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LC-ESI-ITFT
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20,038 Hit.
( 12,971 - 13,268 Displayed )
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( Total
71
Page )
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Results End
Name
Formula / Structure
ExactMass
ID
Nonaethylene glycol
32 spectra
C18H38O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
414.24649
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+Na]+
MSBNK-UFZ-UP000385
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+Na]+
MSBNK-UFZ-UP000521
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+Na]+
MSBNK-UFZ-UP000533
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+Na]+
MSBNK-UFZ-UP000535
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+Na]+
MSBNK-UFZ-UP000386
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+Na]+
MSBNK-UFZ-UP000429
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+Na]+
MSBNK-UFZ-UP000387
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+Na]+
MSBNK-UFZ-UP000430
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+Na]+
MSBNK-UFZ-UP000388
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+Na]+
MSBNK-UFZ-UP000431
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+Na]+
MSBNK-UFZ-UP000389
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+Na]+
MSBNK-UFZ-UP000432
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+Na]+
MSBNK-UFZ-UP000433
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+Na]+
MSBNK-UFZ-UP000465
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+Na]+
MSBNK-UFZ-UP000464
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+Na]+
MSBNK-UFZ-UP000483
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+Na]+
MSBNK-UFZ-UP000467
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+Na]+
MSBNK-UFZ-UP000482
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+Na]+
MSBNK-UFZ-UP000466
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+Na]+
MSBNK-UFZ-UP000485
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+Na]+
MSBNK-UFZ-UP000484
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+Na]+
MSBNK-UFZ-UP000498
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+Na]+
MSBNK-UFZ-UP000468
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+Na]+
MSBNK-UFZ-UP000510
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+Na]+
MSBNK-UFZ-UP000500
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+Na]+
MSBNK-UFZ-UP000511
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+Na]+
MSBNK-UFZ-UP000509
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+Na]+
MSBNK-UFZ-UP000522
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+Na]+
MSBNK-UFZ-UP000499
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+Na]+
MSBNK-UFZ-UP000534
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+Na]+
MSBNK-UFZ-UP000523
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+Na]+
MSBNK-UFZ-UP000536
Norethindrone
3 spectra
C20H26O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
298.19327
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA022011C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA022013D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA0220155BE0PH
Norethisterone / norethindrone
4 spectra
C20H26O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
298.19330
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF415003
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF415001
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF415004
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF415002
Norfloxacin
23 spectra
C16H18FN3O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
319.13321
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA060301AD6CPH
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA023208
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA023202
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA060303B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA023209
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA060305070APH
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA023203
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA023214
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA023201
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA060311C9CFPH
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA023210
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA023204
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA060313D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA023211
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA0603155BE0PH
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA023205
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0603213166PH
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA023212
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA023206
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0603237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA060325AF82PH
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA023213
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA023207
Norgestimate
9 spectra
C23H31NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
369.23041
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA022201AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA022203B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA022205070APH
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA022211C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA022213D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA0222155BE0PH
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0222213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0222237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA022225AF82PH
Norgestrel
6 spectra
C21H28O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
312.20892
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA221301AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA221303B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA221305070APH
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA221311C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA221313D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA2213155BE0PH
Norlichexanthone
12 spectra
C14H10O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
258.05280
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003611
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003099
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003612
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003101
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003613
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003103
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004071
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003100
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004072
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003102
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004073
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003104
NP1EC (TENTATIVE)
1 spectrum
C17H26O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
278.18820
LC-ESI-ITFT; MS2; HCD60; [M-H]-
MSBNK-Eawag_Additional_Specs-ETS00010
NT 2 Toxin
6 spectra
C17H24O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
340.15219
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002958
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002960
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002962
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002959
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002961
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002963
Nylidrin
76 spectra
C19H25NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
299.18851
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000201
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002394
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000231
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000247
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000236
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000244
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000233
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000249
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000238
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000252
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000235
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000257
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000240
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000254
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000241
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000259
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000246
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000243
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000248
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000202
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000206
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002395
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000245
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000250
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000251
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000256
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000253
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000258
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000255
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000260
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000203
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000207
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002396
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000208
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002397
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000205
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000209
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002398
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000204
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000210
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000212
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002399
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000211
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000217
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002400
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000214
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000216
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002401
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002402
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000213
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000219
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002403
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000218
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000222
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002404
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000215
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000227
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002405
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000220
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000224
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002406
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000221
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000229
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002407
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000226
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000232
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002408
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000223
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000237
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002409
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000228
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000234
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000225
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000239
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000230
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB000242
o-Anisic acid
5 spectra
C8H8O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
152.04733
LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000079
LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000080
LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000081
LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000082
LC-ESI-ITFT; MS; [M+H]+; isotope pattern
MSBNK-MPI_for_Chemical_Ecology-CE000083
O-desmethylvenlafaxine
14 spectra
C16H25NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
263.18851
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA105308
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA105302
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA105309
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA105303
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA105314
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA105301
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA105310
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA105304
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA105311
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA105305
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA105312
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA105306
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA105313
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA105307
o-Dianisidine
4 spectra
C14H16N2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
244.12120
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF414003
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF414001
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF414004
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF414002
o-phenetidine
4 spectra
C8H11NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
137.08411
LC-ESI-ITFT; MS2; CE: 35 eV; R=30000; [M+H]+
MSBNK-KWR-KW104303
LC-ESI-ITFT; MS2; CE: 35 eV; R=7500; [M+H]+
MSBNK-KWR-KW104302
LC-ESI-ITFT; MS2; CE: 35 eV; R=nominal; [M+H]+
MSBNK-KWR-KW104301
LC-ESI-ITFT; MS2; CE: 65 eV; R=30000; [M+H]+
MSBNK-KWR-KW104304
o-Toluidine
9 spectra
C7H9N
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
107.07350
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA064901AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA064903B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA064905070APH
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA064911C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA064913D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA0649155BE0PH
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0649213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0649237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA064925AF82PH
Ochratoxin A
10 spectra
C20H18ClNO6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
403.08224
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000204
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+Na]+
MSBNK-AAFC-AC000209
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000205
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+Na]+
MSBNK-AAFC-AC000210
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000206
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+Na]+
MSBNK-AAFC-AC000211
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+H]+
MSBNK-AAFC-AC000207
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+Na]+
MSBNK-AAFC-AC000212
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+
MSBNK-AAFC-AC000208
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+Na]+
MSBNK-AAFC-AC000213
Ochratoxin B
17 spectra
C20H19NO6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
369.12122
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000791
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003508
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002947
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003509
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002949
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000792
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003510
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002951
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000793
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003996
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002948
LC-ESI-ITFT; MS2; CE: 40; R=17500; [M+H]+
MSBNK-AAFC-AC000794
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003997
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002950
LC-ESI-ITFT; MS2; CE: 55; R=17500; [M+H]+
MSBNK-AAFC-AC000795
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003998
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002952
Ochratoxin B ethyl ester
5 spectra
C22H23NO6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
397.15253
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000796
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000797
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000798
LC-ESI-ITFT; MS2; CE: 40; R=17500; [M+H]+
MSBNK-AAFC-AC000799
LC-ESI-ITFT; MS2; CE: 55; R=17500; [M+H]+
MSBNK-AAFC-AC000800
Octaethylene glycol
24 spectra
C16H34O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
370.22031
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+Na]+
MSBNK-UFZ-UP000390
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+Na]+
MSBNK-UFZ-UP000391
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+Na]+
MSBNK-UFZ-UP000434
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+Na]+
MSBNK-UFZ-UP000392
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+Na]+
MSBNK-UFZ-UP000435
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+Na]+
MSBNK-UFZ-UP000393
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+Na]+
MSBNK-UFZ-UP000436
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+Na]+
MSBNK-UFZ-UP000394
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+Na]+
MSBNK-UFZ-UP000437
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+Na]+
MSBNK-UFZ-UP000438
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+Na]+
MSBNK-UFZ-UP000470
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+Na]+
MSBNK-UFZ-UP000469
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+Na]+
MSBNK-UFZ-UP000487
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+Na]+
MSBNK-UFZ-UP000472
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+Na]+
MSBNK-UFZ-UP000486
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+Na]+
MSBNK-UFZ-UP000471
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+Na]+
MSBNK-UFZ-UP000489
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+Na]+
MSBNK-UFZ-UP000488
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+Na]+
MSBNK-UFZ-UP000512
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+Na]+
MSBNK-UFZ-UP000513
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+Na]+
MSBNK-UFZ-UP000524
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+Na]+
MSBNK-UFZ-UP000537
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+Na]+
MSBNK-UFZ-UP000525
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+Na]+
MSBNK-UFZ-UP000538
Octyl-methoxycinnamate
2 spectra
C18H26O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
290.18820
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA019401AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA019403B085PH
Ofloxacin
7 spectra
C18H20FN3O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
361.14380
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF407503
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF407501
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF407504
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF407502
LC-ESI-ITFT; MS; Positive
MSBNK-MSSJ-MSJ00032
LC-ESI-ITFT; MS; Positive; CE 20 V
MSBNK-MSSJ-MSJ00030
LC-ESI-ITFT; MS; Positive; CE 40 V
MSBNK-MSSJ-MSJ00031
Oleandrin
4 spectra
C32H48O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
576.32977
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-NaToxAq-NA002307
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-NaToxAq-NA002308
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-NaToxAq-NA002702
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-NaToxAq-NA002703
Ondansetron
6 spectra
C18H19N3O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
293.15280
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA215911C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA215913D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA2159155BE0PH
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA2159213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA2159237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA215925AF82PH
OP (TENTATIVE)
1 spectrum
C14H22O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
206.16710
LC-ESI-ITFT; MS2; HCD75; [M+H]+
MSBNK-Eawag_Additional_Specs-ETS00011
Orbencarb
14 spectra
C12H16ClNOS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
257.06470
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA006908
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA006902
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA006909
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA006903
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA006914
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA006901
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA006910
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA006904
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA006911
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA006905
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA006912
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA006906
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA006913
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA006907
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NORMAN Association
; 2021
MassBank Consortium
Responsible:
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