ACCESSION: MSBNK-RIKEN_ReSpect-PT102810
RECORD_TITLE: Lys, (2S)-2,6-diaminohexanoic acid, (S)-2,6-Diaminohexanoic acid monohydrochloride, L-Lysine monohydrochloride, Lysine acid; LC-ESI-QTOF; MS2
DATE: 2008.07.25
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$NAME: Lys
CH$NAME: (2S)-2,6-diaminohexanoic acid
CH$NAME: (S)-2,6-Diaminohexanoic acid monohydrochloride
CH$NAME: L-Lysine monohydrochloride
CH$NAME: Lysine acid
CH$COMPOUND_CLASS: CLASS1 Amino acid CLASS2 Lysine
CH$FORMULA: C₆H₁₄N₂O₂
CH$EXACT_MASS: 146.19
CH$SMILES: C(CCN)CC(C(=O)O)N
CH$IUPAC: InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)
CH$LINK: CAS 56-87-1
CH$LINK: INCHIKEY KDXKERNSBIXSRK-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 POSITIVE
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 147.11332

PK$SPLASH: splash10-001i-9300000000-f81193f6b50235ec8147
PK$NUM_PEAK: 3
PK$PEAK: m/z int. rel.int.
  84.0807 652.0 999
  130.0865 210.4 322
  147.1133 57.56 88
//