This website uses technical necessary cookies (e.g. session ID) and in addition the Matomo web analytics tool. Matomo enables us to evaluate the use of our website in compliance with GDPR (Directive 95/46/EC). Data Privacy Policy
This banner can be opend with the 'Data Privacy'-button. Your consent to the use of Matomo can be revoked any time. To make that choice, please un-check below.

MassBank MassBank Search Contents Download

MassBank Record: MSBNK-BGC_Munich-RP020402

C10-homoserine lactone; LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+

Mass Spectrum
50.00100.0150.0200.0250.0m/z0.000200.0400.0600.0800.01000Abundance
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-BGC_Munich-RP020402
RECORD_TITLE: C10-homoserine lactone; LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
DATE: 2017.10.25
AUTHORS: BGC, Helmholtz Zentrum Muenchen
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2017
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 204

CH$NAME: C10-homoserine lactone
CH$NAME: N-Decanoyl-DL-homoserine lactone
CH$NAME: N-(2-oxooxolan-3-yl)decanamide
CH$COMPOUND_CLASS: N/A; Metabolomics Standard
CH$FORMULA: C14H25NO3
CH$EXACT_MASS: 255.18344
CH$SMILES: CCCCCCCCCC(=O)NC1CCOC1=O
CH$IUPAC: InChI=1S/C14H25NO3/c1-2-3-4-5-6-7-8-9-13(16)15-12-10-11-18-14(12)17/h12H,2-11H2,1H3,(H,15,16)
CH$LINK: CAS 106983-36-2
CH$LINK: PUBCHEM CID:11644562
CH$LINK: INCHIKEY TZWZKDULKILUPV-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 9819301
CH$LINK: COMPTOX DTXSID30469949

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 POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 20
AC$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$CHROMATOGRAPHY: RETENTION_TIME 5.113 min
AC$CHROMATOGRAPHY: SOLVENT A Water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B ACN with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 256.1903
MS$FOCUSED_ION: PRECURSOR_M/Z 256.1907
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$SPLASH: splash10-0uej-9400000000-10b2fa37bb44e02a78ec
PK$NUM_PEAK: 25
PK$PEAK: m/z int. rel.int.
  59.048 358 2
  73.0642 1450 8
  74.023 11532 70
  79.0537 882 5
  81.0692 116514 713
  83.0849 6458 39
  84.044 7104 43
  85.1006 147716 904
  87.08 1138 6
  93.07 262 1
  95.0851 85276 522
  96.0884 5352 32
  97.101 1900 11
  99.0805 606 3
  100.0758 220 1
  102.0547 163100 999
  114.0547 378 2
  137.132 2732 16
  138.1359 344 2
  140.07 296 1
  155.1426 22184 135
  228.1953 610 3
  238.1798 15644 95
  239.1829 1892 11
  256.1909 1554 9
//

Imprint Feedback
system version 2.2.8

Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium

Responsible: Tillmann G. Fischer

Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under the National Research Data Infrastructure – NFDI4Chem – Projektnummer 441958208.

de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo