Record Index Results
Search
Contents
Download
Documentation
About MassBank
News Archive
Index Type :
Compound Name:
F
Back to Record Index
Results :
4,577 Hit.
( 928 - 1,072 Displayed )
First
Prev
1
2
3
4
5
6
7
8
9
10
Next
Last
( Total
21
Page )
▼
Results End
Name
Formula / Structure
ExactMass
ID
Fentanyl
20 spectra
C22H28N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
336.22015
LC-ESI-Q; MS; POS; 15 V
MSBNK-Waters-WA001020
LC-ESI-Q; MS; POS; 30 V
MSBNK-Waters-WA001019
LC-ESI-Q; MS; POS; 45 V
MSBNK-Waters-WA001018
LC-ESI-Q; MS; POS; 60 V
MSBNK-Waters-WA001017
LC-ESI-Q; MS; POS; 75 V
MSBNK-Waters-WA001016
LC-ESI-Q; MS; POS; 90 V
MSBNK-Waters-WA001015
LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
MSBNK-Eawag-EQ364007
LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
MSBNK-Eawag-EQ364008
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ364001
LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
MSBNK-Eawag-EQ364009
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ364002
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ364003
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ364004
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ364005
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ364006
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU154501
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU154502
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU154503
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU154504
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU154505
Fenthion
16 spectra
C10H15O3PS2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
278.02002
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA086601AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA086603B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA086605070APH
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA086611C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA086613D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA0866155BE0PH
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0866213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0866237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA086625AF82PH
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
MSBNK-CASMI_2016-SM848001
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315501
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315502
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315503
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315504
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315505
LC-ESI-QTOF; MS2; CE: Ramp 20.8-31.3 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU315506
Fenthion Oxon
9 spectra
C10H15O4PS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
262.04291
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125307
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125301
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125308
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125309
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125302
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125303
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125304
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125305
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125306
Fenthion Oxon Sulfone
9 spectra
C10H15O6PS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
294.03271
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125407
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125401
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125408
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125409
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125402
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125403
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125404
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125405
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01125406
Fenthion-sulfone
9 spectra
C10H15O5PS2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
310.00986
LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
MSBNK-Eawag-EQ359907
LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
MSBNK-Eawag-EQ359908
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ359901
LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
MSBNK-Eawag-EQ359909
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ359902
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ359903
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ359904
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ359905
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ359906
Fenthion-sulfoxide
14 spectra
C10H15O4PS2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
294.01495
LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
MSBNK-Eawag-EQ370707
LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
MSBNK-Eawag-EQ370708
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ370701
LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
MSBNK-Eawag-EQ370709
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ370702
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ370703
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ370704
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ370705
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ370706
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU301401
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU301402
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU301403
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU301404
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU301405
Fenuron
26 spectra
C9H12N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
164.09500
LC-APCI-QFT; MS2; CE: Ramp 20%-70% (nominal); R=30000; [M+H]+
MSBNK-ACES_SU-AS000111
LC-APCI-QFT; MS2; CE: Ramp 20%-70% (nominal); R=30000; [M-H]-
MSBNK-ACES_SU-AS000051
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF404503
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF404501
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF404504
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF404502
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU116301
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ311101
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU116302
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ311102
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
MSBNK-CASMI_2016-SM842501
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU116303
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ311103
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU116304
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ311104
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU116305
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ311105
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU116306
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ311106
LC-ESI-QFT; MS2; CE: Ramp 20%-70% (nominal); R=30000; [M+H]+
MSBNK-ACES_SU-AS000182
LC-ESI-QFT; MS2; CE: Ramp 20%-70% (nominal); R=30000; [M-H]-
MSBNK-ACES_SU-AS000246
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU261101
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU261102
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU261103
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU261104
LC-ESI-QTOF; MS2; CE: Ramp 16.7-25.1 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU261106
Ferimzone E
4 spectra
C15H18N4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
254.15315
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
MSBNK-Waters-WA000125
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
MSBNK-Waters-WA000126
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
MSBNK-Waters-WA000127
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
MSBNK-Waters-WA000128
Ferimzone Z
4 spectra
C15H18N4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
254.15315
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
MSBNK-Waters-WA000129
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
MSBNK-Waters-WA000130
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
MSBNK-Waters-WA000131
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
MSBNK-Waters-WA000132
Ferocaulicin
5 spectra
C26H30O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
438.52539
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+Na]+
MSBNK-RIKEN_NPDepo-NGA00242
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+Na]+
MSBNK-RIKEN_NPDepo-NGA00243
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+Na]+
MSBNK-RIKEN_NPDepo-NGA00244
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+Na]+
MSBNK-RIKEN_NPDepo-NGA00241
LC-ESI-QQQ; MS; [M+H]+
MSBNK-RIKEN_NPDepo-CB000257
FERROCENE
1 spectrum
C12H14Fe
214.04449
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005442
Ferulaldehyde, 4-Hydroxy-3-methoxycinnamaldehyde, ...
5 spectra
C10H10O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
178.18700
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS000601
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS000602
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS000607
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS000608
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS000609
Ferulic acid
4 spectra
C10H10O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
194.05791
GC-EI-TOF; MS; 2 TMS; BP:249
MSBNK-Kazusa-KZ000133
GC-EI-TOF; MS; 2 TMS; BP:323
MSBNK-Kazusa-KZ000089
GC-EI-TOF; MS; n TMS; RT:808.375 sec
MSBNK-Osaka_Univ-OUF00227
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PM000409
Ferulic acid, 4-Hydroxy-3-methoxycinnamic acid, 3-...
3 spectra
C10H10O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
194.18600
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT100110
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT100113
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT200110
Ferulic acid, 4-Hydroxy-3-methoxycinnamic acid, tr...
6 spectra
C10H10O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
194.18600
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS001101
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS001102
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS001103
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS103901
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS103902
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS103907
Feruloyl agmatine (isomer of 1607)
1 spectrum
C15H22N4O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
306.36600
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311014
Feruloyl agmatine (isomer of 1608)
1 spectrum
C15H22N4O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
306.36600
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311015
Feruloyl allylamine
1 spectrum
C13H15NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
233.26700
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311011
Feruloyl dehydrotyramine (isomer of 1654)
1 spectrum
C18H17NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
311.33701
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311018
Feruloyl dehydrotyramine (isomer of 1655)
1 spectrum
C18H17NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
311.33701
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311019
Feruloyl Hexoside (isomer of 847)
1 spectrum
C16H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.32700
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309327
Feruloyl Hexoside (isomer of 849)
1 spectrum
C16H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.32700
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309328
Feruloyl Lactate
1 spectrum
C13H14O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
282.24799
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309326
Feruloyl lysine
1 spectrum
C16H22N2O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
322.36099
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311016
Feruloyl O-methyldehydrodopamine
1 spectrum
C19H19NO5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
341.36301
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311022
First
Prev
1
2
3
4
5
6
7
8
9
10
Next
Last
( Total
21
Page )
▲
Results Top
Imprint
Data Privacy
Feedback
system version 2.2.8
Copyright © 2006 MassBank Project; 2011
NORMAN Association
; 2021
MassBank Consortium