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( 2,701 - 2,809 Displayed )
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Name
Formula / Structure
ExactMass
ID
DI-STEARYL THIO-DI-PROPIONATE
1 spectrum
C42H82O4S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
682.59338
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003566
DI-TERT-BUTYL 2-PHENYL-1-PYRROLINE-TRANS-3,4-DICAR...
1 spectrum
C20H27NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
345.19400
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010268
Di-tert-butyl dicarbonate
6 spectra
C10H18O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
218.11542
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
MSBNK-Eawag-EQ315651
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
MSBNK-Eawag-EQ315652
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
MSBNK-Eawag-EQ315653
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
MSBNK-Eawag-EQ315654
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
MSBNK-Eawag-EQ315655
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
MSBNK-Eawag-EQ315656
DI-TERT-BUTYL MALONATE
1 spectrum
C11H20O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
216.13615
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009006
DI-TERT-BUTYL PEROXIDE
2 spectra
C8H18O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
146.13068
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP002888
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008319
DI-TERT-BUTYL SULFIDE
1 spectrum
C8H18S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
146.11292
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009129
Di-tert-butylphosphineoxide
16 spectra
C8H19OP
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
162.11740
LC-ESI-QTOF; MS2; 10 V
MSBNK-BAFG-CSL2311096093
LC-ESI-QTOF; MS2; 100 V
MSBNK-BAFG-CSL2311096103
LC-ESI-QTOF; MS2; 110 V
MSBNK-BAFG-CSL2311096098
LC-ESI-QTOF; MS2; 120 V
MSBNK-BAFG-CSL2311096099
LC-ESI-QTOF; MS2; 130 V
MSBNK-BAFG-CSL2311096089
LC-ESI-QTOF; MS2; 140 V
MSBNK-BAFG-CSL2311096095
LC-ESI-QTOF; MS2; 150 V
MSBNK-BAFG-CSL2311096102
LC-ESI-QTOF; MS2; 20 V
MSBNK-BAFG-CSL2311096088
LC-ESI-QTOF; MS2; 30 V
MSBNK-BAFG-CSL2311096091
LC-ESI-QTOF; MS2; 40 V
MSBNK-BAFG-CSL2311096092
LC-ESI-QTOF; MS2; 40 V
MSBNK-BAFG-CSL2311096096
LC-ESI-QTOF; MS2; 50 V
MSBNK-BAFG-CSL2311096097
LC-ESI-QTOF; MS2; 60 V
MSBNK-BAFG-CSL2311096100
LC-ESI-QTOF; MS2; 70 V
MSBNK-BAFG-CSL2311096101
LC-ESI-QTOF; MS2; 80 V
MSBNK-BAFG-CSL2311096094
LC-ESI-QTOF; MS2; 90 V
MSBNK-BAFG-CSL2311096090
Diacetolol
5 spectra
C16H24N2O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
308.17361
LC-ESI-Q; MS; POS; 15 V
MSBNK-Waters-WA001691
LC-ESI-Q; MS; POS; 30 V
MSBNK-Waters-WA001690
LC-ESI-Q; MS; POS; 45 V
MSBNK-Waters-WA001689
LC-ESI-Q; MS; POS; 60 V
MSBNK-Waters-WA001688
LC-ESI-Q; MS; POS; 75 V, 90 V
MSBNK-Waters-WA001687
Diacetone acrylamide
9 spectra
C9H15NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
169.11028
ESI-QTOF; MS2; CE: 10; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000074
ESI-QTOF; MS2; CE: 20; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000073
ESI-QTOF; MS2; CE: 40; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000075
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU049301
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU049302
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU049303
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU049304
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU049305
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU049306
Diacetoxyscirpenol
15 spectra
C19H26O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
366.16785
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000120
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+Na]+
MSBNK-AAFC-AC000125
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003518
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003519
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000121
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+Na]+
MSBNK-AAFC-AC000126
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000122
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+Na]+
MSBNK-AAFC-AC000127
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+H]+
MSBNK-AAFC-AC000123
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+Na]+
MSBNK-AAFC-AC000128
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004089
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004090
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+
MSBNK-AAFC-AC000124
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+Na]+
MSBNK-AAFC-AC000129
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004091
Diacetylmorphine (Heroin)
14 spectra
C21H23NO5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
369.15762
LC-ESI-Q; MS; POS; 15 V, 45 V
MSBNK-Waters-WA001030
LC-ESI-Q; MS; POS; 60 V
MSBNK-Waters-WA001029
LC-ESI-Q; MS; POS; 75 V
MSBNK-Waters-WA001028
LC-ESI-Q; MS; POS; 90 V
MSBNK-Waters-WA001027
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153301
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153302
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153303
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153304
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153305
LC-ESI-QTOF; MS2; HILIC; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153307
LC-ESI-QTOF; MS2; HILIC; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153308
LC-ESI-QTOF; MS2; HILIC; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153309
LC-ESI-QTOF; MS2; HILIC; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153310
LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU153311
Diadinochrome
2 spectra
C40H54O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
582.40729
FAB-EBEB; MS2; m/z: 582.41; [M]+*
MSBNK-Kyoto_Univ-CA000050
LC-ESI-QTOF; MS2; POSITIVE; ESI; [M+H]+; CE 20 V
MSBNK-MSSJ-MSJ00208
Dialifos
7 spectra
C14H17ClNO4PS2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
393.00250
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122807
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122801
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122802
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122803
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122804
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122805
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01122806
Diallate
8 spectra
C10H17Cl2NOS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
269.04080
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+ Isotopolog ion; CE 20 V
MSBNK-MSSJ-MSJ02275
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 10 V
MSBNK-MSSJ-MSJ02269
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 20 V
MSBNK-MSSJ-MSJ02270
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 30 V
MSBNK-MSSJ-MSJ02271
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 40 V
MSBNK-MSSJ-MSJ02272
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 50 V
MSBNK-MSSJ-MSJ02273
LC-ESI-QTOF; MS2; ESI; POSITIVE; [M+H]+; CE 60 V
MSBNK-MSSJ-MSJ02274
LC-ESI-QTOF; MS; ESI; POSITIVE
MSBNK-MSSJ-MSJ02268
DIALLYL ADIPATE
1 spectrum
C12H18O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
226.12051
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009018
DIALLYL DISULFIDE
1 spectrum
C6H10S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
146.02238
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009136
DIALLYL ETHER
1 spectrum
C6H10O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
98.07316
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP007209
DIALLYL FUMARATE
1 spectrum
C10H12O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
196.07356
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009000
DIALLYL MALEATE
2 spectra
C10H12O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
196.07356
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010602
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP010621
Diallyl phthalate
6 spectra
C14H14O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
246.08920
GC-APCI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU501801
GC-APCI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU501802
GC-APCI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU501803
GC-APCI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU501805
GC-APCI-QTOF; MS2; CE: 50 eV; R=35000; [M]+
MSBNK-Athens_Univ-AU501810
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
MSBNK-CASMI_2016-SM837002
DIALLYL PHTHALATE
3 spectra
C14H14O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
246.08920
CI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP006127
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP005813
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP008513
DIALLYL SULFIDE
1 spectrum
C6H10S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
114.05032
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP009125
Diallyldimethylammonium
3 spectra
[C8H16N]+
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
126.12827
ESI-QTOF; MS2; CE: 10; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001147
ESI-QTOF; MS2; CE: 20; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001148
ESI-QTOF; MS2; CE: 40; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001146
DIALLYLHYDRAZONE ACRYLALDEHYDE
1 spectrum
C9H14N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.11571
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP000869
DIALLYLHYDRAZONE PROPIONALDEHYDE
1 spectrum
C9H16N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
152.13135
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP000868
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