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LC-ESI-ITFT
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Results :
20,038 Hit.
( 13,543 - 13,811 Displayed )
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( Total
71
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Results End
Name
Formula / Structure
ExactMass
ID
Perfluorohexanoic acid
8 spectra
C6HF11O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
313.98010
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA271558
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA271552
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA271559
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA271553
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA271551
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA271554
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-Eawag-EA271555
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA271557
Perfluorononanoic acid
8 spectra
C9HF17O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
463.97049
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA271858
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA271852
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA271859
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA271853
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA271851
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA271854
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M-H]-
MSBNK-Eawag-EA271856
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA271857
Perfluorooctane sulfonamidoacetic acid
8 spectra
C10H4F17NO4S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
556.95898
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA291958
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA291959
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA291951
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA291960
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA291954
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
MSBNK-Eawag-EA291961
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-Eawag-EA291955
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M-H]-
MSBNK-Eawag-EA291962
Perfluorooctanoic acid
8 spectra
C8HF15O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
413.97369
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA271758
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA271752
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA271759
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA271753
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA271751
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA271760
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA271754
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA271757
Perfluorooctyl phosphate
22 spectra
C8H6F13O4P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
443.97961
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA292408
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA292458
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA292402
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA292452
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA292409
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA292459
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA292403
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA292453
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA292451
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA292410
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA292460
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA292404
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA292454
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA292411
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
MSBNK-Eawag-EA292461
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA292405
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA292412
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M-H]-
MSBNK-Eawag-EA292462
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA292406
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M-H]-
MSBNK-Eawag-EA292456
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-Eawag-EA292413
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA292407
Perfluoropentanoic acid
6 spectra
C5HF9O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
263.98331
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA271458
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA271452
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA271459
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA271451
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA271460
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA271457
Perfluoroundecanoic acid
2 spectra
C11HF21O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
563.96411
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA272252
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA272251
Pethoxamid
7 spectra
C16H22ClNO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
295.13391
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA014401AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA014403B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA014405070APH
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF406203
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF406201
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF406204
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF406202
Pethoxamide
14 spectra
C16H22ClNO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
295.13339
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA070008
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA070002
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA070009
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA070003
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA070014
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA070001
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA070010
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA070004
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA070011
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA070005
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA070012
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA070006
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA070013
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA070007
Phacidin
5 spectra
C16H22O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
294.14673
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000695
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000696
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000697
LC-ESI-ITFT; MS2; CE: 40; R=17500; [M+H]+
MSBNK-AAFC-AC000698
LC-ESI-ITFT; MS2; CE: 55; R=17500; [M+H]+
MSBNK-AAFC-AC000699
Phantolide
6 spectra
C17H24O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
244.18271
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA023401AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA023403B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA023405070APH
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0234213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0234237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA023425AF82PH
Phenazone
14 spectra
C11H12N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
188.09500
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002410
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002411
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002412
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002413
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002414
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002415
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002416
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002417
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0003213166PH
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002418
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002419
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0003237762PH
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002420
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA000325AF82PH
Phenazone / antipyrine
6 spectra
C11H12N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
188.09500
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF406803
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+Na]+
MSBNK-UFZ-UF406835
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF406801
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF406804
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+Na]+
MSBNK-UFZ-UF406836
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF406802
Phenmedipham
14 spectra
C16H16N2O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
300.11160
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA009408
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA009402
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA009409
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA009403
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA009414
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA009401
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA009410
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA009404
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA009411
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA009405
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA009412
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA009406
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA009413
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA009407
Phentermine
76 spectra
C10H15N
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
149.12041
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001401
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002421
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001431
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001447
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001436
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001444
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001433
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001449
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001438
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001452
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001435
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001457
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001440
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001454
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001441
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001459
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001446
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001443
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001448
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001402
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001406
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002422
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001445
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001450
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001451
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001456
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001453
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001458
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001455
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001460
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001403
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001407
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002423
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001408
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002424
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001405
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001409
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002425
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001404
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001410
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001412
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002426
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001411
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001417
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002427
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001414
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001416
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002428
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002429
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001413
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001419
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002430
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001418
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001422
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002431
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001415
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001427
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002432
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001420
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001424
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002433
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001421
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001429
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002434
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001426
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001432
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002435
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001423
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001437
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002436
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001428
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001434
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001425
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001439
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001430
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001442
Phenylalanine
14 spectra
C9H11NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
165.07898
LC-ESI-ITFT; MS2; CE 10.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000285
LC-ESI-ITFT; MS2; CE 15.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000277
LC-ESI-ITFT; MS2; CE 20.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000281
LC-ESI-ITFT; MS2; CE 25.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000278
LC-ESI-ITFT; MS2; CE 30.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000282
LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000036
LC-ESI-ITFT; MS2; CE 35.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000280
LC-ESI-ITFT; MS2; CE 40.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000284
LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000037
LC-ESI-ITFT; MS2; CE 45.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000283
LC-ESI-ITFT; MS2; CE 5.0 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000279
LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000038
LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000039
LC-ESI-ITFT; MS; [M+H]+; isotope pattern
MSBNK-MPI_for_Chemical_Ecology-CE000040
Phenylbenzimidazole sulfonic acid
4 spectra
C13H10N2O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
274.04120
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M-H]-
MSBNK-UFZ-UF417253
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M-H]-
MSBNK-UFZ-UF417251
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M-H]-
MSBNK-UFZ-UF417254
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M-H]-
MSBNK-UFZ-UF417252
Phlorizin
5 spectra
C21H24O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
436.13696
LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000071
LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000072
LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000073
LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000074
LC-ESI-ITFT; MS; [M+H]+; isotope pattern
MSBNK-MPI_for_Chemical_Ecology-CE000075
Phosphatidylcholine 12:0-16:0 / 14:0-14:0
2 spectra
C72H144N2O16P2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1354.99915
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.79; Exp: 1
MSBNK-Chubu_Univ-UT001279
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 12.79; Exp: 1
MSBNK-Chubu_Univ-UT001644
Phosphatidylcholine 14:0-16:0
9 spectra
C38H76NO8P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
705.53082
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 19.51; Exp: 1
MSBNK-Chubu_Univ-UT001280
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 19.51; Exp: 2
MSBNK-Chubu_Univ-UT002021
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 19.51; Exp: 3
MSBNK-Chubu_Univ-UT002749
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 19.53; Exp: 1
MSBNK-Chubu_Univ-UT001000
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 19.53; Exp: 2
MSBNK-Chubu_Univ-UT001735
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 19.51; Exp: 1
MSBNK-Chubu_Univ-UT001645
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 19.51; Exp: 3
MSBNK-Chubu_Univ-UT003107
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 19.53; Exp: 1
MSBNK-Chubu_Univ-UT001518
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 19.53; Exp: 2
MSBNK-Chubu_Univ-UT002257
Phosphatidylcholine 14:0-18:2
6 spectra
C40H76NO8P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
729.53082
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 13.43; Exp: 1
MSBNK-Chubu_Univ-UT001001
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 13.43; Exp: 2
MSBNK-Chubu_Univ-UT001736
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 13.43; Exp: 3
MSBNK-Chubu_Univ-UT002472
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.43; Exp: 1
MSBNK-Chubu_Univ-UT001519
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.43; Exp: 2
MSBNK-Chubu_Univ-UT002258
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.43; Exp: 3
MSBNK-Chubu_Univ-UT002982
Phosphatidylcholine 14:0-18:2 / 16:1-16:1
3 spectra
C80H152N2O16P2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1459.06177
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.46; Exp: 1
MSBNK-Chubu_Univ-UT001646
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.46; Exp: 2
MSBNK-Chubu_Univ-UT002390
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 13.46; Exp: 3
MSBNK-Chubu_Univ-UT003108
Phosphatidylcholine 14:0-20:3
6 spectra
C42H78NO8P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
755.54651
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 14.49; Exp: 1
MSBNK-Chubu_Univ-UT001002
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 14.49; Exp: 2
MSBNK-Chubu_Univ-UT001737
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 14.49; Exp: 3
MSBNK-Chubu_Univ-UT002473
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 14.49; Exp: 1
MSBNK-Chubu_Univ-UT001520
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 14.49; Exp: 2
MSBNK-Chubu_Univ-UT002259
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 14.49; Exp: 3
MSBNK-Chubu_Univ-UT002983
Phosphatidylcholine 14:0-20:4
10 spectra
C42H76NO8P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
753.53082
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.29; Exp: 1
MSBNK-Chubu_Univ-UT001003
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.29; Exp: 2
MSBNK-Chubu_Univ-UT001738
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.29; Exp: 3
MSBNK-Chubu_Univ-UT002474
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.34; Exp: 1
MSBNK-Chubu_Univ-UT001282
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.34; Exp: 2
MSBNK-Chubu_Univ-UT002023
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 12.34; Exp: 3
MSBNK-Chubu_Univ-UT002751
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 12.29; Exp: 1
MSBNK-Chubu_Univ-UT001521
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 12.29; Exp: 2
MSBNK-Chubu_Univ-UT002260
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 12.29; Exp: 3
MSBNK-Chubu_Univ-UT002984
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 12.34; Exp: 1
MSBNK-Chubu_Univ-UT001647
Phosphatidylcholine 14:0-20:5
6 spectra
C42H74NO8P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
751.51520
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 9.43; Exp: 1
MSBNK-Chubu_Univ-UT001004
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 9.43; Exp: 2
MSBNK-Chubu_Univ-UT001739
LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 9.43; Exp: 3
MSBNK-Chubu_Univ-UT002475
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 9.43; Exp: 1
MSBNK-Chubu_Univ-UT001522
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 9.43; Exp: 2
MSBNK-Chubu_Univ-UT002261
LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 9.43; Exp: 3
MSBNK-Chubu_Univ-UT002985
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