ACCESSION: MSBNK-RIKEN_ReSpect-PT204920
RECORD_TITLE: Pyridoxal hydrochrolide, Vitamin B6, Pyridoxaldehyde, PL-HCl, PL, 3-hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carbaldehyde, Hydroxy-5-hydroxymethyl-2-methylisonicotinaldehyde, 3-Hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinecarboxaldehyde; LC-ESI-QTOF; MS2
DATE: 2008.07.28
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$NAME: Pyridoxal hydrochrolide
CH$NAME: Vitamin B6
CH$NAME: Pyridoxaldehyde
CH$NAME: PL-HCl
CH$NAME: PL
CH$NAME: 3-hydroxy-5-(hydroxymethyl)-2-methylpyridine-4-carbaldehyde
CH$NAME: Hydroxy-5-hydroxymethyl-2-methylisonicotinaldehyde
CH$NAME: 3-Hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinecarboxaldehyde
CH$COMPOUND_CLASS: CLASS1 Other CLASS2 Vitamin
CH$FORMULA: C₈H₉NO₃
CH$EXACT_MASS: 167.164
CH$SMILES: CC1=NC=C(C(=C1O)C=O)CO
CH$IUPAC: InChI=1S/C8H9NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,4,10,12H,3H2,1H3
CH$LINK: CAS 66-72-8
CH$LINK: INCHIKEY RADKZDMFGJYCBB-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 166.05044

PK$SPLASH: splash10-05n0-0900000000-f468a00d88bedc116485
PK$NUM_PEAK: 4
PK$PEAK: m/z int. rel.int.
  108.0449 84.29 999
  136.0404 40.67 482
  138.0553 74.96 888
  166.0504 67.61 801
//