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84,026 Hit.
( 67,197 - 67,371 Displayed )
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Results End
Name
Formula / Structure
ExactMass
ID
Phentermine
121 spectra
C10H15N
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
149.12041
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002739
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002740
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002741
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002742
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002743
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002744
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002745
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002746
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002748
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002747
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
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002201
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002009
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002202
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002203
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002010
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002204
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002205
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002206
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002207
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002011
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002208
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002209
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002210
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002211
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002212
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002213
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002214
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002215
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002012
LC-ESI-QFT; MS2; CE: CE15; R=17500; [M+H]+
MSBNK-HBM4EU-HB002791
LC-ESI-QFT; MS2; CE: CE30; R=17500; [M+H]+
MSBNK-HBM4EU-HB002792
LC-ESI-QFT; MS2; CE: CE45; R=17500; [M+H]+
MSBNK-HBM4EU-HB002793
LC-ESI-QFT; MS2; CE: CE60; R=17500; [M+H]+
MSBNK-HBM4EU-HB002794
LC-ESI-QFT; MS2; CE: CE75; R=17500; [M+H]+
MSBNK-HBM4EU-HB002795
LC-ESI-QFT; MS2; CE: CE90; R=17500; [M+H]+
MSBNK-HBM4EU-HB002796
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002590
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002591
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002592
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002593
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002594
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002595
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002596
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002597
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002599
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002598
Phenthoate
9 spectra
C12H17O4PS2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
320.03061
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129207
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129201
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129208
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129209
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129202
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129203
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129204
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129205
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01129206
PHENYL 2-PYRIDYL KETONE
1 spectrum
C12H9NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
183.06841
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP007862
PHENYL 3-PYRIDYL KETONE
1 spectrum
C12H9NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
183.06841
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP007863
PHENYL ACETATE
5 spectra
C8H8O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
136.05243
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005960
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001532
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004944
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005897
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP006896
PHENYL ACETIC ACID ETHYL ESTER
1 spectrum
C10H12O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
164.08372
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP002139
PHENYL BENZOATE
2 spectra
C13H10O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
198.06808
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001513
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008494
PHENYL BUTYRATE
1 spectrum
C10H12O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
164.08372
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008562
PHENYL CHLOROFORMATE
1 spectrum
C7H5ClO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
155.99780
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008869
PHENYL ISOCYANATE
1 spectrum
C7H5NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
119.03711
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001370
Phenyl phosphate
5 spectra
C6H7O4P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
174.00819
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
MSBNK-Keio_Univ-KO003700
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
MSBNK-Keio_Univ-KO003701
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
MSBNK-Keio_Univ-KO003702
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
MSBNK-Keio_Univ-KO003703
LC-ESI-QQ; MS2; CE:50 V; [M+H]+
MSBNK-Keio_Univ-KO003704
PHENYL PROPIONATE
4 spectra
C9H10O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.06808
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005980
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP002542
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005915
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP006921
PHENYL PROPYL ETHER
1 spectrum
C9H12O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
136.08882
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004022
PHENYL SALICYLATE
1 spectrum
C13H10O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
214.06299
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008995
Phenyl styryl ketone, (E)-1,3-di(phenyl)prop-2-en-...
1 spectrum
C15H12O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
208.25999
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT100720
Phenyl styryl ketone, 1,3-Diphenyl-2-propenone, Ch...
6 spectra
C15H12O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
208.25999
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007201
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007202
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007203
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007204
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007205
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS007206
PHENYL SULFIDE
2 spectra
C12H10S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
186.05032
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005931
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005878
PHENYL TRIFLUOROACETATE
1 spectrum
C8H5F3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
190.02415
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP011271
PHENYL VINYL ETHER
1 spectrum
C8H8O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
120.05751
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP006788
phenyl(1,2,9,10-tetramethoxy-6-methyl-5,6-dihydro-...
5 spectra
C28H27NO5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
457.18893
LC-APCI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81927
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00820
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00830
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00840
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81925
PHENYL(1-PHENYLETHYL)BIS(TRIMETHYLSILYL)SILANE
1 spectrum
C20H32Si3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.18118
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP011682
PHENYL-3-TRIMETHYLSTANNYLPROPYL SULFIDE
1 spectrum
C12H20SSn
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
316.03076
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP004979
Phenyl-butyryl-glutamine
1 spectrum
C15H20N2O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
292.33499
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311145
PHENYL-MALONIC ACID BIS(TRIMETHYLSILYL) ESTER
1 spectrum
C15H24O4Si2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
324.12131
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP001035
PHENYL-N-PROPYL KETONE
1 spectrum
C10H12O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
148.08882
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005655
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