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MassBank Record: MSBNK-RIKEN_ReSpect-PT209760

L-alpha-Aminobutyric acid, (S)-2-Aminobutyric acid, (S)-2-Aminobutanoate, L-2-Aminobutyric acid, (2S)-2-aminobutanoic acid, L-2-Aminobutyrate, L-Butyrine, AABA, 2-ABU; LC-ESI-QTOF; MS2

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-RIKEN_ReSpect-PT209760
RECORD_TITLE: L-alpha-Aminobutyric acid, (S)-2-Aminobutyric acid, (S)-2-Aminobutanoate, L-2-Aminobutyric acid, (2S)-2-aminobutanoic acid, L-2-Aminobutyrate, L-Butyrine, AABA, 2-ABU; LC-ESI-QTOF; MS2
DATE: 2008.07.29
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-NC
COPYRIGHT: Copyright(C) 2009 Plant Science Center, RIKEN
COMMENT: Build 1 2009/06/24
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.

CH$NAME: L-alpha-Aminobutyric acid
CH$NAME: (S)-2-Aminobutyric acid
CH$NAME: (S)-2-Aminobutanoate
CH$NAME: L-2-Aminobutyric acid
CH$NAME: (2S)-2-aminobutanoic acid
CH$NAME: L-2-Aminobutyrate
CH$NAME: L-Butyrine
CH$NAME: AABA
CH$NAME: 2-ABU
CH$COMPOUND_CLASS: CLASS1 Other CLASS2 Carboxylic acid CLASS3 Butyric acid
CH$FORMULA: C4H9NO2
CH$EXACT_MASS: 103.121
CH$SMILES: CCC(C(=O)O)N
CH$IUPAC: InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
CH$LINK: CAS 1492-24-6
CH$LINK: INCHIKEY QWCKQJZIFLGMSD-UHFFFAOYSA-N

AC$INSTRUMENT: Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-45 V
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SOLVENT CH3CN/H2O

MS$FOCUSED_ION: ION_TYPE [M-H]-
MS$FOCUSED_ION: PRECURSOR_M/Z 102.05553

PK$SPLASH: splash10-0udi-0900000000-02624b93137883b214ad
PK$NUM_PEAK: 1
PK$PEAK: m/z int. rel.int.
  102.0555 46.53 999
//

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