ACCESSION: MSBNK-BGC_Munich-RP021411
RECORD_TITLE: 3-hydroxy-C6-homoserine lactone; LC-ESI-QTOF; MS2; CE: 10; R=; [M-H]-
DATE: 2017.11.29
AUTHORS: BGC, Helmholtz Zentrum Muenchen
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2017
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 214

CH$NAME: 3-hydroxy-C6-homoserine lactone
CH$NAME: 3OH-C6-HSL RS/RS
CH$NAME: 3-hydroxy-N-(2-oxooxolan-3-yl)hexanamide
CH$COMPOUND_CLASS: N/A; Metabolomics Standard
CH$FORMULA: C₁₀H₁₇NO₄
CH$EXACT_MASS: 215.1158
CH$SMILES: CCCC(O)CC(=O)NC1CCOC1=O
CH$IUPAC: InChI=1S/C10H17NO4/c1-2-3-7(12)6-9(13)11-8-4-5-15-10(8)14/h7-8,12H,2-6H2,1H3,(H,11,13)
CH$LINK: CAS 192883-16-2
CH$LINK: PUBCHEM CID:11579405
CH$LINK: INCHIKEY CRCIHGGZGGATGM-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 9754171

AC$INSTRUMENT: maXis plus UHR-ToF-MS, Bruker Daltonics
AC$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: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 10
AC$CHROMATOGRAPHY: COLUMN_NAME BEH C18 1.7um, 2.1x100mm, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 95/5 at 0 min, 95/5 at 1.12 min, 0.5/99.5 at 6.41 min, 0.5/99.5 at 10.01 min
AC$CHROMATOGRAPHY: FLOW_RATE 400 uL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 2.640 min
AC$CHROMATOGRAPHY: SOLVENT A Water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B ACN with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 214.1092
MS$FOCUSED_ION: PRECURSOR_M/Z 214.1085
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 2.4.0

PK$SPLASH: splash10-03dl-0980000000-ee7ba74301b1fe5d4266
PK$NUM_PEAK: 4
PK$PEAK: m/z int. rel.int.
  112.0406 326 144
  142.0515 1880 835
  143.0553 58 25
  214.1091 2248 999
//