Record Index Results
Search
Contents
Download
Documentation
About MassBank
News Archive
Index Type :
Instrument Type:
LC-ESI-ITFT
Back to Record Index
Results :
20,038 Hit.
( 942 - 1,093 Displayed )
First
Prev
1
2
3
4
5
6
7
8
9
10
Next
Last
( Total
71
Page )
▼
Results End
Name
Formula / Structure
ExactMass
ID
3'-AMP
2 spectra
C10H14N5O7P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
347.06311
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-MetaboLights-ML001101
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-MetaboLights-ML001151
3,15-Diacetyldeoxynivalenol
5 spectra
C19H24O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
380.14709
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000115
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000116
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000117
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+H]+
MSBNK-AAFC-AC000118
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+
MSBNK-AAFC-AC000119
3,3-pentamethylene-4-butyrolactam
3 spectra
C9H15NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
153.11540
LC-ESI-ITFT; MS2; CE: 35 eV; R=30000; [M+H]+
MSBNK-KWR-KW100303
LC-ESI-ITFT; MS2; CE: 35 eV; R=7500; [M+H]+
MSBNK-KWR-KW100302
LC-ESI-ITFT; MS2; CE: 65 eV; R=30000; [M+H]+
MSBNK-KWR-KW100304
3,4,5-Trimethoxycinnamic_acid
5 spectra
C12H14O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
238.08414
LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000098
LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000099
LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000100
LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
MSBNK-MPI_for_Chemical_Ecology-CE000101
LC-ESI-ITFT; MS; [M+H]+; isotope pattern
MSBNK-MPI_for_Chemical_Ecology-CE000102
3,4-Dichlorophenylurea
8 spectra
C7H6Cl2N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
203.98570
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF405203
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M-H]-
MSBNK-UFZ-UF405253
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF405201
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF405204
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M-H]-
MSBNK-UFZ-UF405251
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M-H]-
MSBNK-UFZ-UF405254
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF405202
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M-H]-
MSBNK-UFZ-UF405252
3,5,6-Trichloro-2-pyridinol
10 spectra
C5H2Cl3NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
196.92020
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA270458
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA270452
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA270459
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA270453
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M-H]-
MSBNK-Eawag-EA270464
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA270451
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA270460
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA270454
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
MSBNK-Eawag-EA270461
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-Eawag-EA270455
3,5-Dibromo-4-hydroxybenzoic acid
14 spectra
C7H4Br2O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
293.85269
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA080458
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA080452
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA080459
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA080453
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M-H]-
MSBNK-Eawag-EA080464
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA080451
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA080460
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA080454
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
MSBNK-Eawag-EA080461
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-Eawag-EA080455
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M-H]-
MSBNK-Eawag-EA080462
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M-H]-
MSBNK-Eawag-EA080456
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M-H]-
MSBNK-Eawag-EA080463
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA080457
3,9-dicyclohex-3-enyl-2,4,8,10-tetraoxaspiro[5.5]u...
4 spectra
C19H28O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
320.19879
LC-ESI-ITFT; MS2; CE: 35 eV; R=30000; [M+H]+
MSBNK-KWR-KW107003
LC-ESI-ITFT; MS2; CE: 35 eV; R=7500; [M+H]+
MSBNK-KWR-KW107002
LC-ESI-ITFT; MS2; CE: 35 eV; R=nominal; [M+H]+
MSBNK-KWR-KW107001
LC-ESI-ITFT; MS2; CE: 65 eV; R=30000; [M+H]+
MSBNK-KWR-KW107004
3-Acetyldeoxynivalenol
6 spectra
C17H22O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
338.13660
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002970
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002972
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002974
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002971
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002973
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002975
3-Aminoacetophenon
6 spectra
C8H9NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
135.06842
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-UFZ-WANA264801AD6CPH
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-UFZ-WANA264803B085PH
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-UFZ-WANA264805070APH
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-UFZ-WANA264811C9CFPH
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-UFZ-WANA264813D9F1PH
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-UFZ-WANA2648155BE0PH
3-aminobenzoic acid
1 spectrum
C7H7NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
137.04770
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-MetaboLights-ML001001
3-coumaric acid
1 spectrum
C9H8O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
164.04730
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-MetaboLights-ML001251
3-hydroxybenzoic acid
1 spectrum
C7H6O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
138.03169
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-MetaboLights-ML001351
3-Hydroxypropyl-Glucosinolate
18 spectra
C10H19NO10S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
377.04504
LC-ESI-ITFT; MS2; HCD; CE 10.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000522
LC-ESI-ITFT; MS2; HCD; CE 15.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000513
LC-ESI-ITFT; MS2; HCD; CE 20.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000517
LC-ESI-ITFT; MS2; HCD; CE 25.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000514
LC-ESI-ITFT; MS2; HCD; CE 30.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000518
LC-ESI-ITFT; MS2; HCD; CE 35.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000516
LC-ESI-ITFT; MS2; HCD; CE 40.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000520
LC-ESI-ITFT; MS2; HCD; CE 45.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000519
LC-ESI-ITFT; MS2; HCD; CE 5.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000515
LC-ESI-ITFT; MS2; HCD; CE 50.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000521
LC-ESI-ITFT; MS2; HCD; CE 55.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000510
LC-ESI-ITFT; MS2; HCD; CE 60.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000507
LC-ESI-ITFT; MS2; HCD; CE 65.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000505
LC-ESI-ITFT; MS2; HCD; CE 70.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000512
LC-ESI-ITFT; MS2; HCD; CE 75.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000509
LC-ESI-ITFT; MS2; HCD; CE 80.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000508
LC-ESI-ITFT; MS2; HCD; CE 85.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000511
LC-ESI-ITFT; MS2; HCD; CE 90.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000506
3-Iodopropynyl butylcarbamate
4 spectra
C8H12INO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
280.99130
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF418403
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF418401
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF418404
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF418402
3-methyl-2-oxovaleric acid
1 spectrum
C6H10O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
130.06300
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-MetaboLights-ML001451
3-Methylthiopropyl-Glucosinolate
18 spectra
C11H21NO9S3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
407.03784
LC-ESI-ITFT; MS2; HCD; CE 10.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000561
LC-ESI-ITFT; MS2; HCD; CE 15.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000552
LC-ESI-ITFT; MS2; HCD; CE 20.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000556
LC-ESI-ITFT; MS2; HCD; CE 25.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000553
LC-ESI-ITFT; MS2; HCD; CE 30.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000557
LC-ESI-ITFT; MS2; HCD; CE 35.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000555
LC-ESI-ITFT; MS2; HCD; CE 40.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000559
LC-ESI-ITFT; MS2; HCD; CE 45.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000558
LC-ESI-ITFT; MS2; HCD; CE 5.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000554
LC-ESI-ITFT; MS2; HCD; CE 50.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000560
LC-ESI-ITFT; MS2; HCD; CE 55.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000549
LC-ESI-ITFT; MS2; HCD; CE 60.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000546
LC-ESI-ITFT; MS2; HCD; CE 65.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000544
LC-ESI-ITFT; MS2; HCD; CE 70.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000551
LC-ESI-ITFT; MS2; HCD; CE 75.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000548
LC-ESI-ITFT; MS2; HCD; CE 80.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000547
LC-ESI-ITFT; MS2; HCD; CE 85.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000550
LC-ESI-ITFT; MS2; HCD; CE 90.0 eV; [M-H]-
MSBNK-MPI_for_Chemical_Ecology-CE000545
3-Phenoxybenzoic acid
17 spectra
C13H10O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
214.06300
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
MSBNK-Eawag-EA032658
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-Eawag-EA032652
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA032609
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
MSBNK-Eawag-EA032659
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-Eawag-EA032653
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA032614
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M-H]-
MSBNK-Eawag-EA032664
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA032601
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
MSBNK-Eawag-EA032651
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
MSBNK-Eawag-EA032660
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
MSBNK-Eawag-EA032654
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
MSBNK-Eawag-EA032661
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-Eawag-EA032655
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M-H]-
MSBNK-Eawag-EA032662
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M-H]-
MSBNK-Eawag-EA032656
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M-H]-
MSBNK-Eawag-EA032663
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
MSBNK-Eawag-EA032657
3-Phenoxybenzylalcohol
10 spectra
C13H12O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
200.08369
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-Eawag-EA032508
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-Eawag-EA032502
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-Eawag-EA032509
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-Eawag-EA032503
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-Eawag-EA032514
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-Eawag-EA032501
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-Eawag-EA032510
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-Eawag-EA032504
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-Eawag-EA032511
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-Eawag-EA032506
3-Phospho-D-glycerate
1 spectrum
C3H7O7P
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
185.99294
LC-ESI-ITFT; MS2; m/z:184.99; NEG
MSBNK-NAIST-KNA00822
4',5-bisdeoxy-dothistromin
5 spectra
C18H12O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
340.05829
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
MSBNK-AAFC-AC000921
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
MSBNK-AAFC-AC000922
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-AAFC-AC000923
LC-ESI-ITFT; MS2; CE: 35; R=17500; [M+H]+
MSBNK-AAFC-AC000924
LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+
MSBNK-AAFC-AC000925
4,(6or7)-dimethyl benzotriazole (Tentative)
1 spectrum
C8H9N3
147.07961
LC-ESI-ITFT; MS2; 80-110; R=7500; [M+H]+
MSBNK-Eawag_Additional_Specs-ETS00100
4,4?-Dichlorobenzophenone
4 spectra
C13H8Cl2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
249.99519
LC-ESI-ITFT; MS2; CE: 35 eV; R=30000; [M+H]+
MSBNK-KWR-KW106803
LC-ESI-ITFT; MS2; CE: 35 eV; R=7500; [M+H]+
MSBNK-KWR-KW106802
LC-ESI-ITFT; MS2; CE: 35 eV; R=nominal; [M+H]+
MSBNK-KWR-KW106801
LC-ESI-ITFT; MS2; CE: 65 eV; R=30000; [M+H]+
MSBNK-KWR-KW106804
4,4`-Methylen-bis(2-methyl aniline)
4 spectra
C15H18N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
226.14700
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
MSBNK-UFZ-UF414203
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF414201
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
MSBNK-UFZ-UF414204
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
MSBNK-UFZ-UF414202
4,4`-Methylene-bis(2-methyl aniline)
3 spectra
C15H18N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
226.14700
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-UFZ-WANA0379213166PH
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-UFZ-WANA0379237762PH
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-UFZ-WANA037925AF82PH
First
Prev
1
2
3
4
5
6
7
8
9
10
Next
Last
( Total
71
Page )
▲
Results Top
Imprint
Feedback
system version 2.2.5
Copyright © 2006 MassBank Project; 2011
NORMAN Association
; 2021
MassBank Consortium
Responsible:
Hannes Bohring