ACCESSION: PR101042
RECORD_TITLE: Sinapic acid; LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
DATE: 2011.05.06 (Created 2009.09.10)
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-SA
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.
CH$NAME: Sinapic acid
CH$NAME: SA
CH$NAME: Sin
CH$NAME: Sinapate
CH$NAME: Sinapinic acid
CH$NAME: 3,5-dimethoxy-4-hydroxycinnamic acid
CH$NAME: 4-Hydroxy-3,5-dimethoxy-cinnamic acid
CH$COMPOUND_CLASS: Carboxylic acids
CH$FORMULA: C11H12O5
CH$EXACT_MASS: 224.06847
CH$SMILES: COc(c1)c(O)c(OC)cc(C=CC(O)=O)1
CH$IUPAC: InChI=1S/C11H12O5/c1-15-8-5-7(3-4-10(12)13)6-9(16-2)11(8)14/h3-6,14H,1-2H3,(H,12,13)/b4-3+
CH$LINK: CAS 530-59-6
CH$LINK: CHEMSPIDER 553361
CH$LINK: KAPPAVIEW KPC00975
CH$LINK: KEGG C00482
CH$LINK: KNAPSACK C00002776
CH$LINK: PUBCHEM CID:637775
AC$INSTRUMENT: UPLC Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-60 V
AC$MASS_SPECTROMETRY: DATAFORMAT Continuum
AC$MASS_SPECTROMETRY: DESOLVATION_GAS_FLOW 600.0 L/Hr
AC$MASS_SPECTROMETRY: DESOLVATION_TEMPERATURE 400 C
AC$MASS_SPECTROMETRY: FRAGMENTATION_METHOD LOW-ENERGY CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: SOURCE_TEMPERATURE 120 C
AC$CHROMATOGRAPHY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SAMPLING_CONE 23.0 V
AC$CHROMATOGRAPHY: SOLVENT CH3CN(0.1%HCOOH)/ H2O(0.1%HCOOH)
MS$FOCUSED_ION: PRECURSOR_M/Z 225.07629
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
PK$NUM_PEAK: 21
PK$PEAK: m/z int. rel.int.
  65.0428 157.1 131
  76.0351 79.62 67
  77.0423 72.16 60
  89.0421 160.9 134
  90.0501 74.6 62
  91.0579 766.6 640
  101.0428 62.32 52
  118.0453 152.7 128
  119.0529 678.3 567
  121.0325 88.13 74
  129.0368 105.9 88
  132.0246 82.1 69
  147.0487 528.1 441
  149.0279 234.8 196
  164.0514 91.32 76
  175.0440 841.7 703
  192.0477 339.5 284
  193.0053 108.9 91
  207.0704 1196 999
  209.0368 265.1 221
  225.0763 89.82 75
