ACCESSION: MSBNK-Eawag-EA271112
RECORD_TITLE: Pirimicarb; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
DATE: 2014.01.14
AUTHORS: Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2012 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 2711

CH$NAME: Pirimicarb
CH$NAME: N,N-dimethylcarbamic acid [2-(dimethylamino)-5,6-dimethyl-4-pyrimidinyl] ester
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₁₁H₁₈N₄O₂
CH$EXACT_MASS: 238.1430
CH$SMILES: n(c(c(C)c1OC(=O)N(C)C)C)c(n1)N(C)C
CH$IUPAC: InChI=1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3
CH$LINK: CAS 23103-98-2
CH$LINK: CHEBI 8248
CH$LINK: KEGG C11079
CH$LINK: PUBCHEM CID:31645
CH$LINK: INCHIKEY YFGYUFNIOHWBOB-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 29348
CH$LINK: COMPTOX DTXSID1032569

AC$INSTRUMENT: LTQ Orbitrap XL Thermo Scientific
AC$INSTRUMENT_TYPE: LC-ESI-ITFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 75 % (nominal)
AC$MASS_SPECTROMETRY: RESOLUTION 15000
AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5um, 2.1x50mm, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 50/50 at 4 min, 5/95 at 17 min, 5/95 at 25 min, 90/10 at 25.1 min, 90/10 at 30 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 ul/min
AC$CHROMATOGRAPHY: RETENTION_TIME 5.0 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 239.1506
MS$FOCUSED_ION: PRECURSOR_M/Z 239.1503
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: DEPROFILE Spline
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 1.3.1

PK$SPLASH: splash10-00di-9200000000-23830c3be8a488b4d910
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  56.0131 C2H2NO+ 1 56.0131 0
  58.0652 C3H8N+ 1 58.0651 0.59
  71.0605 C3H7N2+ 1 71.0604 1.9
  72.0445 C3H6NO+ 1 72.0444 1.11
  83.0241 C3H3N2O+ 1 83.024 0.85
  85.0761 C4H9N2+ 1 85.076 0.65
  109.0761 C6H9N2+ 1 109.076 0.51
  124.0631 C6H8N2O+ 1 124.0631 -0.12
  137.071 C7H9N2O+ 1 137.0709 0.52
  138.0788 C7H10N2O+ 1 138.0788 0.19
  139.0867 C7H11N2O+ 1 139.0866 0.51
  150.1027 C8H12N3+ 1 150.1026 0.51
  152.0818 C7H10N3O+ 1 152.0818 -0.05
  156.0526 C6H8N2O3+ 1 156.0529 -1.88
  166.0974 C8H12N3O+ 1 166.0975 -0.65
  167.1053 C8H13N3O+ 1 167.1053 0.22
  180.1125 C9H14N3O+ 1 180.1131 -3.49
  182.129 C9H16N3O+ 1 182.1288 0.89
PK$NUM_PEAK: 18
PK$PEAK: m/z int. rel.int.
  56.0131 12782.8 1
  58.0652 17504.5 2
  71.0605 9777.7 1
  72.0445 6517575.2 999
  83.0241 156331.9 23
  85.0761 690779.4 105
  109.0761 582222.3 89
  124.0631 45902.1 7
  137.071 296137.1 45
  138.0788 285669.3 43
  139.0867 14709.4 2
  150.1027 185027.9 28
  152.0818 160944 24
  156.0526 23545.9 3
  166.0974 18694.3 2
  167.1053 134793.5 20
  180.1125 19851.2 3
  182.129 636765.2 97
//