ACCESSION: MSBNK-LCSB-LU058602
RECORD_TITLE: Dimethenamid; LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
DATE: 2020.08.19
AUTHORS: Elapavalore, A.; Kondić, T.; Singh, R.; Schymanski, E.
LICENSE: CC BY
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
PUBLICATION: Elapavalore, A.; Kondić, T.; et al., Adding Open Spectral Data to MassBank and PubChem Using Open Source Tools to Support Non-Targeted Exposomics of Mixtures (submitted).
PROJECT: ENTACT U.S. Environmental Protection Agency’s Non-Targeted Analysis Collaborative Trial
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 586
COMMENT: DATASET 20200303_ENTACT_RP_MIX506
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 9100
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 9097
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]

CH$NAME: Dimethenamid
CH$NAME: 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₁₂H₁₈ClNO₂S
CH$EXACT_MASS: 275.0747
CH$SMILES: COCC(C)N(C(=O)CCl)C1=C(C)SC=C1C
CH$IUPAC: InChI=1S/C12H18ClNO2S/c1-8-7-17-10(3)12(8)14(11(15)5-13)9(2)6-16-4/h7,9H,5-6H2,1-4H3
CH$LINK: CAS 87674-68-8
CH$LINK: CHEBI 83638
CH$LINK: KEGG C18499
CH$LINK: PUBCHEM CID:91744
CH$LINK: INCHIKEY JLYFCTQDENRSOL-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 82842

AC$INSTRUMENT: Q Exactive Orbitrap (Thermo Scientific)
AC$INSTRUMENT_TYPE: LC-ESI-QFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 30
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity BEH C18 1.7um, 2.1x150mm (Waters)
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0-2 min, 0/100 at 15-20 min, 90/10 at 20.1-30 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.20 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 17.366 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol

MS$FOCUSED_ION: BASE_PEAK 79.0211
MS$FOCUSED_ION: PRECURSOR_M/Z 276.082
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 13996987.625
MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 2.99.2

PK$SPLASH: splash10-0006-0390000000-ffe53b9f98aee9b08538
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  73.0647 C4H9O+ 2 73.0648 -0.59
  76.9789 C2H2ClO+ 1 76.9789 0.16
  91.0541 C7H7+ 1 91.0542 -1.07
  93.0698 C7H9+ 1 93.0699 -1.17
  111.0263 C6H7S+ 1 111.0263 -0.22
  116.0262 C5H7ClN+ 2 116.0262 0.04
  121.0648 C8H9O+ 2 121.0648 -0.12
  138.9945 C7H4ClO+ 1 138.9945 0.05
  151.0575 C9H11S+ 2 151.0576 -0.85
  152.0167 C7H6NOS+ 1 152.0165 1.66
  166.0684 C9H12NS+ 2 166.0685 -0.3
  167.0763 C9H13NS+ 2 167.0763 0.09
  168.0842 C9H14NS+ 2 168.0841 0.2
  186.0139 C8H9ClNS+ 2 186.0139 -0.09
  204.0245 C8H11ClNOS+ 2 204.0244 0.13
  244.0557 C11H15ClNOS+ 1 244.0557 -0.02
  276.0804 C12H19ClNO2S+ 1 276.082 -5.74
PK$NUM_PEAK: 17
PK$PEAK: m/z int. rel.int.
  73.0647 87755.5 15
  76.9789 5908.8 1
  91.0541 6037.4 1
  93.0698 8112.4 1
  111.0263 29079.6 5
  116.0262 10524.9 1
  121.0648 456799.3 82
  138.9945 725975.9 130
  151.0575 24429.5 4
  152.0167 5996.8 1
  166.0684 7150.3 1
  167.0763 24239.8 4
  168.0842 570845.5 102
  186.0139 22650 4
  204.0245 24455.3 4
  244.0557 5538443 999
  276.0804 57755.5 10
//