendazole
4899 SCANNUMBER: 1232 4900 SCANNUMBER: 1232
4900 IONMODE: Positive 4901 IONMODE: Positive
4901 SPECTRUMTYPE: Centroid 4902 SPECTRUMTYPE: Centroid
4902 FORMULA: C10H7N3S 4903 FORMULA: C10H7N3S
4903 INCHIKEY: WJCNZQLZVWNLKY-UHFFFAOYSA-N 4904 INCHIKEY: WJCNZQLZVWNLKY-UHFFFAOYSA-N
4906 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4907 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4907 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4908 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4908 IONIZATION: ESI+ 4909 IONIZATION: ESI+
4909 LICENSE: CC BY-NC 4910 LICENSE: CC BY-NC
4910 COMMENT: 4911 COMMENT:
4911 COMPOUND_NAME: Thiabendazole
4912 RETENTION_TIME: 2.44406 4912 RETENTION_TIME: 2.44406
4913 PRECURSOR_MZ: 202.0437 4913 PRECURSOR_MZ: 202.0437
4914 ADDUCT: [M+H]+ 4914 ADDUCT: [M+H]+
4915 COLLISION_ENERGY: 4915 COLLISION_ENERGY:
4916 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4916 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4917 NUM PEAKS: 7 4917 NUM PEAKS: 7
4918 92.0498 482307.0 4918 92.0498 482307.0
4919 131.06062 3699935.0 4919 131.06062 3699935.0
4920 143.06068 408061.0 4920 143.06068 408061.0
4921 158.07153 301732.0 4921 158.07153 301732.0
4922 170.07179 139529.0 4922 170.07179 139529.0
4923 175.03255 9873992.0 4923 175.03255 9873992.0
4924 202.04396 3731232.0 4924 202.04396 3731232.0
4925 4925
4926 COMPOUND_NAME: Thiacloprid
4926 SCANNUMBER: 1685 4927 SCANNUMBER: 1685
4927 IONMODE: Positive 4928 IONMODE: Positive
4928 SPECTRUMTYPE: Centroid 4929 SPECTRUMTYPE: Centroid
4929 FORMULA: C10H9N4ClS 4930 FORMULA: C10H9N4ClS
4930 INCHIKEY: HOKKPVIRMVDYPB-UHFFFAOYSA-N 4931 INCHIKEY: HOKKPVIRMVDYPB-UHFFFAOYSA-N
4933 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4934 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4934 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4935 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4935 IONIZATION: ESI+ 4936 IONIZATION: ESI+
4936 LICENSE: CC BY-NC 4937 LICENSE: CC BY-NC
4937 COMMENT: 4938 COMMENT:
4938 COMPOUND_NAME: Thiacloprid
4939 RETENTION_TIME: 4.159843 4939 RETENTION_TIME: 4.159843
4940 PRECURSOR_MZ: 253.0315 4940 PRECURSOR_MZ: 253.0315
4941 ADDUCT: [M+H]+ 4941 ADDUCT: [M+H]+
4942 COLLISION_ENERGY: 4942 COLLISION_ENERGY:
4943 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4943 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4944 NUM PEAKS: 6 4944 NUM PEAKS: 6
4945 90.03403 1177314.0 4945 90.03403 1177314.0
4946 91.04182 256154.0 4946 91.04182 256154.0
4947 98.99973 1052050.0 4947 98.99973 1052050.0
4948 108.0446 146293.0 4948 108.0446 146293.0
4949 126.01085 11655971.0 4949 126.01085 11655971.0
4950 144.02113 633179.0 4950 144.02113 633179.0
4951 4951
4952 COMPOUND_NAME: Thiamethoxam
4952 SCANNUMBER: 1108 4953 SCANNUMBER: 1108
4953 IONMODE: Positive 4954 IONMODE: Positive
4954 SPECTRUMTYPE: Centroid 4955 SPECTRUMTYPE: Centroid
4955 FORMULA: C8H10N5O3ClS 4956 FORMULA: C8H10N5O3ClS
4956 INCHIKEY: NWWZPOKUUAIXIW-UHFFFAOYSA-N 4957 INCHIKEY: NWWZPOKUUAIXIW-UHFFFAOYSA-N
4959 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4960 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4960 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4961 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4961 IONIZATION: ESI+ 4962 IONIZATION: ESI+
4962 LICENSE: CC BY-NC 4963 LICENSE: CC BY-NC
4963 COMMENT: 4964 COMMENT:
4964 COMPOUND_NAME: Thiamethoxam
4965 RETENTION_TIME: 2.35524 4965 RETENTION_TIME: 2.35524
4966 PRECURSOR_MZ: 292.0273 4966 PRECURSOR_MZ: 292.0273
4967 ADDUCT: [M+H]+ 4967 ADDUCT: [M+H]+
4968 COLLISION_ENERGY: 4968 COLLISION_ENERGY:
4969 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4969 INSTRUMENT_TYPE: LC-ESI-Orbitrap
4970 NUM PEAKS: 10 4970 NUM PEAKS: 10
4971 131.96729 856494.0 4971 131.96729 856494.0
4972 174.9729 61417.0 4972 174.9729 61417.0
4973 180.04681 65222.0 4973 180.04681 65222.0
4974 181.0547 129376.0 4974 181.0547 129376.0
4975 210.05699 499700.0 4975 210.05699 499700.0
4976 211.06477 3262623.0 4976 211.06477 3262623.0
4977 245.02655 33196.0 4977 245.02655 33196.0
4978 246.0343 359117.0 4978 246.0343 359117.0
4979 248.02554 112237.0 4979 248.02554 112237.0
4980 292.02722 584625.0 4980 292.02722 584625.0
4981 4981
4982 COMPOUND_NAME: Tricyclazole
4982 SCANNUMBER: 2638 4983 SCANNUMBER: 2638
4983 IONMODE: Positive 4984 IONMODE: Positive
4984 SPECTRUMTYPE: Centroid 4985 SPECTRUMTYPE: Centroid
4985 FORMULA: C9H7N3S 4986 FORMULA: C9H7N3S
4986 INCHIKEY: DQJCHOQLCLEDLL-UHFFFAOYSA-N 4987 INCHIKEY: DQJCHOQLCLEDLL-UHFFFAOYSA-N
4989 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 4990 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
4990 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 4991 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
4991 IONIZATION: ESI+ 4992 IONIZATION: ESI+
4992 LICENSE: CC BY-NC 4993 LICENSE: CC BY-NC
4993 COMMENT: 4994 COMMENT:
4994 COMPOUND_NAME: Tricyclazole
4995 RETENTION_TIME: 5.514598 4995 RETENTION_TIME: 5.514598
4996 PRECURSOR_MZ: 190.0439 4996 PRECURSOR_MZ: 190.0439
4997 ADDUCT: [M+H]+ 4997 ADDUCT: [M+H]+
4998 COLLISION_ENERGY: 4998 COLLISION_ENERGY:
4999 INSTRUMENT_TYPE: LC-ESI-Orbitrap 4999 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5000 NUM PEAKS: 10 5000 NUM PEAKS: 10
5001 92.0498 1103195.0 5001 92.0498 1103195.0
5002 109.01101 3220386.0 5002 109.01101 3220386.0
5003 119.06059 619856.0 5003 119.06059 619856.0
5004 127.02138 192273.0 5004 127.02138 192273.0
5005 129.04501 178061.0 5005 129.04501 178061.0
5006 130.04021 316945.0 5006 130.04021 316945.0
5007 136.02161 16492967.0 5007 136.02161 16492967.0
5008 137.01691 212259.0 5008 137.01691 212259.0
5009 163.03258 14491751.0 5009 163.03258 14491751.0
5010 190.04391 4390148.0 5010 190.04391 4390148.0
5011 5011
5012 COMPOUND_NAME: Fenarimol
5012 SCANNUMBER: 2801 5013 SCANNUMBER: 2801
5013 IONMODE: Positive 5014 IONMODE: Positive
5014 SPECTRUMTYPE: Centroid 5015 SPECTRUMTYPE: Centroid
5015 FORMULA: C17H12N2OCl2 5016 FORMULA: C17H12N2OCl2
5016 INCHIKEY: NHOWDZOIZKMVAI-KRWDZBQOSA-N 5017 INCHIKEY: NHOWDZOIZKMVAI-KRWDZBQOSA-N
5019 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5020 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5020 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5021 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5021 IONIZATION: ESI+ 5022 IONIZATION: ESI+
5022 LICENSE: CC BY-NC 5023 LICENSE: CC BY-NC
5023 COMMENT: 5024 COMMENT:
5024 COMPOUND_NAME: Fenarimol
5025 RETENTION_TIME: 6.876775 5025 RETENTION_TIME: 6.876775
5026 PRECURSOR_MZ: 331.0412 5026 PRECURSOR_MZ: 331.0412
5027 ADDUCT: [M+H]+ 5027 ADDUCT: [M+H]+
5028 COLLISION_ENERGY: 5028 COLLISION_ENERGY:
5029 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5029 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5030 NUM PEAKS: 60 5030 NUM PEAKS: 60
5031 129.01041 62692.0 5031 129.01041 62692.0
5032 138.99483 4713270.0 5032 138.99483 4713270.0
5033 139.00581 348352.0 5033 139.00581 348352.0
5034 140.02657 87193.0 5034 140.02657 87193.0
5035 149.01559 101793.0 5035 149.01559 101793.0
5036 156.06877 160067.0 5036 156.06877 160067.0
5037 157.07619 145321.0 5037 157.07619 145321.0
5038 160.97346 447898.0 5038 160.97346 447898.0
5039 161.97681 363570.0 5039 161.97681 363570.0
5040 164.0265 120667.0 5040 164.0265 120667.0
5041 165.07053 109460.0 5041 165.07053 109460.0
5042 178.07843 118150.0 5042 178.07843 118150.0
5043 183.0555 74353.0 5043 183.0555 74353.0
5044 184.06332 56066.0 5044 184.06332 56066.0
5045 185.07138 63091.0 5045 185.07138 63091.0
5046 189.07033 2498508.0 5046 189.07033 2498508.0
5047 192.02161 92048.0 5047 192.02161 92048.0
5048 192.04518 47251.0 5048 192.04518 47251.0
5049 199.0313 150848.0 5049 199.0313 150848.0
5050 200.03886 96007.0 5050 200.03886 96007.0
5051 203.07297 92058.0 5051 203.07297 92058.0
5052 204.08092 678200.0 5052 204.08092 678200.0
5053 205.06487 253030.0 5053 205.06487 253030.0
5054 205.08929 197254.0 5054 205.08929 197254.0
5055 206.07339 64967.0 5055 206.07339 64967.0
5056 212.03918 81877.0 5056 212.03918 81877.0
5057 216.08105 187436.0 5057 216.08105 187436.0
5058 217.06558 157687.0 5058 217.06558 157687.0
5059 219.0323 135275.0 5059 219.0323 135275.0
5060 220.0406 48463.0 5060 220.0406 48463.0
5061 223.03162 1274143.0 5061 223.03162 1274143.0
5062 224.03886 340107.0 5062 224.03886 340107.0
5063 225.04663 54849.0 5063 225.04663 54849.0
5064 231.0923 53552.0 5064 231.0923 53552.0
5065 232.07594 380360.0 5065 232.07594 380360.0
5066 232.09967 52199.0 5066 232.09967 52199.0
5067 232.99239 244669.0 5067 232.99239 244669.0
5068 233.08405 997290.0 5068 233.08405 997290.0
5069 235.00783 124586.0 5069 235.00783 124586.0
5070 238.04195 729158.0 5070 238.04195 729158.0
5071 240.05751 690775.0 5071 240.05751 690775.0
5072 241.04176 517674.0 5072 241.04176 517674.0
5073 241.06586 115853.0 5073 241.06586 115853.0
5074 242.08463 143951.0 5074 242.08463 143951.0
5075 243.09258 198185.0 5075 243.09258 198185.0
5076 250.04214 378960.0 5076 250.04214 378960.0
5077 251.0031 434485.0 5077 251.0031 434485.0
5078 251.02657 76166.0 5078 251.02657 76166.0
5079 251.05006 585923.0 5079 251.05006 585923.0
5080 252.03401 1565574.0 5080 252.03401 1565574.0
5081 259.00827 2379846.0 5081 259.00827 2379846.0
5082 259.08661 47950.0 5082 259.08661 47950.0
5083 266.03717 318342.0 5083 266.03717 318342.0
5084 267.04504 216878.0 5084 267.04504 216878.0
5085 267.06848 215642.0 5085 267.06848 215642.0
5086 268.05276 3869425.0 5086 268.05276 3869425.0
5087 276.03445 91579.0 5087 276.03445 91579.0
5088 277.0527 143152.0 5088 277.0527 143152.0
5089 278.06161 515869.0 5089 278.06161 515869.0
5090 279.06857 114232.0 5090 279.06857 114232.0
5091 5091
5092 COMPOUND_NAME: Fenbuconazole
5092 SCANNUMBER: 3202 5093 SCANNUMBER: 3202
5093 IONMODE: Positive 5094 IONMODE: Positive
5094 SPECTRUMTYPE: Centroid 5095 SPECTRUMTYPE: Centroid
5095 FORMULA: C19H17N4Cl 5096 FORMULA: C19H17N4Cl
5096 INCHIKEY: RQDJADAKIFFEKQ-IBGZPJMESA-N 5097 INCHIKEY: RQDJADAKIFFEKQ-IBGZPJMESA-N
5099 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5100 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5100 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5101 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5101 IONIZATION: ESI+ 5102 IONIZATION: ESI+
5102 LICENSE: CC BY-NC 5103 LICENSE: CC BY-NC
5103 COMMENT: 5104 COMMENT:
5104 COMPOUND_NAME: Fenbuconazole
5105 RETENTION_TIME: 7.045859 5105 RETENTION_TIME: 7.045859
5106 PRECURSOR_MZ: 337.1223 5106 PRECURSOR_MZ: 337.1223
5107 ADDUCT: [M+H]+ 5107 ADDUCT: [M+H]+
5108 COLLISION_ENERGY: 5108 COLLISION_ENERGY:
5109 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5109 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5110 NUM PEAKS: 9 5110 NUM PEAKS: 9
5111 89.03882 491858.0 5111 89.03882 491858.0
5112 91.05441 1708709.0 5112 91.05441 1708709.0
5113 103.05439 763259.0 5113 103.05439 763259.0
5114 125.01532 31583906.0 5114 125.01532 31583906.0
5115 128.062 614101.0 5115 128.062 614101.0
5116 129.07021 1018109.0 5116 129.07021 1018109.0
5117 139.0309 716816.0 5117 139.0309 716816.0
5118 155.06064 335216.0 5118 155.06064 335216.0
5119 163.0309 736285.0 5119 163.0309 736285.0
5120 5120
5121 COMPOUND_NAME: Fluquinconazole
5121 SCANNUMBER: 3422 5122 SCANNUMBER: 3422
5122 IONMODE: Positive 5123 IONMODE: Positive
5123 SPECTRUMTYPE: Centroid 5124 SPECTRUMTYPE: Centroid
5124 FORMULA: C16H8N5OCl2F 5125 FORMULA: C16H8N5OCl2F
5125 INCHIKEY: IJJVMEJXYNJXOJ-UHFFFAOYSA-N 5126 INCHIKEY: IJJVMEJXYNJXOJ-UHFFFAOYSA-N
5128 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5129 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5129 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5130 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5130 IONIZATION: ESI+ 5131 IONIZATION: ESI+
5131 LICENSE: CC BY-NC 5132 LICENSE: CC BY-NC
5132 COMMENT: 5133 COMMENT:
5133 COMPOUND_NAME: Fluquinconazole
5134 RETENTION_TIME: 7.093534 5134 RETENTION_TIME: 7.093534
5135 PRECURSOR_MZ: 376.0173 5135 PRECURSOR_MZ: 376.0173
5136 ADDUCT: [M+H]+ 5136 ADDUCT: [M+H]+
5137 COLLISION_ENERGY: 5137 COLLISION_ENERGY:
5138 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5138 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5139 NUM PEAKS: 22 5139 NUM PEAKS: 22
5140 108.02471 848273.0 5140 108.02471 848273.0
5141 123.99523 983397.0 5141 123.99523 983397.0
5142 126.03514 85852.0 5142 126.03514 85852.0
5143 158.97679 294325.0 5143 158.97679 294325.0
5144 163.03033 1264696.0 5144 163.03033 1264696.0
5145 181.04097 120423.0 5145 181.04097 120423.0
5146 195.05714 105799.0 5146 195.05714 105799.0
5147 243.01224 134077.0 5147 243.01224 134077.0
5148 244.01985 783328.0 5148 244.01985 783328.0
5149 251.97818 94741.0 5149 251.97818 94741.0
5150 272.01474 3792436.0 5150 272.01474 3792436.0
5151 278.98978 1325774.0 5151 278.98978 1325774.0
5152 279.97287 100928.0 5152 279.97287 100928.0
5153 287.02576 171499.0 5153 287.02576 171499.0
5154 306.98392 7738432.0 5154 306.98392 7738432.0
5155 313.02911 148350.0 5155 313.02911 148350.0
5156 314.03632 96754.0 5156 314.03632 96754.0
5157 324.99539 291864.0 5157 324.99539 291864.0
5158 331.97888 91552.0 5158 331.97888 91552.0
5159 339.01056 449848.0 5159 339.01056 449848.0
5160 349.00613 731296.0 5160 349.00613 731296.0
5161 349.98984 271485.0 5161 349.98984 271485.0
5162 5162
5163 COMPOUND_NAME: Flutriafol
5163 SCANNUMBER: 1408 5164 SCANNUMBER: 1408
5164 IONMODE: Positive 5165 IONMODE: Positive
5165 SPECTRUMTYPE: Centroid 5166 SPECTRUMTYPE: Centroid
5166 FORMULA: C16H13N3OF2 5167 FORMULA: C16H13N3OF2
5167 INCHIKEY: JWUCHKBSVLQQCO-INIZCTEOSA-N 5168 INCHIKEY: JWUCHKBSVLQQCO-INIZCTEOSA-N
5170 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5171 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5171 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5172 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5172 IONIZATION: ESI+ 5173 IONIZATION: ESI+
5173 LICENSE: CC BY-NC 5174 LICENSE: CC BY-NC
5174 COMMENT: 5175 COMMENT:
5175 COMPOUND_NAME: Flutriafol
5176 RETENTION_TIME: 5.240544 5176 RETENTION_TIME: 5.240544
5177 PRECURSOR_MZ: 302.1111 5177 PRECURSOR_MZ: 302.1111
5178 ADDUCT: [M+H]+ 5178 ADDUCT: [M+H]+
5179 COLLISION_ENERGY: 5179 COLLISION_ENERGY:
5180 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5180 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5181 NUM PEAKS: 11 5181 NUM PEAKS: 11
5182 109.04492 5549990.0 5182 109.04492 5549990.0
5183 113.03991 603136.0 5183 113.03991 603136.0
5184 123.02199 197823.0 5184 123.02199 197823.0
5185 123.02419 14667272.0 5185 123.02419 14667272.0
5186 123.03517 2231147.0 5186 123.03517 2231147.0
5187 137.03973 187845.0 5187 137.03973 187845.0
5188 165.06996 216662.0 5188 165.06996 216662.0
5189 194.05283 196543.0 5189 194.05283 196543.0
5190 195.06081 577107.0 5190 195.06081 577107.0
5191 214.05884 311976.0 5191 214.05884 311976.0
5192 215.0668 353163.0 5192 215.0668 353163.0
5193 5193
5194 COMPOUND_NAME: Fuberidazole
5194 SCANNUMBER: 1202 5195 SCANNUMBER: 1202
5195 IONMODE: Positive 5196 IONMODE: Positive
5196 SPECTRUMTYPE: Centroid 5197 SPECTRUMTYPE: Centroid
5197 FORMULA: C11H8N2O 5198 FORMULA: C11H8N2O
5198 INCHIKEY: UYJUZNLFJAWNEZ-UHFFFAOYSA-N 5199 INCHIKEY: UYJUZNLFJAWNEZ-UHFFFAOYSA-N
5201 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5202 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5202 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5203 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5203 IONIZATION: ESI+ 5204 IONIZATION: ESI+
5204 LICENSE: CC BY-NC 5205 LICENSE: CC BY-NC
5205 COMMENT: 5206 COMMENT:
5206 COMPOUND_NAME: Fuberidazole
5207 RETENTION_TIME: 2.456748 5207 RETENTION_TIME: 2.456748
5208 PRECURSOR_MZ: 185.0715 5208 PRECURSOR_MZ: 185.0715
5209 ADDUCT: [M+H]+ 5209 ADDUCT: [M+H]+
5210 COLLISION_ENERGY: 5210 COLLISION_ENERGY:
5211 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5211 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5212 NUM PEAKS: 15 5212 NUM PEAKS: 15
5213 92.0498 2714348.0 5213 92.0498 2714348.0
5214 103.05439 924742.0 5214 103.05439 924742.0
5215 118.05279 1356359.0 5215 118.05279 1356359.0
5216 119.06059 1561269.0 5216 119.06059 1561269.0
5217 128.04956 416024.0 5217 128.04956 416024.0
5218 129.04501 934098.0 5218 129.04501 934098.0
5219 129.05762 1711080.0 5219 129.05762 1711080.0
5220 130.06528 5627980.0 5220 130.06528 5627980.0
5221 131.06062 2006719.0 5221 131.06062 2006719.0
5222 142.05298 1703655.0 5222 142.05298 1703655.0
5223 143.06068 769483.0 5223 143.06068 769483.0
5224 155.06064 2222038.0 5224 155.06064 2222038.0
5225 156.06877 35950644.0 5225 156.06877 35950644.0
5226 157.07619 39653584.0 5226 157.07619 39653584.0
5227 185.0714 6790632.0 5227 185.0714 6790632.0
5228 5228
5229 COMPOUND_NAME: Cyproconazole_1
5229 SCANNUMBER: 1619 5230 SCANNUMBER: 1619
5230 IONMODE: Positive 5231 IONMODE: Positive
5231 SPECTRUMTYPE: Centroid 5232 SPECTRUMTYPE: Centroid
5232 FORMULA: C15H18N3OCl 5233 FORMULA: C15H18N3OCl
5233 INCHIKEY: UFNOUKDBUJZYDE-UHFFFAOYSA-N 5234 INCHIKEY: UFNOUKDBUJZYDE-UHFFFAOYSA-N
5236 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5237 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5237 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5238 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5238 IONIZATION: ESI+ 5239 IONIZATION: ESI+
5239 LICENSE: CC BY-NC 5240 LICENSE: CC BY-NC
5240 COMMENT: 5241 COMMENT:
5241 COMPOUND_NAME: Cyproconazole_1
5242 RETENTION_TIME: 6.138374 5242 RETENTION_TIME: 6.138374
5243 PRECURSOR_MZ: 292.122 5243 PRECURSOR_MZ: 292.122
5244 ADDUCT: [M+H]+ 5244 ADDUCT: [M+H]+
5245 COLLISION_ENERGY: 5245 COLLISION_ENERGY:
5246 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5246 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5247 NUM PEAKS: 4 5247 NUM PEAKS: 4
5248 89.03882 111896.0 5248 89.03882 111896.0
5249 125.01532 6537308.0 5249 125.01532 6537308.0
5250 138.99483 329090.0 5250 138.99483 329090.0
5251 139.00581 166501.0 5251 139.00581 166501.0
5252 5252
5253 COMPOUND_NAME: Cyproconazole_2
5253 SCANNUMBER: 1786 5254 SCANNUMBER: 1786
5254 IONMODE: Positive 5255 IONMODE: Positive
5255 SPECTRUMTYPE: Centroid 5256 SPECTRUMTYPE: Centroid
5256 FORMULA: C15H18N3OCl 5257 FORMULA: C15H18N3OCl
5257 INCHIKEY: UFNOUKDBUJZYDE-UHFFFAOYSA-N 5258 INCHIKEY: UFNOUKDBUJZYDE-UHFFFAOYSA-N
5260 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5261 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5261 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5262 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5262 IONIZATION: ESI+ 5263 IONIZATION: ESI+
5263 LICENSE: CC BY-NC 5264 LICENSE: CC BY-NC
5264 COMMENT: 5265 COMMENT:
5265 COMPOUND_NAME: Cyproconazole_2
5266 RETENTION_TIME: 6.36811 5266 RETENTION_TIME: 6.36811
5267 PRECURSOR_MZ: 292.1225 5267 PRECURSOR_MZ: 292.1225
5268 ADDUCT: [M+H]+ 5268 ADDUCT: [M+H]+
5269 COLLISION_ENERGY: 5269 COLLISION_ENERGY:
5270 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5270 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5271 NUM PEAKS: 4 5271 NUM PEAKS: 4
5272 89.03882 144933.0 5272 89.03882 144933.0
5273 125.01532 8553550.0 5273 125.01532 8553550.0
5274 138.99483 403028.0 5274 138.99483 403028.0
5275 139.00581 198856.0 5275 139.00581 198856.0
5276 5276
5277 COMPOUND_NAME: Diclobutrazol
5277 SCANNUMBER: 2657 5278 SCANNUMBER: 2657
5278 IONMODE: Positive 5279 IONMODE: Positive
5279 SPECTRUMTYPE: Centroid 5280 SPECTRUMTYPE: Centroid
5280 FORMULA: C15H19N3OCl2 5281 FORMULA: C15H19N3OCl2
5281 INCHIKEY: URDNHJIVMYZFRT-UHFFFAOYSA-N 5282 INCHIKEY: URDNHJIVMYZFRT-UHFFFAOYSA-N
5284 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5285 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5285 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5286 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5286 IONIZATION: ESI+ 5287 IONIZATION: ESI+
5287 LICENSE: CC BY-NC 5288 LICENSE: CC BY-NC
5288 COMMENT: 5289 COMMENT:
5289 COMPOUND_NAME: Diclobutrazol
5290 RETENTION_TIME: 6.830443 5290 RETENTION_TIME: 6.830443
5291 PRECURSOR_MZ: 328.0983 5291 PRECURSOR_MZ: 328.0983
5292 ADDUCT: [M+H]+ 5292 ADDUCT: [M+H]+
5293 COLLISION_ENERGY: 5293 COLLISION_ENERGY:
5294 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5294 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5295 NUM PEAKS: 11 5295 NUM PEAKS: 11
5296 122.99965 485826.0 5296 122.99965 485826.0
5297 125.01532 529574.0 5297 125.01532 529574.0
5298 137.01562 496542.0 5298 137.01562 496542.0
5299 158.97626 45675696.0 5299 158.97626 45675696.0
5300 164.03891 599051.0 5300 164.03891 599051.0
5301 172.9556 1689517.0 5301 172.9556 1689517.0
5302 172.99223 1044544.0 5302 172.99223 1044544.0
5303 174.97104 486149.0 5303 174.97104 486149.0
5304 186.97108 498843.0 5304 186.97108 498843.0
5305 190.96622 746907.0 5305 190.96622 746907.0
5306 199.00793 579087.0 5306 199.00793 579087.0
5307 5307
5308 COMPOUND_NAME: Difenoconazole
5308 SCANNUMBER: 4342 5309 SCANNUMBER: 4342
5309 IONMODE: Positive 5310 IONMODE: Positive
5310 SPECTRUMTYPE: Centroid 5311 SPECTRUMTYPE: Centroid
5311 FORMULA: C19H17N3O3Cl2 5312 FORMULA: C19H17N3O3Cl2
5312 INCHIKEY: BQYJATMQXGBDHF-UHFFFAOYSA-N 5313 INCHIKEY: BQYJATMQXGBDHF-UHFFFAOYSA-N
5315 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5316 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5316 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5317 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5317 IONIZATION: ESI+ 5318 IONIZATION: ESI+
5318 LICENSE: CC BY-NC 5319 LICENSE: CC BY-NC
5319 COMMENT: 5320 COMMENT:
5320 COMPOUND_NAME: Difenoconazole
5321 RETENTION_TIME: 7.351549 5321 RETENTION_TIME: 7.351549
5322 PRECURSOR_MZ: 406.0727 5322 PRECURSOR_MZ: 406.0727
5323 ADDUCT: [M+H]+ 5323 ADDUCT: [M+H]+
5324 COLLISION_ENERGY: 5324 COLLISION_ENERGY:
5325 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5325 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5326 NUM PEAKS: 13 5326 NUM PEAKS: 13
5327 129.07021 341601.0 5327 129.07021 341601.0
5328 139.00626 338485.0 5328 139.00626 338485.0
5329 141.01048 334473.0 5329 141.01048 334473.0
5330 152.06247 924840.0 5330 152.06247 924840.0
5331 153.07042 500230.0 5331 153.07042 500230.0
5332 181.06517 598188.0 5332 181.06517 598188.0
5333 187.03149 1315167.0 5333 187.03149 1315167.0
5334 188.03915 3752594.0 5334 188.03915 3752594.0
5335 215.02702 454036.0 5335 215.02702 454036.0
5336 216.03418 363614.0 5336 216.03418 363614.0
5337 223.00838 2665156.0 5337 223.00838 2665156.0
5338 251.0031 32513990.0 5338 251.0031 32513990.0
5339 264.98291 3756956.0 5339 264.98291 3756956.0
5340 5340
5341 COMPOUND_NAME: Diniconazole
5341 SCANNUMBER: 3119 5342 SCANNUMBER: 3119
5342 IONMODE: Positive 5343 IONMODE: Positive
5343 SPECTRUMTYPE: Centroid 5344 SPECTRUMTYPE: Centroid
5344 FORMULA: C15H17N3OCl2 5345 FORMULA: C15H17N3OCl2
5345 INCHIKEY: FBOUIAKEJMZPQG-CQSZACIVSA-N 5346 INCHIKEY: FBOUIAKEJMZPQG-CQSZACIVSA-N
5348 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5349 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5349 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5350 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5350 IONIZATION: ESI+ 5351 IONIZATION: ESI+
5351 LICENSE: CC BY-NC 5352 LICENSE: CC BY-NC
5352 COMMENT: 5353 COMMENT:
5353 COMPOUND_NAME: Diniconazole
5354 RETENTION_TIME: 6.999194 5354 RETENTION_TIME: 6.999194
5355 PRECURSOR_MZ: 326.0832 5355 PRECURSOR_MZ: 326.0832
5356 ADDUCT: [M+H]+ 5356 ADDUCT: [M+H]+
5357 COLLISION_ENERGY: 5357 COLLISION_ENERGY:
5358 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5358 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5359 NUM PEAKS: 52 5359 NUM PEAKS: 52
5360 87.0807 115189.0 5360 87.0807 115189.0
5361 110.0716 52760.0 5361 110.0716 52760.0
5362 123.00002 65949.0 5362 123.00002 65949.0
5363 136.00755 116731.0 5363 136.00755 116731.0
5364 137.01562 125799.0 5364 137.01562 125799.0
5365 141.07028 87788.0 5365 141.07028 87788.0
5366 143.08594 53581.0 5366 143.08594 53581.0
5367 145.0649 52799.0 5367 145.0649 52799.0
5368 148.08749 54447.0 5368 148.08749 54447.0
5369 150.02344 61653.0 5369 150.02344 61653.0
5370 153.07042 57255.0 5370 153.07042 57255.0
5371 154.07816 75541.0 5371 154.07816 75541.0
5372 158.97679 4013011.0 5372 158.97679 4013011.0
5373 162.0233 223821.0 5373 162.0233 223821.0
5374 164.03891 43958.0 5374 164.03891 43958.0
5375 165.01022 141964.0 5375 165.01022 141964.0
5376 166.0183 79777.0 5376 166.0183 79777.0
5377 169.10155 324107.0 5377 169.10155 324107.0
5378 170.97658 348553.0 5378 170.97658 348553.0
5379 172.95621 929271.0 5379 172.95621 929271.0
5380 172.96719 160833.0 5380 172.96719 160833.0
5381 172.99223 196389.0 5381 172.99223 196389.0
5382 175.0313 83110.0 5382 175.0313 83110.0
5383 176.03931 389366.0 5383 176.03931 389366.0
5384 179.02609 125863.0 5384 179.02609 125863.0
5385 180.03384 98155.0 5385 180.03384 98155.0
5386 182.07175 55824.0 5386 182.07175 55824.0
5387 182.97643 126111.0 5387 182.97643 126111.0
5388 184.99236 46623.0 5388 184.99236 46623.0
5389 185.98766 43685.0 5389 185.98766 43685.0
5390 189.0215 81465.0 5390 189.0215 81465.0
5391 189.04662 463062.0 5391 189.04662 463062.0
5392 190.02985 105876.0 5392 190.02985 105876.0
5393 191.02502 124599.0 5393 191.02502 124599.0
5394 193.04185 237565.0 5394 193.04185 237565.0
5395 196.99208 133380.0 5395 196.99208 133380.0
5396 203.03725 47288.0 5396 203.03725 47288.0
5397 203.06287 40626.0 5397 203.06287 40626.0
5398 204.07076 337511.0 5398 204.07076 337511.0
5399 205.01678 42726.0 5399 205.01678 42726.0
5400 207.0574 131489.0 5400 207.0574 131489.0
5401 209.9998 62865.0 5401 209.9998 62865.0
5402 216.03247 187324.0 5402 216.03247 187324.0
5403 217.0407 287524.0 5403 217.0407 287524.0
5404 224.01547 69804.0 5404 224.01547 69804.0
5405 230.04839 54464.0 5405 230.04839 54464.0
5406 234.04297 67828.0 5406 234.04297 67828.0
5407 240.0096 86885.0 5407 240.0096 86885.0
5408 252.00932 126391.0 5408 252.00932 126391.0
5409 264.0097 43206.0 5409 264.0097 43206.0
5410 270.01987 48934.0 5410 270.01987 48934.0
5411 278.02554 102202.0 5411 278.02554 102202.0
5412 5412
5413 COMPOUND_NAME: Epoxiconazole
5413 SCANNUMBER: 3124 5414 SCANNUMBER: 3124
5414 IONMODE: Positive 5415 IONMODE: Positive
5415 SPECTRUMTYPE: Centroid 5416 SPECTRUMTYPE: Centroid
5416 FORMULA: C17H13N3OClF 5417 FORMULA: C17H13N3OClF
5417 INCHIKEY: ZMYFCFLJBGAQRS-IAGOWNOFSA-N 5418 INCHIKEY: ZMYFCFLJBGAQRS-IAGOWNOFSA-N
5420 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5421 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5421 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5422 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5422 IONIZATION: ESI+ 5423 IONIZATION: ESI+
5423 LICENSE: CC BY-NC 5424 LICENSE: CC BY-NC
5424 COMMENT: 5425 COMMENT:
5425 COMPOUND_NAME: Epoxiconazole
5426 RETENTION_TIME: 6.999194 5426 RETENTION_TIME: 6.999194
5427 PRECURSOR_MZ: 330.0806 5427 PRECURSOR_MZ: 330.0806
5428 ADDUCT: [M+H]+ 5428 ADDUCT: [M+H]+
5429 COLLISION_ENERGY: 5429 COLLISION_ENERGY:
5430 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5430 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5431 NUM PEAKS: 12 5431 NUM PEAKS: 12
5432 91.05464 783917.0 5432 91.05464 783917.0
5433 101.03878 454726.0 5433 101.03878 454726.0
5434 113.01572 623551.0 5434 113.01572 623551.0
5435 113.04023 604178.0 5435 113.04023 604178.0
5436 119.04978 1591248.0 5436 119.04978 1591248.0
5437 121.04307 362239.0 5437 121.04307 362239.0
5438 121.04521 27069946.0 5438 121.04521 27069946.0
5439 123.02455 5942544.0 5439 123.02455 5942544.0
5440 123.03517 2030362.0 5440 123.03517 2030362.0
5441 129.04501 7068444.0 5441 129.04501 7068444.0
5442 138.99483 468356.0 5442 138.99483 468356.0
5443 141.01048 1219612.0 5443 141.01048 1219612.0
5444 5444
5445 COMPOUND_NAME: Etaconazole
5445 SCANNUMBER: 2581 5446 SCANNUMBER: 2581
5446 IONMODE: Positive 5447 IONMODE: Positive
5447 SPECTRUMTYPE: Centroid 5448 SPECTRUMTYPE: Centroid
5448 FORMULA: C14H15N3O2Cl2 5449 FORMULA: C14H15N3O2Cl2
5449 INCHIKEY: DWRKFAJEBUWTQM-UHFFFAOYSA-N 5450 INCHIKEY: DWRKFAJEBUWTQM-UHFFFAOYSA-N
5452 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5453 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5453 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5454 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5454 IONIZATION: ESI+ 5455 IONIZATION: ESI+
5455 LICENSE: CC BY-NC 5456 LICENSE: CC BY-NC
5456 COMMENT: 5457 COMMENT:
5457 COMPOUND_NAME: Etaconazole
5458 RETENTION_TIME: 6.802904 5458 RETENTION_TIME: 6.802904
5459 PRECURSOR_MZ: 328.0626 5459 PRECURSOR_MZ: 328.0626
5460 ADDUCT: [M+H]+ 5460 ADDUCT: [M+H]+
5461 COLLISION_ENERGY: 5461 COLLISION_ENERGY:
5462 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5462 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5463 NUM PEAKS: 10 5463 NUM PEAKS: 10
5464 122.99965 480348.0 5464 122.99965 480348.0
5465 125.01532 599928.0 5465 125.01532 599928.0
5466 137.01562 455760.0 5466 137.01562 455760.0
5467 158.97626 39434140.0 5467 158.97626 39434140.0
5468 164.03891 610435.0 5468 164.03891 610435.0
5469 172.9556 1469728.0 5469 172.9556 1469728.0
5470 172.99223 970218.0 5470 172.99223 970218.0
5471 174.97166 597883.0 5471 174.97166 597883.0
5472 190.96622 527039.0 5472 190.96622 527039.0
5473 199.00793 567443.0 5473 199.00793 567443.0
5474 5474
5475 COMPOUND_NAME: Ethirimol
5475 SCANNUMBER: 1043 5476 SCANNUMBER: 1043
5476 IONMODE: Positive 5477 IONMODE: Positive
5477 SPECTRUMTYPE: Centroid 5478 SPECTRUMTYPE: Centroid
5478 FORMULA: C11H19N3O 5479 FORMULA: C11H19N3O
5479 INCHIKEY: BBXXLROWFHWFQY-UHFFFAOYSA-N 5480 INCHIKEY: BBXXLROWFHWFQY-UHFFFAOYSA-N
5482 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5483 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5483 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5484 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5484 IONIZATION: ESI+ 5485 IONIZATION: ESI+
5485 LICENSE: CC BY-NC 5486 LICENSE: CC BY-NC
5486 COMMENT: 5487 COMMENT:
5487 COMPOUND_NAME: Ethirimol
5488 RETENTION_TIME: 2.246086 5488 RETENTION_TIME: 2.246086
5489 PRECURSOR_MZ: 210.1608 5489 PRECURSOR_MZ: 210.1608
5490 ADDUCT: [M+H]+ 5490 ADDUCT: [M+H]+
5491 COLLISION_ENERGY: 5491 COLLISION_ENERGY:
5492 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5492 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5493 NUM PEAKS: 32 5493 NUM PEAKS: 32
5494 93.07027 325229.0 5494 93.07027 325229.0
5495 95.06072 869968.0 5495 95.06072 869968.0
5496 95.08585 891568.0 5496 95.08585 891568.0
5497 96.0446 781962.0 5497 96.0446 781962.0
5498 97.03999 1008744.0 5498 97.03999 1008744.0
5499 98.06031 16588468.0 5499 98.06031 16588468.0
5500 105.07019 215544.0 5500 105.07019 215544.0
5501 107.07314 1858556.0 5501 107.07314 1858556.0
5502 109.0761 345145.0 5502 109.0761 345145.0
5503 110.06044 242964.0 5503 110.06044 242964.0
5504 110.0716 341679.0 5504 110.0716 341679.0
5505 110.09671 170712.0 5505 110.09671 170712.0
5506 111.07922 353713.0 5506 111.07922 353713.0
5507 112.11221 261603.0 5507 112.11221 261603.0
5508 114.06642 269861.0 5508 114.06642 269861.0
5509 120.081 391118.0 5509 120.081 391118.0
5510 122.07138 761007.0 5510 122.07138 761007.0
5511 122.08405 230087.0 5511 122.08405 230087.0
5512 122.09672 693029.0 5512 122.09672 693029.0
5513 123.05569 456004.0 5513 123.05569 456004.0
5514 124.06344 347297.0 5514 124.06344 347297.0
5515 138.06627 3057256.0 5515 138.06627 3057256.0
5516 139.07446 2046408.0 5516 139.07446 2046408.0
5517 140.10709 14705233.0 5517 140.10709 14705233.0
5518 150.10286 1256237.0 5518 150.10286 1256237.0
5519 152.08211 570565.0 5519 152.08211 570565.0
5520 165.10242 2897067.0 5520 165.10242 2897067.0
5521 166.09755 407251.0 5521 166.09755 407251.0
5522 167.10577 1091732.0 5522 167.10577 1091732.0
5523 182.12912 2661313.0 5523 182.12912 2661313.0
5524 193.13402 1554662.0 5524 193.13402 1554662.0
5525 210.15997 2414378.0 5525 210.15997 2414378.0
5526 5526
5527 COMPOUND_NAME: Hexaconazole
5527 SCANNUMBER: 2543 5528 SCANNUMBER: 2543
5528 IONMODE: Positive 5529 IONMODE: Positive
5529 SPECTRUMTYPE: Centroid 5530 SPECTRUMTYPE: Centroid
5530 FORMULA: C14H17N3OCl2 5531 FORMULA: C14H17N3OCl2
5531 INCHIKEY: STMIIPIFODONDC-AWEZNQCLSA-N 5532 INCHIKEY: STMIIPIFODONDC-AWEZNQCLSA-N
5534 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5535 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5535 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5536 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5536 IONIZATION: ESI+ 5537 IONIZATION: ESI+
5537 LICENSE: CC BY-NC 5538 LICENSE: CC BY-NC
5538 COMMENT: 5539 COMMENT:
5539 COMPOUND_NAME: Hexaconazole
5540 RETENTION_TIME: 6.793731 5540 RETENTION_TIME: 6.793731
5541 PRECURSOR_MZ: 314.0833 5541 PRECURSOR_MZ: 314.0833
5542 ADDUCT: [M+H]+ 5542 ADDUCT: [M+H]+
5543 COLLISION_ENERGY: 5543 COLLISION_ENERGY:
5544 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5544 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5545 NUM PEAKS: 16 5545 NUM PEAKS: 16
5546 115.05463 149487.0 5546 115.05463 149487.0
5547 123.00002 104704.0 5547 123.00002 104704.0
5548 125.0157 1580755.0 5548 125.0157 1580755.0
5549 129.01041 156034.0 5549 129.01041 156034.0
5550 136.00755 162737.0 5550 136.00755 162737.0
5551 139.00626 458884.0 5551 139.00626 458884.0
5552 146.97656 554008.0 5552 146.97656 554008.0
5553 149.01559 424582.0 5553 149.01559 424582.0
5554 150.02344 1003022.0 5554 150.02344 1003022.0
5555 153.01047 351412.0 5555 153.01047 351412.0
5556 158.97679 7629371.0 5556 158.97679 7629371.0
5557 170.97658 545468.0 5557 170.97658 545468.0
5558 172.99223 112377.0 5558 172.99223 112377.0
5559 174.97166 740773.0 5559 174.97166 740773.0
5560 184.99236 690533.0 5560 184.99236 690533.0
5561 188.98734 151249.0 5561 188.98734 151249.0
5562 5562
5563 COMPOUND_NAME: Ipconazole
5563 SCANNUMBER: 3476 5564 SCANNUMBER: 3476
5564 IONMODE: Positive 5565 IONMODE: Positive
5565 SPECTRUMTYPE: Centroid 5566 SPECTRUMTYPE: Centroid
5566 FORMULA: C18H24N3OCl 5567 FORMULA: C18H24N3OCl
5567 INCHIKEY: QTYCMDBMOLSEAM-UHFFFAOYSA-N 5568 INCHIKEY: QTYCMDBMOLSEAM-UHFFFAOYSA-N
5570 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5571 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5571 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5572 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5572 IONIZATION: ESI+ 5573 IONIZATION: ESI+
5573 LICENSE: CC BY-NC 5574 LICENSE: CC BY-NC
5574 COMMENT: 5575 COMMENT:
5575 COMPOUND_NAME: Ipconazole
5576 RETENTION_TIME: 7.112235 5576 RETENTION_TIME: 7.112235
5577 PRECURSOR_MZ: 334.1694 5577 PRECURSOR_MZ: 334.1694
5578 ADDUCT: [M+H]+ 5578 ADDUCT: [M+H]+
5579 COLLISION_ENERGY: 5579 COLLISION_ENERGY:
5580 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5580 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5581 NUM PEAKS: 18 5581 NUM PEAKS: 18
5582 89.03882 79221.0 5582 89.03882 79221.0
5583 95.08585 152078.0 5583 95.08585 152078.0
5584 109.10148 351087.0 5584 109.10148 351087.0
5585 115.05463 110112.0 5585 115.05463 110112.0
5586 116.06245 125067.0 5586 116.06245 125067.0
5587 125.01532 7756546.0 5587 125.01532 7756546.0
5588 128.06239 168573.0 5588 128.06239 168573.0
5589 130.078 83461.0 5589 130.078 83461.0
5590 139.03134 219182.0 5590 139.03134 219182.0
5591 142.07797 176298.0 5591 142.07797 176298.0
5592 149.01559 120448.0 5592 149.01559 120448.0
5593 151.03107 544953.0 5593 151.03107 544953.0
5594 155.06064 99629.0 5594 155.06064 99629.0
5595 156.09335 164234.0 5595 156.09335 164234.0
5596 163.0309 672001.0 5596 163.0309 672001.0
5597 165.04663 173374.0 5597 165.04663 173374.0
5598 177.04655 269267.0 5598 177.04655 269267.0
5599 191.06258 291856.0 5599 191.06258 291856.0
5600 5600
5601 COMPOUND_NAME: Metconazole
5601 SCANNUMBER: 3161 5602 SCANNUMBER: 3161
5602 IONMODE: Positive 5603 IONMODE: Positive
5603 SPECTRUMTYPE: Centroid 5604 SPECTRUMTYPE: Centroid
5604 FORMULA: C17H22N3OCl 5605 FORMULA: C17H22N3OCl
5605 INCHIKEY: XWPZUHJBOLQNMN-UHFFFAOYSA-N 5606 INCHIKEY: XWPZUHJBOLQNMN-UHFFFAOYSA-N
5608 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5609 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5609 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5610 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5610 IONIZATION: ESI+ 5611 IONIZATION: ESI+
5611 LICENSE: CC BY-NC 5612 LICENSE: CC BY-NC
5612 COMMENT: 5613 COMMENT:
5613 COMPOUND_NAME: Metconazole
5614 RETENTION_TIME: 7.017605 5614 RETENTION_TIME: 7.017605
5615 PRECURSOR_MZ: 320.1538 5615 PRECURSOR_MZ: 320.1538
5616 ADDUCT: [M+H]+ 5616 ADDUCT: [M+H]+
5617 COLLISION_ENERGY: 5617 COLLISION_ENERGY:
5618 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5618 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5619 NUM PEAKS: 13 5619 NUM PEAKS: 13
5620 95.08585 468079.0 5620 95.08585 468079.0
5621 107.08563 155599.0 5621 107.08563 155599.0
5622 125.01532 7873925.0 5622 125.01532 7873925.0
5623 128.06239 109318.0 5623 128.06239 109318.0
5624 139.0309 414801.0 5624 139.0309 414801.0
5625 141.07028 83342.0 5625 141.07028 83342.0
5626 142.07797 413140.0 5626 142.07797 413140.0
5627 151.03107 437268.0 5627 151.03107 437268.0
5628 156.09335 90865.0 5628 156.09335 90865.0
5629 163.0309 398692.0 5629 163.0309 398692.0
5630 165.04663 82686.0 5630 165.04663 82686.0
5631 177.04655 645875.0 5631 177.04655 645875.0
5632 191.06258 194319.0 5632 191.06258 194319.0
5633 5633
5634 COMPOUND_NAME: Nuarimol
5634 SCANNUMBER: 1883 5635 SCANNUMBER: 1883
5635 IONMODE: Positive 5636 IONMODE: Positive
5636 SPECTRUMTYPE: Centroid 5637 SPECTRUMTYPE: Centroid
5637 FORMULA: C17H12N2OClF 5638 FORMULA: C17H12N2OClF
5638 INCHIKEY: SAPGTCDSBGMXCD-KRWDZBQOSA-N 5639 INCHIKEY: SAPGTCDSBGMXCD-KRWDZBQOSA-N
5641 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5642 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5642 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5643 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5643 IONIZATION: ESI+ 5644 IONIZATION: ESI+
5644 LICENSE: CC BY-NC 5645 LICENSE: CC BY-NC
5645 COMMENT: 5646 COMMENT:
5646 COMPOUND_NAME: Nuarimol
5647 RETENTION_TIME: 6.452959 5647 RETENTION_TIME: 6.452959
5648 PRECURSOR_MZ: 315.0705 5648 PRECURSOR_MZ: 315.0705
5649 ADDUCT: [M+H]+ 5649 ADDUCT: [M+H]+
5650 COLLISION_ENERGY: 5650 COLLISION_ENERGY:
5651 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5651 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5652 NUM PEAKS: 59 5652 NUM PEAKS: 59
5653 113.03991 15277.0 5653 113.03991 15277.0
5654 123.02419 689099.0 5654 123.02419 689099.0
5655 123.03554 68936.0 5655 123.03554 68936.0
5656 128.04956 14564.0 5656 128.04956 14564.0
5657 129.01041 14843.0 5657 129.01041 14843.0
5658 133.0451 22041.0 5658 133.0451 22041.0
5659 138.99483 1332636.0 5659 138.99483 1332636.0
5660 139.00581 94456.0 5660 139.00581 94456.0
5661 140.02657 19300.0 5661 140.02657 19300.0
5662 146.06032 14189.0 5662 146.06032 14189.0
5663 148.05606 39683.0 5663 148.05606 39683.0
5664 149.01559 14981.0 5664 149.01559 14981.0
5665 155.06064 19858.0 5665 155.06064 19858.0
5666 156.06824 55221.0 5666 156.06824 55221.0
5667 157.07619 36997.0 5667 157.07619 36997.0
5668 164.0265 18608.0 5668 164.0265 18608.0
5669 175.06673 21221.0 5669 175.06673 21221.0
5670 176.05058 19072.0 5670 176.05058 19072.0
5671 177.06996 49682.0 5671 177.06996 49682.0
5672 183.0555 30209.0 5672 183.0555 30209.0
5673 183.06081 88118.0 5673 183.06081 88118.0
5674 184.06332 19768.0 5674 184.06332 19768.0
5675 184.06868 59202.0 5675 184.06868 59202.0
5676 196.06854 97299.0 5676 196.06854 97299.0
5677 197.07671 61139.0 5677 197.07671 61139.0
5678 203.0621 35166.0 5678 203.0621 35166.0
5679 204.06998 19803.0 5679 204.06998 19803.0
5680 204.08092 49291.0 5680 204.08092 49291.0
5681 205.06487 29754.0 5681 205.06487 29754.0
5682 207.06059 882384.0 5682 207.06059 882384.0
5683 208.0686 634275.0 5683 208.0686 634275.0
5684 209.07669 25592.0 5684 209.07669 25592.0
5685 217.0218 165488.0 5685 217.0218 165488.0
5686 219.03754 41019.0 5686 219.03754 41019.0
5687 222.07198 384808.0 5687 222.07198 384808.0
5688 223.03162 30017.0 5688 223.03162 30017.0
5689 223.0799 43854.0 5689 223.0799 43854.0
5690 224.08748 416242.0 5690 224.08748 416242.0
5691 225.07111 247098.0 5691 225.07111 247098.0
5692 225.09467 22048.0 5692 225.09467 22048.0
5693 231.03761 14704.0 5693 231.03761 14704.0
5694 232.07594 99246.0 5694 232.07594 99246.0
5695 234.07179 197210.0 5695 234.07179 197210.0
5696 235.032 192527.0 5696 235.032 192527.0
5697 235.05521 28642.0 5697 235.05521 28642.0
5698 235.07939 264307.0 5698 235.07939 264307.0
5699 236.06332 486776.0 5699 236.06332 486776.0
5700 242.08463 14147.0 5700 242.08463 14147.0
5701 243.03766 1030291.0 5701 243.03766 1030291.0
5702 250.06654 105369.0 5702 250.06654 105369.0
5703 251.07462 143926.0 5703 251.07462 143926.0
5704 251.0981 73184.0 5704 251.0981 73184.0
5705 252.08234 1413294.0 5705 252.08234 1413294.0
5706 260.06421 35847.0 5706 260.06421 35847.0
5707 261.08243 111553.0 5707 261.08243 111553.0
5708 262.0907 121243.0 5708 262.0907 121243.0
5709 263.09796 32958.0 5709 263.09796 32958.0
5710 269.04013 16405.0 5710 269.04013 16405.0
5711 270.04846 16960.0 5711 270.04846 16960.0
5712 5712
5713 COMPOUND_NAME: Paclobutrazol
5713 SCANNUMBER: 1764 5714 SCANNUMBER: 1764
5714 IONMODE: Positive 5715 IONMODE: Positive
5715 SPECTRUMTYPE: Centroid 5716 SPECTRUMTYPE: Centroid
5716 FORMULA: C15H20N3OCl 5717 FORMULA: C15H20N3OCl
5717 INCHIKEY: RMOGWMIKYWRTKW-UONOGXRCSA-N 5718 INCHIKEY: RMOGWMIKYWRTKW-UONOGXRCSA-N
5720 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5721 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5721 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5722 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5722 IONIZATION: ESI+ 5723 IONIZATION: ESI+
5723 LICENSE: CC BY-NC 5724 LICENSE: CC BY-NC
5724 COMMENT: 5725 COMMENT:
5725 COMPOUND_NAME: Paclobutrazol
5726 RETENTION_TIME: 6.358851 5726 RETENTION_TIME: 6.358851
5727 PRECURSOR_MZ: 294.1362 5727 PRECURSOR_MZ: 294.1362
5728 ADDUCT: [M+H]+ 5728 ADDUCT: [M+H]+
5729 COLLISION_ENERGY: 5729 COLLISION_ENERGY:
5730 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5730 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5731 NUM PEAKS: 22 5731 NUM PEAKS: 22
5732 87.0807 394679.0 5732 87.0807 394679.0
5733 89.03882 144548.0 5733 89.03882 144548.0
5734 91.05441 100589.0 5734 91.05441 100589.0
5735 95.04928 72012.0 5735 95.04928 72012.0
5736 102.04659 60868.0 5736 102.04659 60868.0
5737 103.05439 512214.0 5737 103.05439 512214.0
5738 113.0154 191248.0 5738 113.0154 191248.0
5739 115.0543 61507.0 5739 115.0543 61507.0
5740 116.06211 61856.0 5740 116.06211 61856.0
5741 125.01532 6037114.0 5741 125.01532 6037114.0
5742 126.01882 85997.0 5742 126.01882 85997.0
5743 127.01254 4019573.0 5743 127.01254 4019573.0
5744 129.07021 226797.0 5744 129.07021 226797.0
5745 130.078 602958.0 5745 130.078 602958.0
5746 137.01562 331896.0 5746 137.01562 331896.0
5747 139.0309 780894.0 5747 139.0309 780894.0
5748 140.99162 137268.0 5748 140.99162 137268.0
5749 141.00285 65567.0 5749 141.00285 65567.0
5750 141.01048 108664.0 5750 141.01048 108664.0
5751 151.03107 202825.0 5751 151.03107 202825.0
5752 165.04663 986782.0 5752 165.04663 986782.0
5753 173.50876 86407.0 5753 173.50876 86407.0
5754 5754
5755 COMPOUND_NAME: Penconazole
5755 SCANNUMBER: 2459 5756 SCANNUMBER: 2459
5756 IONMODE: Positive 5757 IONMODE: Positive
5757 SPECTRUMTYPE: Centroid 5758 SPECTRUMTYPE: Centroid
5758 FORMULA: C13H15N3Cl2 5759 FORMULA: C13H15N3Cl2
5759 INCHIKEY: WKBPZYKAUNRMKP-JTQLQIEISA-N 5760 INCHIKEY: WKBPZYKAUNRMKP-JTQLQIEISA-N
5762 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5763 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5763 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5764 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5764 IONIZATION: ESI+ 5765 IONIZATION: ESI+
5765 LICENSE: CC BY-NC 5766 LICENSE: CC BY-NC
5766 COMMENT: 5767 COMMENT:
5767 COMPOUND_NAME: Penconazole
5768 RETENTION_TIME: 6.747501 5768 RETENTION_TIME: 6.747501
5769 PRECURSOR_MZ: 284.0724 5769 PRECURSOR_MZ: 284.0724
5770 ADDUCT: [M+H]+ 5770 ADDUCT: [M+H]+
5771 COLLISION_ENERGY: 5771 COLLISION_ENERGY:
5772 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5772 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5773 NUM PEAKS: 5 5773 NUM PEAKS: 5
5774 102.04659 746383.0 5774 102.04659 746383.0
5775 122.99965 1405085.0 5775 122.99965 1405085.0
5776 137.01562 2859486.0 5776 137.01562 2859486.0
5777 158.97626 62049868.0 5777 158.97626 62049868.0
5778 172.99223 3885430.0 5778 172.99223 3885430.0
5779 5779
5780 COMPOUND_NAME: Propiconazole
5780 SCANNUMBER: 3131 5781 SCANNUMBER: 3131
5781 IONMODE: Positive 5782 IONMODE: Positive
5782 SPECTRUMTYPE: Centroid 5783 SPECTRUMTYPE: Centroid
5783 FORMULA: C15H17N3O2Cl2 5784 FORMULA: C15H17N3O2Cl2
5784 INCHIKEY: STJLVHWMYQXCPB-UHFFFAOYSA-N 5785 INCHIKEY: STJLVHWMYQXCPB-UHFFFAOYSA-N
5787 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5788 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5788 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5789 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5789 IONIZATION: ESI+ 5790 IONIZATION: ESI+
5790 LICENSE: CC BY-NC 5791 LICENSE: CC BY-NC
5791 COMMENT: 5792 COMMENT:
5792 COMPOUND_NAME: Propiconazole
5793 RETENTION_TIME: 6.999194 5793 RETENTION_TIME: 6.999194
5794 PRECURSOR_MZ: 342.0777 5794 PRECURSOR_MZ: 342.0777
5795 ADDUCT: [M+H]+ 5795 ADDUCT: [M+H]+
5796 COLLISION_ENERGY: 5796 COLLISION_ENERGY:
5797 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5797 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5798 NUM PEAKS: 5 5798 NUM PEAKS: 5
5799 122.99965 303053.0 5799 122.99965 303053.0
5800 158.97626 24240670.0 5800 158.97626 24240670.0
5801 172.9556 1323126.0 5801 172.9556 1323126.0
5802 186.97108 391981.0 5802 186.97108 391981.0
5803 190.96622 431621.0 5803 190.96622 431621.0
5804 5804
5805 COMPOUND_NAME: Tebuconazole
5805 SCANNUMBER: 2993 5806 SCANNUMBER: 2993
5806 IONMODE: Positive 5807 IONMODE: Positive
5807 SPECTRUMTYPE: Centroid 5808 SPECTRUMTYPE: Centroid
5808 FORMULA: C16H22N3OCl 5809 FORMULA: C16H22N3OCl
5809 INCHIKEY: PXMNMQRDXWABCY-INIZCTEOSA-N 5810 INCHIKEY: PXMNMQRDXWABCY-INIZCTEOSA-N
5812 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5813 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5813 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5814 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5814 IONIZATION: ESI+ 5815 IONIZATION: ESI+
5815 LICENSE: CC BY-NC 5816 LICENSE: CC BY-NC
5816 COMMENT: 5817 COMMENT:
5817 COMPOUND_NAME: Tebuconazole
5818 RETENTION_TIME: 6.933391 5818 RETENTION_TIME: 6.933391
5819 PRECURSOR_MZ: 308.1532 5819 PRECURSOR_MZ: 308.1532
5820 ADDUCT: [M+H]+ 5820 ADDUCT: [M+H]+
5821 COLLISION_ENERGY: 5821 COLLISION_ENERGY:
5822 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5822 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5823 NUM PEAKS: 15 5823 NUM PEAKS: 15
5824 89.03882 78455.0 5824 89.03882 78455.0
5825 103.05439 150981.0 5825 103.05439 150981.0
5826 115.0543 806550.0 5826 115.0543 806550.0
5827 116.06211 1104744.0 5827 116.06211 1104744.0
5828 125.01532 7312966.0 5828 125.01532 7312966.0
5829 129.07021 192428.0 5829 129.07021 192428.0
5830 130.078 394675.0 5830 130.078 394675.0
5831 133.06488 89665.0 5831 133.06488 89665.0
5832 137.01562 81241.0 5832 137.01562 81241.0
5833 139.0309 552019.0 5833 139.0309 552019.0
5834 143.06068 143813.0 5834 143.06068 143813.0
5835 144.09352 109186.0 5835 144.09352 109186.0
5836 151.03107 2225088.0 5836 151.03107 2225088.0
5837 165.04663 474739.0 5837 165.04663 474739.0
5838 179.0621 93619.0 5838 179.0621 93619.0
5839 5839
5840 COMPOUND_NAME: Tetraconazole
5840 SCANNUMBER: 1845 5841 SCANNUMBER: 1845
5841 IONMODE: Positive 5842 IONMODE: Positive
5842 SPECTRUMTYPE: Centroid 5843 SPECTRUMTYPE: Centroid
5843 FORMULA: C13H11N3OCl2F4 5844 FORMULA: C13H11N3OCl2F4
5844 INCHIKEY: LQDARGUHUSPFNL-QMMMGPOBSA-N 5845 INCHIKEY: LQDARGUHUSPFNL-QMMMGPOBSA-N
5847 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5848 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5848 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5849 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5849 IONIZATION: ESI+ 5850 IONIZATION: ESI+
5850 LICENSE: CC BY-NC 5851 LICENSE: CC BY-NC
5851 COMMENT: 5852 COMMENT:
5852 COMPOUND_NAME: Tetraconazole
5853 RETENTION_TIME: 6.434036 5853 RETENTION_TIME: 6.434036
5854 PRECURSOR_MZ: 372.0302 5854 PRECURSOR_MZ: 372.0302
5855 ADDUCT: [M+H]+ 5855 ADDUCT: [M+H]+
5856 COLLISION_ENERGY: 5856 COLLISION_ENERGY:
5857 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5857 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5858 NUM PEAKS: 6 5858 NUM PEAKS: 6
5859 115.05463 210733.0 5859 115.05463 210733.0
5860 149.01559 493803.0 5860 149.01559 493803.0
5861 150.02344 1143618.0 5861 150.02344 1143618.0
5862 158.97679 15780315.0 5862 158.97679 15780315.0
5863 176.96693 301907.0 5863 176.96693 301907.0
5864 184.99236 249943.0 5864 184.99236 249943.0
5865 5865
5866 COMPOUND_NAME: Triflumizole
5866 SCANNUMBER: 2640 5867 SCANNUMBER: 2640
5867 IONMODE: Positive 5868 IONMODE: Positive
5868 SPECTRUMTYPE: Centroid 5869 SPECTRUMTYPE: Centroid
5869 FORMULA: C15H15N3OClF3 5870 FORMULA: C15H15N3OClF3
5870 INCHIKEY: HSMVPDGQOIQYSR-UHFFFAOYSA-N 5871 INCHIKEY: HSMVPDGQOIQYSR-UHFFFAOYSA-N
5873 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5874 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5874 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5875 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5875 IONIZATION: ESI+ 5876 IONIZATION: ESI+
5876 LICENSE: CC BY-NC 5877 LICENSE: CC BY-NC
5877 COMMENT: 5878 COMMENT:
5878 COMPOUND_NAME: Triflumizole
5879 RETENTION_TIME: 6.821252 5879 RETENTION_TIME: 6.821252
5880 PRECURSOR_MZ: 346.094 5880 PRECURSOR_MZ: 346.094
5881 ADDUCT: [M+H]+ 5881 ADDUCT: [M+H]+
5882 COLLISION_ENERGY: 5882 COLLISION_ENERGY:
5883 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5883 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5884 NUM PEAKS: 2 5884 NUM PEAKS: 2
5885 278.05542 29552484.0 5885 278.05542 29552484.0
5886 346.09351 955540.0 5886 346.09351 955540.0
5887 5887
5888 COMPOUND_NAME: Triticonazole
5888 SCANNUMBER: 2549 5889 SCANNUMBER: 2549
5889 IONMODE: Positive 5890 IONMODE: Positive
5890 SPECTRUMTYPE: Centroid 5891 SPECTRUMTYPE: Centroid
5891 FORMULA: C17H20N3OCl 5892 FORMULA: C17H20N3OCl
5892 INCHIKEY: PPDBOQMNKNNODG-QGZVFWFLSA-N 5893 INCHIKEY: PPDBOQMNKNNODG-QGZVFWFLSA-N
5895 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5896 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5896 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5897 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5897 IONIZATION: ESI+ 5898 IONIZATION: ESI+
5898 LICENSE: CC BY-NC 5899 LICENSE: CC BY-NC
5899 COMMENT: 5900 COMMENT:
5900 COMPOUND_NAME: Triticonazole
5901 RETENTION_TIME: 6.793731 5901 RETENTION_TIME: 6.793731
5902 PRECURSOR_MZ: 318.1369 5902 PRECURSOR_MZ: 318.1369
5903 ADDUCT: [M+H]+ 5903 ADDUCT: [M+H]+
5904 COLLISION_ENERGY: 5904 COLLISION_ENERGY:
5905 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5905 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5906 NUM PEAKS: 59 5906 NUM PEAKS: 59
5907 89.03882 57349.0 5907 89.03882 57349.0
5908 91.05464 43853.0 5908 91.05464 43853.0
5909 95.04953 68354.0 5909 95.04953 68354.0
5910 95.08585 78735.0 5910 95.08585 78735.0
5911 105.04505 52373.0 5911 105.04505 52373.0
5912 105.07019 44975.0 5912 105.07019 44975.0
5913 109.06509 75668.0 5913 109.06509 75668.0
5914 109.10148 51915.0 5914 109.10148 51915.0
5915 113.01572 53023.0 5915 113.01572 53023.0
5916 115.05463 68376.0 5916 115.05463 68376.0
5917 123.0806 45319.0 5917 123.0806 45319.0
5918 124.08866 67815.0 5918 124.08866 67815.0
5919 125.0157 4347652.0 5919 125.0157 4347652.0
5920 127.01254 310325.0 5920 127.01254 310325.0
5921 128.06239 303332.0 5921 128.06239 303332.0
5922 130.078 46406.0 5922 130.078 46406.0
5923 138.99483 44710.0 5923 138.99483 44710.0
5924 139.03134 105057.0 5924 139.03134 105057.0
5925 141.0033 76537.0 5925 141.0033 76537.0
5926 141.01048 71845.0 5926 141.01048 71845.0
5927 141.07028 162099.0 5927 141.07028 162099.0
5928 142.07797 64263.0 5928 142.07797 64263.0
5929 145.0649 84426.0 5929 145.0649 84426.0
5930 149.01559 164192.0 5930 149.01559 164192.0
5931 150.97079 108504.0 5931 150.97079 108504.0
5932 151.01263 78052.0 5932 151.01263 78052.0
5933 151.03107 81877.0 5933 151.03107 81877.0
5934 152.0202 168874.0 5934 152.0202 168874.0
5935 152.06247 59642.0 5935 152.06247 59642.0
5936 153.06992 138585.0 5936 153.06992 138585.0
5937 154.07816 168480.0 5937 154.07816 168480.0
5938 155.00728 52088.0 5938 155.00728 52088.0
5939 155.06064 174636.0 5939 155.06064 174636.0
5940 155.07307 63253.0 5940 155.07307 63253.0
5941 155.08603 105852.0 5941 155.08603 105852.0
5942 156.09389 497246.0 5942 156.09389 497246.0
5943 160.97346 52002.0 5943 160.97346 52002.0
5944 161.97681 59631.0 5944 161.97681 59631.0
5945 162.0233 93274.0 5945 162.0233 93274.0
5946 162.97058 1449389.0 5946 162.97058 1449389.0
5947 163.0309 743940.0 5947 163.0309 743940.0
5948 165.04663 51233.0 5948 165.04663 51233.0
5949 165.06996 567265.0 5949 165.06996 567265.0
5950 166.07343 191274.0 5950 166.07343 191274.0
5951 167.0768 126513.0 5951 167.0768 126513.0
5952 167.08606 45824.0 5952 167.08606 45824.0
5953 174.97041 93433.0 5953 174.97041 93433.0
5954 175.0313 553302.0 5954 175.0313 553302.0
5955 176.03931 76155.0 5955 176.03931 76155.0
5956 177.04655 73758.0 5956 177.04655 73758.0
5957 178.96568 128779.0 5957 178.96568 128779.0
5958 181.10179 157033.0 5958 181.10179 157033.0
5959 185.07611 76498.0 5959 185.07611 76498.0
5960 188.98663 142622.0 5960 188.98663 142622.0
5961 189.04662 686868.0 5961 189.04662 686868.0
5962 189.05568 66741.0 5962 189.05568 66741.0
5963 190.04179 48399.0 5963 190.04179 48399.0
5964 191.06258 581232.0 5964 191.06258 581232.0
5965 196.12456 74697.0 5965 196.12456 74697.0
5966 5966
5967 COMPOUND_NAME: Spinetoram L
5967 SCANNUMBER: 3229 5968 SCANNUMBER: 3229
5968 IONMODE: Positive 5969 IONMODE: Positive
5969 SPECTRUMTYPE: Centroid 5970 SPECTRUMTYPE: Centroid
5970 FORMULA: C43H69NO10 5971 FORMULA: C43H69NO10
5971 INCHIKEY: KWVYSEWJJXXTEZ-GDMNSMANSA-N 5972 INCHIKEY: KWVYSEWJJXXTEZ-GDMNSMANSA-N
5974 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 5975 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
5975 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 5976 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
5976 IONIZATION: ESI+ 5977 IONIZATION: ESI+
5977 LICENSE: CC BY-NC 5978 LICENSE: CC BY-NC
5978 COMMENT: 5979 COMMENT:
5979 COMPOUND_NAME: Spinetoram L
5980 RETENTION_TIME: 6.970665 5980 RETENTION_TIME: 6.970665
5981 PRECURSOR_MZ: 760.5021 5981 PRECURSOR_MZ: 760.5021
5982 ADDUCT: [M+H]+ 5982 ADDUCT: [M+H]+
5983 COLLISION_ENERGY: 5983 COLLISION_ENERGY:
5984 INSTRUMENT_TYPE: LC-ESI-Orbitrap 5984 INSTRUMENT_TYPE: LC-ESI-Orbitrap
5985 NUM PEAKS: 21 5985 NUM PEAKS: 21
5986 85.06505 76410.0 5986 85.06505 76410.0
5987 87.04429 159491.0 5987 87.04429 159491.0
5988 95.04928 101292.0 5988 95.04928 101292.0
5989 97.06514 990457.0 5989 97.06514 990457.0
5990 98.09655 3217928.0 5990 98.09655 3217928.0
5991 99.04415 293676.0 5991 99.04415 293676.0
5992 99.08067 604833.0 5992 99.08067 604833.0
5993 101.06004 88798.0 5993 101.06004 88798.0
5994 111.04435 94328.0 5994 111.04435 94328.0
5995 115.0755 369305.0 5995 115.0755 369305.0
5996 124.11241 164399.0 5996 124.11241 164399.0
5997 125.05997 306356.0 5997 125.05997 306356.0
5998 127.07556 185334.0 5998 127.07556 185334.0
5999 142.12299 6861919.0 5999 142.12299 6861919.0
6000 157.08623 113064.0 6000 157.08623 113064.0
6001 160.13321 150610.0 6001 160.13321 150610.0
6002 169.10155 133452.0 6002 169.10155 133452.0
6003 173.50752 93996.0 6003 173.50752 93996.0
6004 183.11732 117521.0 6004 183.11732 117521.0
6005 211.11166 121662.0 6005 211.11166 121662.0
6006 213.09132 89441.0 6006 213.09132 89441.0
6007 6007
6008 COMPOUND_NAME: Emamectin benzoate
6008 SCANNUMBER: 3373 6009 SCANNUMBER: 3373
6009 IONMODE: Positive 6010 IONMODE: Positive
6010 SPECTRUMTYPE: Centroid 6011 SPECTRUMTYPE: Centroid
6011 FORMULA: C49H75NO13 6012 FORMULA: C49H75NO13
6012 INCHIKEY: GCKZANITAMOIAR-XWVCPFKXSA-N 6013 INCHIKEY: GCKZANITAMOIAR-XWVCPFKXSA-N
6015 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6016 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6016 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6017 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6017 IONIZATION: ESI+ 6018 IONIZATION: ESI+
6018 LICENSE: CC BY-NC 6019 LICENSE: CC BY-NC
6019 COMMENT: 6020 COMMENT:
6020 COMPOUND_NAME: Emamectin benzoate
6021 RETENTION_TIME: 6.999389 6021 RETENTION_TIME: 6.999389
6022 PRECURSOR_MZ: 886.5328 6022 PRECURSOR_MZ: 886.5328
6023 ADDUCT: [M+H]+ 6023 ADDUCT: [M+H]+
6024 COLLISION_ENERGY: 6024 COLLISION_ENERGY:
6025 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6025 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6026 NUM PEAKS: 11 6026 NUM PEAKS: 11
6027 95.04928 292923.0 6027 95.04928 292923.0
6028 98.06031 268499.0 6028 98.06031 268499.0
6029 108.08107 688810.0 6029 108.08107 688810.0
6030 109.10148 229513.0 6030 109.10148 229513.0
6031 114.0916 233366.0 6031 114.0916 233366.0
6032 119.08569 201386.0 6032 119.08569 201386.0
6033 123.11689 375128.0 6033 123.11689 375128.0
6034 126.09174 1876739.0 6034 126.09174 1876739.0
6035 140.10709 213152.0 6035 140.10709 213152.0
6036 158.11794 18414448.0 6036 158.11794 18414448.0
6037 173.50876 230972.0 6037 173.50876 230972.0
6038 6038
6039 COMPOUND_NAME: Fenpropimorph
6039 SCANNUMBER: 1283 6040 SCANNUMBER: 1283
6040 IONMODE: Positive 6041 IONMODE: Positive
6041 SPECTRUMTYPE: Centroid 6042 SPECTRUMTYPE: Centroid
6042 FORMULA: C20H33NO 6043 FORMULA: C20H33NO
6043 INCHIKEY: RYAUSSKQMZRMAI-ALOPSCKCSA-N 6044 INCHIKEY: RYAUSSKQMZRMAI-ALOPSCKCSA-N
6046 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6047 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6047 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6048 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6048 IONIZATION: ESI+ 6049 IONIZATION: ESI+
6049 LICENSE: CC BY-NC 6050 LICENSE: CC BY-NC
6050 COMMENT: 6051 COMMENT:
6051 COMPOUND_NAME: Fenpropimorph
6052 RETENTION_TIME: 4.613603 6052 RETENTION_TIME: 4.613603
6053 PRECURSOR_MZ: 304.2642 6053 PRECURSOR_MZ: 304.2642
6054 ADDUCT: [M+H]+ 6054 ADDUCT: [M+H]+
6055 COLLISION_ENERGY: 6055 COLLISION_ENERGY:
6056 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6056 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6057 NUM PEAKS: 14 6057 NUM PEAKS: 14
6058 91.05441 1025363.0 6058 91.05441 1025363.0
6059 98.09655 5764430.0 6059 98.09655 5764430.0
6060 102.09142 427096.0 6060 102.09142 427096.0
6061 105.0699 3838997.0 6061 105.0699 3838997.0
6062 107.08563 608609.0 6062 107.08563 608609.0
6063 116.10709 2962134.0 6063 116.10709 2962134.0
6064 117.06997 1187727.0 6064 117.06997 1187727.0
6065 119.08569 5923314.0 6065 119.08569 5923314.0
6066 130.1226 4460902.0 6066 130.1226 4460902.0
6067 132.09351 5501752.0 6067 132.09351 5501752.0
6068 145.10147 350602.0 6068 145.10147 350602.0
6069 147.11678 29169826.0 6069 147.11678 29169826.0
6070 161.13254 881881.0 6070 161.13254 881881.0
6071 304.26379 2555976.0 6071 304.26379 2555976.0
6072 6072
6073 COMPOUND_NAME: Spirodiclofen
6073 SCANNUMBER: 4501 6074 SCANNUMBER: 4501
6074 IONMODE: Positive 6075 IONMODE: Positive
6075 SPECTRUMTYPE: Centroid 6076 SPECTRUMTYPE: Centroid
6076 FORMULA: C21H24O4Cl2 6077 FORMULA: C21H24O4Cl2
6077 INCHIKEY: DTDSAWVUFPGDMX-UHFFFAOYSA-N 6078 INCHIKEY: DTDSAWVUFPGDMX-UHFFFAOYSA-N
6080 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6081 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6081 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6082 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6082 IONIZATION: ESI+ 6083 IONIZATION: ESI+
6083 LICENSE: CC BY-NC 6084 LICENSE: CC BY-NC
6084 COMMENT: 6085 COMMENT:
6085 COMPOUND_NAME: Spirodiclofen
6086 RETENTION_TIME: 7.279784 6086 RETENTION_TIME: 7.279784
6087 PRECURSOR_MZ: 411.1127 6087 PRECURSOR_MZ: 411.1127
6088 ADDUCT: [M+H]+ 6088 ADDUCT: [M+H]+
6089 COLLISION_ENERGY: 6089 COLLISION_ENERGY:
6090 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6090 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6091 NUM PEAKS: 3 6091 NUM PEAKS: 3
6092 313.03357 548684.0 6092 313.03357 548684.0
6093 313.03952 12618725.0 6093 313.03952 12618725.0
6094 411.11246 2380661.0 6094 411.11246 2380661.0
6095 6095
6096 COMPOUND_NAME: Spinosad
6096 SCANNUMBER: 2899 6097 SCANNUMBER: 2899
6097 IONMODE: Positive 6098 IONMODE: Positive
6098 SPECTRUMTYPE: Centroid 6099 SPECTRUMTYPE: Centroid
6099 FORMULA: C41H65NO10 6100 FORMULA: C41H65NO10
6100 INCHIKEY: SRJQTHAZUNRMPR-SFGMUSMWSA-N 6101 INCHIKEY: SRJQTHAZUNRMPR-SFGMUSMWSA-N
6103 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6104 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6104 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6105 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6105 IONIZATION: ESI+ 6106 IONIZATION: ESI+
6106 LICENSE: CC BY-NC 6107 LICENSE: CC BY-NC
6107 COMMENT: 6108 COMMENT:
6108 COMPOUND_NAME: Spinosad
6109 RETENTION_TIME: 6.884336 6109 RETENTION_TIME: 6.884336
6110 PRECURSOR_MZ: 732.4695 6110 PRECURSOR_MZ: 732.4695
6111 ADDUCT: [M+H]+ 6111 ADDUCT: [M+H]+
6112 COLLISION_ENERGY: 6112 COLLISION_ENERGY:
6113 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6113 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6114 NUM PEAKS: 24 6114 NUM PEAKS: 24
6115 85.06505 290872.0 6115 85.06505 290872.0
6116 95.08585 281431.0 6116 95.08585 281431.0
6117 97.06514 4107321.0 6117 97.06514 4107321.0
6118 98.09655 11811636.0 6118 98.09655 11811636.0
6119 99.04415 1980639.0 6119 99.04415 1980639.0
6120 99.08067 1702591.0 6120 99.08067 1702591.0
6121 101.05976 1777858.0 6121 101.05976 1777858.0
6122 113.05991 355791.0 6122 113.05991 355791.0
6123 115.0755 428942.0 6123 115.0755 428942.0
6124 124.11241 549097.0 6124 124.11241 549097.0
6125 125.05997 1372437.0 6125 125.05997 1372437.0
6126 129.09106 504378.0 6126 129.09106 504378.0
6127 142.12299 24420248.0 6127 142.12299 24420248.0
6128 145.08598 799808.0 6128 145.08598 799808.0
6129 155.08551 1085827.0 6129 155.08551 1085827.0
6130 157.08623 650576.0 6130 157.08623 650576.0
6131 160.13321 457492.0 6131 160.13321 457492.0
6132 169.10155 538427.0 6132 169.10155 538427.0
6133 173.50937 310025.0 6133 173.50937 310025.0
6134 183.08075 246373.0 6134 183.08075 246373.0
6135 197.09599 753984.0 6135 197.09599 753984.0
6136 199.07574 416158.0 6136 199.07574 416158.0
6137 201.0916 354498.0 6137 201.0916 354498.0
6138 225.09103 339682.0 6138 225.09103 339682.0
6139 6139
6140 COMPOUND_NAME: Spirotetramat
6140 SCANNUMBER: 1978 6141 SCANNUMBER: 1978
6141 IONMODE: Positive 6142 IONMODE: Positive
6142 SPECTRUMTYPE: Centroid 6143 SPECTRUMTYPE: Centroid
6143 FORMULA: C21H27NO5 6144 FORMULA: C21H27NO5
6144 INCHIKEY: CLSVJBIHYWPGQY-UHFFFAOYSA-N 6145 INCHIKEY: CLSVJBIHYWPGQY-UHFFFAOYSA-N
6147 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6148 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6148 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6149 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6149 IONIZATION: ESI+ 6150 IONIZATION: ESI+
6150 LICENSE: CC BY-NC 6151 LICENSE: CC BY-NC
6151 COMMENT: 6152 COMMENT:
6152 COMPOUND_NAME: Spirotetramat
6153 RETENTION_TIME: 6.637813 6153 RETENTION_TIME: 6.637813
6154 PRECURSOR_MZ: 374.1972 6154 PRECURSOR_MZ: 374.1972
6155 ADDUCT: [M+H]+ 6155 ADDUCT: [M+H]+
6156 COLLISION_ENERGY: 6156 COLLISION_ENERGY:
6157 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6157 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6158 NUM PEAKS: 25 6158 NUM PEAKS: 25
6159 117.07031 3145654.0 6159 117.07031 3145654.0
6160 119.08569 1788706.0 6160 119.08569 1788706.0
6161 131.08598 559926.0 6161 131.08598 559926.0
6162 143.08594 1443391.0 6162 143.08594 1443391.0
6163 145.06535 755443.0 6163 145.06535 755443.0
6164 145.10147 3741174.0 6164 145.10147 3741174.0
6165 147.08087 660014.0 6165 147.08087 660014.0
6166 155.08603 1939864.0 6166 155.08603 1939864.0
6167 157.10155 488130.0 6167 157.10155 488130.0
6168 160.11253 518572.0 6168 160.11253 518572.0
6169 169.10155 615151.0 6169 169.10155 615151.0
6170 173.06003 2045691.0 6170 173.06003 2045691.0
6171 173.09608 1047769.0 6171 173.09608 1047769.0
6172 182.10933 614118.0 6172 182.10933 614118.0
6173 183.11732 922964.0 6173 183.11732 922964.0
6174 188.10699 1101991.0 6174 188.10699 1101991.0
6175 192.09375 469162.0 6175 192.09375 469162.0
6176 197.13313 1231311.0 6176 197.13313 1231311.0
6177 207.11739 667038.0 6177 207.11739 667038.0
6178 216.10236 45921764.0 6178 216.10236 45921764.0
6179 225.12729 615992.0 6179 225.12729 615992.0
6180 244.13345 5845476.0 6180 244.13345 5845476.0
6181 253.12317 483222.0 6181 253.12317 483222.0
6182 270.14972 5260680.0 6182 270.14972 5260680.0
6183 302.17508 467268.0 6183 302.17508 467268.0
6184 6184
6185 COMPOUND_NAME: Spinetoram J
6185 SCANNUMBER: 2785 6186 SCANNUMBER: 2785
6186 IONMODE: Positive 6187 IONMODE: Positive
6187 SPECTRUMTYPE: Centroid 6188 SPECTRUMTYPE: Centroid
6188 FORMULA: C42H69NO10 6189 FORMULA: C42H69NO10
6189 INCHIKEY: GOENIMGKWNZVDA-RWGFPKGXSA-N 6190 INCHIKEY: GOENIMGKWNZVDA-RWGFPKGXSA-N
6192 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6193 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6193 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6194 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6194 IONIZATION: ESI+ 6195 IONIZATION: ESI+
6195 LICENSE: CC BY-NC 6196 LICENSE: CC BY-NC
6196 COMMENT: 6197 COMMENT:
6197 COMPOUND_NAME: Spinetoram J
6198 RETENTION_TIME: 6.875065 6198 RETENTION_TIME: 6.875065
6199 PRECURSOR_MZ: 748.4996 6199 PRECURSOR_MZ: 748.4996
6200 ADDUCT: [M+H]+ 6200 ADDUCT: [M+H]+
6201 COLLISION_ENERGY: 6201 COLLISION_ENERGY:
6202 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6202 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6203 NUM PEAKS: 19 6203 NUM PEAKS: 19
6204 87.04429 367892.0 6204 87.04429 367892.0
6205 95.04928 288081.0 6205 95.04928 288081.0
6206 97.06488 2777411.0 6206 97.06488 2777411.0
6207 98.09655 8992013.0 6207 98.09655 8992013.0
6208 99.04415 801171.0 6208 99.04415 801171.0
6209 99.08067 1598443.0 6209 99.08067 1598443.0
6210 111.04435 203657.0 6210 111.04435 203657.0
6211 115.0755 975367.0 6211 115.0755 975367.0
6212 124.11241 446241.0 6212 124.11241 446241.0
6213 125.05997 894301.0 6213 125.05997 894301.0
6214 127.07556 507677.0 6214 127.07556 507677.0
6215 142.12299 18851726.0 6215 142.12299 18851726.0
6216 157.08623 430463.0 6216 157.08623 430463.0
6217 157.10155 1058798.0 6217 157.10155 1058798.0
6218 160.13321 524113.0 6218 160.13321 524113.0
6219 171.11707 230127.0 6219 171.11707 230127.0
6220 199.11194 246050.0 6220 199.11194 246050.0
6221 203.10715 581698.0 6221 203.10715 581698.0
6222 217.12222 236328.0 6222 217.12222 236328.0
6223 6223
6224 COMPOUND_NAME: Hydramethylnon
6224 SCANNUMBER: 1646 6225 SCANNUMBER: 1646
6225 IONMODE: Positive 6226 IONMODE: Positive
6226 SPECTRUMTYPE: Centroid 6227 SPECTRUMTYPE: Centroid
6227 FORMULA: C25H24N4F6 6228 FORMULA: C25H24N4F6
6228 INCHIKEY: IQVNEKKDSLOHHK-UHFFFAOYSA-N 6229 INCHIKEY: IQVNEKKDSLOHHK-UHFFFAOYSA-N
6231 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6232 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6232 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6233 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6233 IONIZATION: ESI+ 6234 IONIZATION: ESI+
6234 LICENSE: CC BY-NC 6235 LICENSE: CC BY-NC
6235 COMMENT: 6236 COMMENT:
6236 COMPOUND_NAME: Hydramethylnon
6237 RETENTION_TIME: 6.67979 6237 RETENTION_TIME: 6.67979
6238 PRECURSOR_MZ: 495.1986 6238 PRECURSOR_MZ: 495.1986
6239 ADDUCT: [M+H]+ 6239 ADDUCT: [M+H]+
6240 COLLISION_ENERGY: 6240 COLLISION_ENERGY:
6241 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6241 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6242 NUM PEAKS: 48 6242 NUM PEAKS: 48
6243 86.09703 592073.0 6243 86.09703 592073.0
6244 97.07668 1102254.0 6244 97.07668 1102254.0
6245 102.04713 162761.0 6245 102.04713 162761.0
6246 109.07671 152336.0 6246 109.07671 152336.0
6247 111.09241 210434.0 6247 111.09241 210434.0
6248 112.08799 1438576.0 6248 112.08799 1438576.0
6249 112.1001 1334338.0 6249 112.1001 1334338.0
6250 113.10799 1043525.0 6250 113.10799 1043525.0
6251 126.10352 2018271.0 6251 126.10352 2018271.0
6252 127.11132 687935.0 6252 127.11132 687935.0
6253 128.1188 2868988.0 6253 128.1188 2868988.0
6254 151.03604 3123530.0 6254 151.03604 3123530.0
6255 153.11414 318101.0 6255 153.11414 318101.0
6256 159.04243 1900688.0 6256 159.04243 1900688.0
6257 163.12367 266550.0 6257 163.12367 266550.0
6258 169.04726 264978.0 6258 169.04726 264978.0
6259 171.04259 9972201.0 6259 171.04259 9972201.0
6260 178.04718 949330.0 6260 178.04718 949330.0
6261 183.04219 978938.0 6261 183.04219 978938.0
6262 196.0376 218268.0 6262 196.0376 218268.0
6263 198.05374 693364.0 6263 198.05374 693364.0
6264 209.05803 231723.0 6264 209.05803 231723.0
6265 213.06461 1076938.0 6265 213.06461 1076938.0
6266 214.04874 274804.0 6266 214.04874 274804.0
6267 218.05339 138241.0 6267 218.05339 138241.0
6268 223.04858 173264.0 6268 223.04858 173264.0
6269 225.06474 1428863.0 6269 225.06474 1428863.0
6270 238.05968 4320120.0 6270 238.05968 4320120.0
6271 239.08025 155000.0 6271 239.08025 155000.0
6272 247.08057 319312.0 6272 247.08057 319312.0
6273 253.14586 318558.0 6273 253.14586 318558.0
6274 255.08643 272181.0 6274 255.08643 272181.0
6275 267.08603 1563035.0 6275 267.08603 1563035.0
6276 270.13541 250539.0 6276 270.13541 250539.0
6277 281.12677 392614.0 6277 281.12677 392614.0
6278 295.14307 440522.0 6278 295.14307 440522.0
6279 298.08517 500719.0 6279 298.08517 500719.0
6280 298.15424 170519.0 6280 298.15424 170519.0
6281 299.09323 317366.0 6281 299.09323 317366.0
6282 307.14276 192450.0 6282 307.14276 192450.0
6283 323.14941 13337730.0 6283 323.14941 13337730.0
6284 328.07541 186287.0 6284 328.07541 186287.0
6285 334.15344 701456.0 6285 334.15344 701456.0
6286 348.08228 404641.0 6286 348.08228 404641.0
6287 353.0658 262110.0 6287 353.0658 262110.0
6288 366.07346 193709.0 6288 366.07346 193709.0
6289 368.08932 5815862.0 6289 368.08932 5815862.0
6290 495.20059 2433116.0 6290 495.20059 2433116.0
6291 6291
6292 COMPOUND_NAME: Aminocarb_1
6292 SCANNUMBER: 742 6293 SCANNUMBER: 742
6293 IONMODE: Positive 6294 IONMODE: Positive
6294 SPECTRUMTYPE: Centroid 6295 SPECTRUMTYPE: Centroid
6295 FORMULA: C11H16N2O2 6296 FORMULA: C11H16N2O2
6296 INCHIKEY: IMIDOCRTMDIQIJ-UHFFFAOYSA-N 6297 INCHIKEY: IMIDOCRTMDIQIJ-UHFFFAOYSA-N
6299 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6300 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6300 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6301 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6301 IONIZATION: ESI+ 6302 IONIZATION: ESI+
6302 LICENSE: CC BY-NC 6303 LICENSE: CC BY-NC
6303 COMMENT: 6304 COMMENT:
6304 COMPOUND_NAME: Aminocarb_1
6305 RETENTION_TIME: 0.8035756 6305 RETENTION_TIME: 0.8035756
6306 PRECURSOR_MZ: 209.129 6306 PRECURSOR_MZ: 209.129
6307 ADDUCT: [M+H]+ 6307 ADDUCT: [M+H]+
6308 COLLISION_ENERGY: 6308 COLLISION_ENERGY:
6309 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6309 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6310 NUM PEAKS: 5 6310 NUM PEAKS: 5
6311 120.05733 176701.0 6311 120.05733 176701.0
6312 122.06016 1917070.0 6312 122.06016 1917070.0
6313 136.07611 928093.0 6313 136.07611 928093.0
6314 137.08363 8823033.0 6314 137.08363 8823033.0
6315 152.10725 186336.0 6315 152.10725 186336.0
6316 6316
6317 COMPOUND_NAME: Aminocarb_2
6317 SCANNUMBER: 1198 6318 SCANNUMBER: 1198
6318 IONMODE: Positive 6319 IONMODE: Positive
6319 SPECTRUMTYPE: Centroid 6320 SPECTRUMTYPE: Centroid
6320 FORMULA: C11H16N2O2 6321 FORMULA: C11H16N2O2
6321 INCHIKEY: IMIDOCRTMDIQIJ-UHFFFAOYSA-N 6322 INCHIKEY: IMIDOCRTMDIQIJ-UHFFFAOYSA-N
6324 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6325 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6325 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6326 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6326 IONIZATION: ESI+ 6327 IONIZATION: ESI+
6327 LICENSE: CC BY-NC 6328 LICENSE: CC BY-NC
6328 COMMENT: 6329 COMMENT:
6329 COMPOUND_NAME: Aminocarb_2
6330 RETENTION_TIME: 1.13997 6330 RETENTION_TIME: 1.13997
6331 PRECURSOR_MZ: 209.129 6331 PRECURSOR_MZ: 209.129
6332 ADDUCT: [M+H]+ 6332 ADDUCT: [M+H]+
6333 COLLISION_ENERGY: 6333 COLLISION_ENERGY:
6334 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6334 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6335 NUM PEAKS: 5 6335 NUM PEAKS: 5
6336 120.05733 247123.0 6336 120.05733 247123.0
6337 122.06016 2666029.0 6337 122.06016 2666029.0
6338 136.07611 1253139.0 6338 136.07611 1253139.0
6339 137.08363 12201258.0 6339 137.08363 12201258.0
6340 152.10725 242082.0 6340 152.10725 242082.0
6341 6341
6342 COMPOUND_NAME: Propamocarb_1
6342 SCANNUMBER: 687 6343 SCANNUMBER: 687
6343 IONMODE: Positive 6344 IONMODE: Positive
6344 SPECTRUMTYPE: Centroid 6345 SPECTRUMTYPE: Centroid
6345 FORMULA: C9H20N2O2 6346 FORMULA: C9H20N2O2
6346 INCHIKEY: WZZLDXDUQPOXNW-UHFFFAOYSA-N 6347 INCHIKEY: WZZLDXDUQPOXNW-UHFFFAOYSA-N
6349 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6350 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6350 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6351 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6351 IONIZATION: ESI+ 6352 IONIZATION: ESI+
6352 LICENSE: CC BY-NC 6353 LICENSE: CC BY-NC
6353 COMMENT: 6354 COMMENT:
6354 COMPOUND_NAME: Propamocarb_1
6355 RETENTION_TIME: 0.7535679 6355 RETENTION_TIME: 0.7535679
6356 PRECURSOR_MZ: 189.1603 6356 PRECURSOR_MZ: 189.1603
6357 ADDUCT: [M+H]+ 6357 ADDUCT: [M+H]+
6358 COLLISION_ENERGY: 6358 COLLISION_ENERGY:
6359 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6359 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6360 NUM PEAKS: 2 6360 NUM PEAKS: 2
6361 86.0966 201548.0 6361 86.0966 201548.0
6362 102.05516 5038638.0 6362 102.05516 5038638.0
6363 6363
6364 COMPOUND_NAME: Propamocarb_2
6364 SCANNUMBER: 1108 6365 SCANNUMBER: 1108
6365 IONMODE: Positive 6366 IONMODE: Positive
6366 SPECTRUMTYPE: Centroid 6367 SPECTRUMTYPE: Centroid
6367 FORMULA: C9H20N2O2 6368 FORMULA: C9H20N2O2
6368 INCHIKEY: WZZLDXDUQPOXNW-UHFFFAOYSA-N 6369 INCHIKEY: WZZLDXDUQPOXNW-UHFFFAOYSA-N
6371 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6372 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6372 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6373 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6373 IONIZATION: ESI+ 6374 IONIZATION: ESI+
6374 LICENSE: CC BY-NC 6375 LICENSE: CC BY-NC
6375 COMMENT: 6376 COMMENT:
6376 COMPOUND_NAME: Propamocarb_2
6377 RETENTION_TIME: 1.081971 6377 RETENTION_TIME: 1.081971
6378 PRECURSOR_MZ: 189.1603 6378 PRECURSOR_MZ: 189.1603
6379 ADDUCT: [M+H]+ 6379 ADDUCT: [M+H]+
6380 COLLISION_ENERGY: 6380 COLLISION_ENERGY:
6381 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6381 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6382 NUM PEAKS: 2 6382 NUM PEAKS: 2
6383 86.0966 107829.0 6383 86.0966 107829.0
6384 102.05516 2507023.0 6384 102.05516 2507023.0
6385 6385
6386 COMPOUND_NAME: Formetanate_1
6386 SCANNUMBER: 711 6387 SCANNUMBER: 711
6387 IONMODE: Positive 6388 IONMODE: Positive
6388 SPECTRUMTYPE: Centroid 6389 SPECTRUMTYPE: Centroid
6389 FORMULA: C11H15N3O2 6390 FORMULA: C11H15N3O2
6390 INCHIKEY: MYPKGPZHHQEODQ-UHFFFAOYSA-N 6391 INCHIKEY: MYPKGPZHHQEODQ-UHFFFAOYSA-N
6393 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6394 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6394 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6395 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6395 IONIZATION: ESI+ 6396 IONIZATION: ESI+
6396 LICENSE: CC BY-NC 6397 LICENSE: CC BY-NC
6397 COMMENT: 6398 COMMENT:
6398 COMPOUND_NAME: Formetanate_1
6399 RETENTION_TIME: 0.7730471 6399 RETENTION_TIME: 0.7730471
6400 PRECURSOR_MZ: 222.1239 6400 PRECURSOR_MZ: 222.1239
6401 ADDUCT: [M+H]+ 6401 ADDUCT: [M+H]+
6402 COLLISION_ENERGY: 6402 COLLISION_ENERGY:
6403 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6403 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6404 NUM PEAKS: 13 6404 NUM PEAKS: 13
6405 93.03365 1796.0 6405 93.03365 1796.0
6406 107.04935 1981.0 6406 107.04935 1981.0
6407 111.04435 82262.0 6407 111.04435 82262.0
6408 118.04142 1927.0 6408 118.04142 1927.0
6409 120.04462 150907.0 6409 120.04462 150907.0
6410 121.03984 67610.0 6410 121.03984 67610.0
6411 122.06016 5909.0 6411 122.06016 5909.0
6412 122.75254 1678.0 6412 122.75254 1678.0
6413 150.98424 1930.0 6413 150.98424 1930.0
6414 165.1024 143887.0 6414 165.1024 143887.0
6415 173.50876 2616.0 6415 173.50876 2616.0
6416 200.05632 2056.0 6416 200.05632 2056.0
6417 208.52768 2170.0 6417 208.52768 2170.0
6418 6418
6419 COMPOUND_NAME: Formetanate_2
6419 SCANNUMBER: 1161 6420 SCANNUMBER: 1161
6420 IONMODE: Positive 6421 IONMODE: Positive
6421 SPECTRUMTYPE: Centroid 6422 SPECTRUMTYPE: Centroid
6422 FORMULA: C11H15N3O2 6423 FORMULA: C11H15N3O2
6423 INCHIKEY: MYPKGPZHHQEODQ-UHFFFAOYSA-N 6424 INCHIKEY: MYPKGPZHHQEODQ-UHFFFAOYSA-N
6426 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6427 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6427 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6428 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6428 IONIZATION: ESI+ 6429 IONIZATION: ESI+
6429 LICENSE: CC BY-NC 6430 LICENSE: CC BY-NC
6430 COMMENT: 6431 COMMENT:
6431 COMPOUND_NAME: Formetanate_2
6432 RETENTION_TIME: 1.13043 6432 RETENTION_TIME: 1.13043
6433 PRECURSOR_MZ: 222.1239 6433 PRECURSOR_MZ: 222.1239
6434 ADDUCT: [M+H]+ 6434 ADDUCT: [M+H]+
6435 COLLISION_ENERGY: 6435 COLLISION_ENERGY:
6436 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6436 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6437 NUM PEAKS: 15 6437 NUM PEAKS: 15
6438 91.05441 6330.0 6438 91.05441 6330.0
6439 93.03365 27201.0 6439 93.03365 27201.0
6440 107.04935 4024.0 6440 107.04935 4024.0
6441 111.04435 131558.0 6441 111.04435 131558.0
6442 115.05429 3711.0 6442 115.05429 3711.0
6443 117.06996 5571.0 6443 117.06996 5571.0
6444 118.04177 4476.0 6444 118.04177 4476.0
6445 120.04462 274740.0 6445 120.04462 274740.0
6446 121.03984 113412.0 6446 121.03984 113412.0
6447 122.06016 7843.0 6447 122.06016 7843.0
6448 124.07605 4049.0 6448 124.07605 4049.0
6449 135.04427 4178.0 6449 135.04427 4178.0
6450 145.06488 3067.0 6450 145.06488 3067.0
6451 164.95049 3848.0 6451 164.95049 3848.0
6452 165.1024 263802.0 6452 165.1024 263802.0
6453 6453
6454 COMPOUND_NAME: Mexacarbate
6454 SCANNUMBER: 1328 6455 SCANNUMBER: 1328
6455 IONMODE: Positive 6456 IONMODE: Positive
6456 SPECTRUMTYPE: Centroid 6457 SPECTRUMTYPE: Centroid
6457 FORMULA: C12H18N2O2 6458 FORMULA: C12H18N2O2
6458 INCHIKEY: YNEVBPNZHBAYOA-UHFFFAOYSA-N 6459 INCHIKEY: YNEVBPNZHBAYOA-UHFFFAOYSA-N
6461 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6462 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6462 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6463 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6463 IONIZATION: ESI+ 6464 IONIZATION: ESI+
6464 LICENSE: CC BY-NC 6465 LICENSE: CC BY-NC
6465 COMMENT: 6466 COMMENT:
6466 COMPOUND_NAME: Mexacarbate
6467 RETENTION_TIME: 1.682191 6467 RETENTION_TIME: 1.682191
6468 PRECURSOR_MZ: 223.1443 6468 PRECURSOR_MZ: 223.1443
6469 ADDUCT: [M+H]+ 6469 ADDUCT: [M+H]+
6470 COLLISION_ENERGY: 6470 COLLISION_ENERGY:
6471 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6471 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6472 NUM PEAKS: 5 6472 NUM PEAKS: 5
6473 134.07283 2632951.0 6473 134.07283 2632951.0
6474 136.07611 26036728.0 6474 136.07611 26036728.0
6475 150.092 1572118.0 6475 150.092 1572118.0
6476 151.09932 54847764.0 6476 151.09932 54847764.0
6477 166.12282 1541928.0 6477 166.12282 1541928.0
6478 6478
6479 COMPOUND_NAME: Monceren
6479 SCANNUMBER: 3999 6480 SCANNUMBER: 3999
6480 IONMODE: Positive 6481 IONMODE: Positive
6481 SPECTRUMTYPE: Centroid 6482 SPECTRUMTYPE: Centroid
6482 FORMULA: C19H21N2OCl 6483 FORMULA: C19H21N2OCl
6483 INCHIKEY: OGYFATSSENRIKG-UHFFFAOYSA-N 6484 INCHIKEY: OGYFATSSENRIKG-UHFFFAOYSA-N
6486 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6487 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6487 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6488 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6488 IONIZATION: ESI+ 6489 IONIZATION: ESI+
6489 LICENSE: CC BY-NC 6490 LICENSE: CC BY-NC
6490 COMMENT: 6491 COMMENT:
6491 COMPOUND_NAME: Monceren
6492 RETENTION_TIME: 7.14553 6492 RETENTION_TIME: 7.14553
6493 PRECURSOR_MZ: 329.1426 6493 PRECURSOR_MZ: 329.1426
6494 ADDUCT: [M+H]+ 6494 ADDUCT: [M+H]+
6495 COLLISION_ENERGY: 6495 COLLISION_ENERGY:
6496 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6496 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6497 NUM PEAKS: 5 6497 NUM PEAKS: 5
6498 89.03881 550831.0 6498 89.03881 550831.0
6499 94.06543 635265.0 6499 94.06543 635265.0
6500 106.06545 446416.0 6500 106.06545 446416.0
6501 125.01307 512150.0 6501 125.01307 512150.0
6502 125.01532 37442116.0 6502 125.01532 37442116.0
6503 6503
6504 COMPOUND_NAME: Desmedipham
6504 SCANNUMBER: 2271 6505 SCANNUMBER: 2271
6505 IONMODE: Positive 6506 IONMODE: Positive
6506 SPECTRUMTYPE: Centroid 6507 SPECTRUMTYPE: Centroid
6507 FORMULA: C16H16N2O4 6508 FORMULA: C16H16N2O4
6508 INCHIKEY: WZJZMXBKUWKXTQ-UHFFFAOYSA-N 6509 INCHIKEY: WZJZMXBKUWKXTQ-UHFFFAOYSA-N
6511 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6512 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6512 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6513 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6513 IONIZATION: ESI+ 6514 IONIZATION: ESI+
6514 LICENSE: CC BY-NC 6515 LICENSE: CC BY-NC
6515 COMMENT: 6516 COMMENT:
6516 COMPOUND_NAME: Desmedipham
6517 RETENTION_TIME: 6.430396 6517 RETENTION_TIME: 6.430396
6518 PRECURSOR_MZ: 301.1192 6518 PRECURSOR_MZ: 301.1192
6519 ADDUCT: [M+H]+ 6519 ADDUCT: [M+H]+
6520 COLLISION_ENERGY: 6520 COLLISION_ENERGY:
6521 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6521 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6522 NUM PEAKS: 3 6522 NUM PEAKS: 3
6523 136.03947 1773399.0 6523 136.03947 1773399.0
6524 154.04993 1002798.0 6524 154.04993 1002798.0
6525 182.08162 6480130.0 6525 182.08162 6480130.0
6526 6526
6527 COMPOUND_NAME: Phenmedipham
6527 SCANNUMBER: 2458 6528 SCANNUMBER: 2458
6528 IONMODE: Positive 6529 IONMODE: Positive
6529 SPECTRUMTYPE: Centroid 6530 SPECTRUMTYPE: Centroid
6530 FORMULA: C16H16N2O4 6531 FORMULA: C16H16N2O4
6531 INCHIKEY: IDOWTHOLJBTAFI-UHFFFAOYSA-N 6532 INCHIKEY: IDOWTHOLJBTAFI-UHFFFAOYSA-N
6534 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ) 6535 AUTHORS: Biomarker Analytical Laboratories, RECETOX, Masaryk University (CZ)
6535 INSTRUMENT: LC Orbitrap Fusion Tribrid MS 6536 INSTRUMENT: LC Orbitrap Fusion Tribrid MS
6536 IONIZATION: ESI+ 6537 IONIZATION: ESI+
6537 LICENSE: CC BY-NC 6538 LICENSE: CC BY-NC
6538 COMMENT: 6539 COMMENT:
6539 COMPOUND_NAME: Phenmedipham
6540 RETENTION_TIME: 6.570995 6540 RETENTION_TIME: 6.570995
6541 PRECURSOR_MZ: 301.1185 6541 PRECURSOR_MZ: 301.1185
6542 ADDUCT: [M+H]+ 6542 ADDUCT: [M+H]+
6543 COLLISION_ENERGY: 6543 COLLISION_ENERGY:
6544 INSTRUMENT_TYPE: LC-ESI-Orbitrap 6544 INSTRUMENT_TYPE: LC-ESI-Orbitrap
6545 NUM PEAKS: 2 6545 NUM PEAKS: 2
6546 136.03947 2596929.0 6546 136.03947 2596929.0
6547 168.06587 7038054.0 6547 168.06587 7038054.0
6548 6548