MassBank Record: LIT00020

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1COOH-2But-A7EO3; LC-ESI-Q; MS2; 30 V; [M+H]+

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: LIT00020
RECORD_TITLE: 1COOH-2But-A7EO3; LC-ESI-Q; MS2; 30 V; [M+H]+
DATE: 2016.02.03 (Created 2013.04.15)
AUTHORS: E. Schymanski; retrieved from A. Di Corcia et al. 1998
LICENSE: CC0
COPYRIGHT: Copyright (C) American Chemical Society 1998
PUBLICATION: Corcia, A. D.; Crescenzi, C.; Marcomini, A.; Samperi, R. Liquid Chromatography- Electrospray-Mass Spectrometry as a Valuable Tool for Characterizing Biodegradation Intermediates of Branched Alcohol Ethoxylate Surfactants. Environmental Science & Technology 1998, 32 (5), 711–8. DOI:10.1021/es970616x
COMMENT: Literature spectrum
COMMENT: CONFIDENCE Tentative identification: isomers possible (Level 3)
COMMENT: Could be alkyl homologue of given structure
COMMENT: Digitised from figure: approximate intensities

CH$NAME: 1COOH-2But-A7EO3
CH$NAME: 1-Carboxyl-2-butyl-A7EO3
CH$NAME: 3-({2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}methyl)heptanoic acid
CH$COMPOUND_CLASS: N/A; Surfactant
CH$FORMULA: C14H28O6
CH$EXACT_MASS: 292.1886
CH$SMILES: OCCOCCOCCOCC(CC(=O)O)CCCC
CH$IUPAC: InChI=1S/C14H28O6/c1-2-3-4-13(11-14(16)17)12-20-10-9-19-8-7-18-6-5-15/h13,15H,2-12H2,1H3,(H,16,17)
CH$LINK: INCHIKEY JHOXVFIHEZNGJK-UHFFFAOYSA-N
CH$LINK: COMPTOX DTXSID90891646
CH$LINK: PUBCHEM CID:137628421

AC$INSTRUMENT: Fisons VG Platform
AC$INSTRUMENT_TYPE: LC-ESI-Q
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 30 V

MS$FOCUSED_ION: BASE_PEAK 293.1959
MS$FOCUSED_ION: PRECURSOR_M/Z 293.1959
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: WHOLE Hand-digitised from figures

PK$SPLASH: splash10-003i-9841000000-16cd9580e3af3d29cebc
PK$ANNOTATION: m/z formula putative_smiles
  45 C2H5O+ [CH2+]CO
  45 CHO2+ O=[C+]O
  89 C4H9O2+ [CH2+]COCCO
  133 C6H13O3+ OCCOCCOC[CH2+]
  275 C14H27O5+ O=C(O)CC(CCCC)COCCOCCOC[CH2+]
  293 C14H29O6+ OCCOCCOCCOCC(CC(=[OH+])O)CCCC
  315 C14H28O6Na+ [M+Na]+
  331 C14H28O6K+ [M+K]+
PK$NUM_PEAK: 10
PK$PEAK: m/z int. rel.int.
  45 35 350
  89 100 999
  125 5 50
  133 95 950
  143 10 100
  169 10 100
  275 50 500
  293 15 150
  315 15 150
  331 5 50
//