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2,241 Hit.
( 1,465 - 1,587 Displayed )
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Name
Formula / Structure
ExactMass
ID
ORTHO-METHYLPHENETOLE
1 spectrum
C9H12O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
136.08882
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004023
ORTHO-METHYLPHENOL
1 spectrum
C7H8O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
108.05751
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004014
ORTHO-NITROBENZOIC ACID
1 spectrum
C7H5NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
167.02187
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009414
ORTHO-NITROPHENOL
1 spectrum
C6H5NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
139.02695
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP000227
ORTHO-PHENETIDINE
1 spectrum
C8H11NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
137.08406
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005864
ORTHO-PHENYLENEDIAMINE
2 spectra
C6H8N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
108.06875
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001297
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010792
ORTHO-PHTHALIC ACID BIS(TRIMETHYLSILYL) ESTER
1 spectrum
C14H22O4Si2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
310.10565
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP000597
ORTHO-SEC-BUTYLPHENOL
1 spectrum
C10H14O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.10448
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004063
ORTHO-TERPHENYL
1 spectrum
C18H14
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
230.10954
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP012362
ORTHO-TERT-BUTYLPHENOL
1 spectrum
C10H14O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.10448
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004062
ORTHO-TOLUENESULFONAMIDE
1 spectrum
C7H9NO2S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
171.03540
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010795
ORTHO-TOLUIDINE
2 spectra
C7H9N
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
107.07350
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001334
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003983
ORTHO-TOLUNITRILE
1 spectrum
C8H7N
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
117.05785
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001649
ORTHO-TOLYL ACETATE
2 spectra
C9H10O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.06808
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005977
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005913
ORTHO-TOLYL BENZOATE
1 spectrum
C14H12O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
212.08372
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP007587
ORTHO-TOLYLACETIC ACID
1 spectrum
C9H10O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.06808
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010378
ORTHO-VANILLIN
1 spectrum
C8H8O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
152.04733
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009420
ORTHO-XYLENE
2 spectra
C8H10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
106.07825
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP012246
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001533
Ortophosphate
6 spectra
H3O4P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
97.97690
LC-ESI-QTOF; MS2; CE: 10; R=; [M+H]+
MSBNK-BGC_Munich-RP022401
LC-ESI-QTOF; MS2; CE: 10; R=; [M-H]-
MSBNK-BGC_Munich-RP022411
LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
MSBNK-BGC_Munich-RP022402
LC-ESI-QTOF; MS2; CE: 20; R=; [M-H]-
MSBNK-BGC_Munich-RP022412
LC-ESI-QTOF; MS2; CE: 40; R=; [M+H]+
MSBNK-BGC_Munich-RP022403
LC-ESI-QTOF; MS2; CE: 40; R=; [M-H]-
MSBNK-BGC_Munich-RP022413
Oryzalin
36 spectra
C12H18N4O6S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
346.09470
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ309901
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
MSBNK-Eawag-EQ309951
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ309902
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
MSBNK-Eawag-EQ309952
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
MSBNK-CASMI_2016-SM846503
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M-H]-
MSBNK-CASMI_2016-SM846552
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ309903
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
MSBNK-Eawag-EQ309953
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ309904
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
MSBNK-Eawag-EQ309954
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ309905
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
MSBNK-Eawag-EQ309955
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ309906
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
MSBNK-Eawag-EQ309956
LC-ESI-QQ; MS2; CE:10 V; [M-H]-
MSBNK-Waters-WA000037
LC-ESI-QQ; MS2; CE:20 V; [M-H]-
MSBNK-Waters-WA000038
LC-ESI-QQ; MS2; CE:30 V; [M-H]-
MSBNK-Waters-WA000039
LC-ESI-QQ; MS2; CE:40 V; [M-H]-
MSBNK-Waters-WA000040
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M-H]-
MSBNK-Athens_Univ-AU233357
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M-H]-
MSBNK-Athens_Univ-AU233358
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M-H]-
MSBNK-Athens_Univ-AU233359
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M-H]-
MSBNK-Athens_Univ-AU233360
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 10 V
MSBNK-MSSJ-MSJ02239
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 20 V
MSBNK-MSSJ-MSJ02240
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 30 V
MSBNK-MSSJ-MSJ02241
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 40 V
MSBNK-MSSJ-MSJ02242
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 50 V
MSBNK-MSSJ-MSJ02243
LC-ESI-QTOF; MS2; ESI; NEGATIVE; [M-H]-; CE 60 V
MSBNK-MSSJ-MSJ02244
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 10 V
MSBNK-MSSJ-MSJ02232
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 20 V
MSBNK-MSSJ-MSJ02233
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 30 V
MSBNK-MSSJ-MSJ02234
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 40 V
MSBNK-MSSJ-MSJ02235
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 50 V
MSBNK-MSSJ-MSJ02236
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 60 V
MSBNK-MSSJ-MSJ02237
LC-ESI-QTOF; MS; ESI; NEGATIVE
MSBNK-MSSJ-MSJ02238
LC-ESI-QTOF; MS; ESI; POSITIVE
MSBNK-MSSJ-MSJ02231
osajin
5 spectra
C25H24O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
404.46701
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02923
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02922
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02921
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02924
LC-ESI-QQQ; MS; [M+H]+
MSBNK-RIKEN_NPDepo-CB000308
osas#9
6 spectra
C23H33NO10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
483.21039
LC-ESI-QTOF; MS2; CE: 10; R=; [M+H]+
MSBNK-BGC_Munich-RP009401
LC-ESI-QTOF; MS2; CE: 10; R=; [M-H]-
MSBNK-BGC_Munich-RP009411
LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
MSBNK-BGC_Munich-RP009402
LC-ESI-QTOF; MS2; CE: 20; R=; [M-H]-
MSBNK-BGC_Munich-RP009412
LC-ESI-QTOF; MS2; CE: 40; R=; [M+H]+
MSBNK-BGC_Munich-RP009403
LC-ESI-QTOF; MS2; CE: 40; R=; [M-H]-
MSBNK-BGC_Munich-RP009413
Oscillamide Y
9 spectra
C45H59N7O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
857.43231
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ436007
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ436001
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ436008
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ436009
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ436002
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ436003
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ436004
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ436005
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ436006
Oscillaxanthin
1 spectrum
C52H76O12
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
892.53369
FAB-EBEB; MS2; m/z: 892.53; [M]+*
MSBNK-Kyoto_Univ-CA000090
Oseltamivir
38 spectra
C16H28N2O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
312.20490
LC-APPI-QQ; MS
MSBNK-PFOS_research_group-FFF00285
LC-APPI-QQ; MS2; CE10; [M+H]+
MSBNK-PFOS_research_group-FFF00284
LC-APPI-QQ; MS2; CE20; [M+H]+
MSBNK-PFOS_research_group-FFF00283
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA065808
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA065802
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA065809
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA065803
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA065814
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA065801
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA065810
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA065804
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA065811
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-Eawag-EA065805
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-Eawag-EA065812
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA065806
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
MSBNK-Eawag-EA065813
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
MSBNK-Eawag-EA065807
LC-ESI-QTOF; MS2; 10 V
MSBNK-BAFG-CSL2311096336
LC-ESI-QTOF; MS2; 100 V
MSBNK-BAFG-CSL2311096342
LC-ESI-QTOF; MS2; 110 V
MSBNK-BAFG-CSL2311096339
LC-ESI-QTOF; MS2; 120 V
MSBNK-BAFG-CSL2311096331
LC-ESI-QTOF; MS2; 130 V
MSBNK-BAFG-CSL2311096332
LC-ESI-QTOF; MS2; 140 V
MSBNK-BAFG-CSL2311096334
LC-ESI-QTOF; MS2; 150 V
MSBNK-BAFG-CSL2311096346
LC-ESI-QTOF; MS2; 20 V
MSBNK-BAFG-CSL2311096344
LC-ESI-QTOF; MS2; 30 V
MSBNK-BAFG-CSL2311096345
LC-ESI-QTOF; MS2; 40 V
MSBNK-BAFG-CSL2311096335
LC-ESI-QTOF; MS2; 40 V
MSBNK-BAFG-CSL2311096338
LC-ESI-QTOF; MS2; 50 V
MSBNK-BAFG-CSL2311096333
LC-ESI-QTOF; MS2; 60 V
MSBNK-BAFG-CSL2311096337
LC-ESI-QTOF; MS2; 70 V
MSBNK-BAFG-CSL2311096340
LC-ESI-QTOF; MS2; 80 V
MSBNK-BAFG-CSL2311096343
LC-ESI-QTOF; MS2; 90 V
MSBNK-BAFG-CSL2311096341
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU206801
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU206802
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU206803
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU206804
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU206805
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