MassBank Record: AU257402

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Epoxiconazole; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+

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

ACCESSION: AU257402
RECORD_TITLE: Epoxiconazole; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
DATE: 2019.05.29
AUTHORS: Nikiforos Alygizakis, Katerina Galani, Nikolaos Thomaidis, University of Athens
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2019 Department of Chemistry, University of Athens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 2574

CH$NAME: Epoxiconazole
CH$NAME: 1-[[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl]methyl]-1,2,4-triazole
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C17H13ClFN3O
CH$EXACT_MASS: 329.07311789999999973588273860514163970947265625
CH$SMILES: FC1=CC=C(C=C1)C1(CN2C=NC=N2)OC1C1=C(Cl)C=CC=C1
CH$IUPAC: InChI=1S/C17H13ClFN3O/c18-15-4-2-1-3-14(15)16-17(23-16,9-22-11-20-10-21-22)12-5-7-13(19)8-6-12/h1-8,10-11,16H,9H2
CH$LINK: CAS 135319-73-2
CH$LINK: CHEBI 83758
CH$LINK: CHEMSPIDER 2564795
CH$LINK: COMPTOX DTXSID1040372
CH$LINK: INCHIKEY ZMYFCFLJBGAQRS-UHFFFAOYSA-N
CH$LINK: PUBCHEM CID:3317081

AC$INSTRUMENT: Bruker maXis Impact
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 20 eV
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: RESOLUTION 35000
AC$CHROMATOGRAPHY: COLUMN_NAME Acclaim RSLC C18 2.2um, 2.1x100mm, Thermo
AC$CHROMATOGRAPHY: FLOW_GRADIENT 99/1 at 0-1 min, 61/39 at 3 min, 0.1/99.9 at 14-16 min, 99/1 at 16.1-20 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min at 0-3 min, 400 uL/min at 14 min, 480 uL/min at 16-19 min, 200 uL/min at 19.1-20 min
AC$CHROMATOGRAPHY: RETENTION_TIME 10.316 min
AC$CHROMATOGRAPHY: SOLVENT A 90:10 water:methanol with 0.01% formic acid and 5mM ammonium formate
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.01% formic acid and 5mM ammonium formate

MS$FOCUSED_ION: BASE_PEAK 330.0803
MS$FOCUSED_ION: PRECURSOR_M/Z 330.0804
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: RECALIBRATE identity on assigned fragments and MS1
MS$DATA_PROCESSING: WHOLE RMassBank 2.10.1

PK$SPLASH: splash10-00di-0902000000-f6ca1ef63d8d4dd8a6a0
PK$ANNOTATION: 121.0441 C8H6F+ 3 121.0448 -5.88
  122.0473 C7[13]CH6F+ 1 122.0487 -11.71
  123.0234 C5H2FN3+ 4 123.0227 5.3
  124.0266 C4[13]CH2FN3+ 1 124.0266 -0.49
  138.9935 C5H2ClN3+ 3 138.9932 2.66
  141.0089 C5H4ClN3+ 4 141.0088 0.66
  142.012 C4[13]CH4ClN3+ 1 142.0127 -5.07
  143.006 C5H4[37]ClN3+ 1 143.0064 -2.74
  149.0585 C7H7N3O+ 2 149.0584 1.24
  165.0532 C12H7N+ 1 165.0573 -24.74
  190.076 C10H9FN3+ 5 190.0775 -8
  261.047 C13H9ClFN3+ 3 261.0464 2.5
  330.0803 C17H14ClFN3O+ 1 330.0804 -0.2
  331.0833 C16[13]CH14ClFN3O+ 1 331.0843 -2.9
  332.0773 C17H14[37]ClFN3O+ 1 332.078 -1.96
PK$NUM_PEAK: 15
PK$PEAK: m/z int. rel.int.
  121.0441 582484 999
  122.0473 47988 82
  123.0234 158292 271
  124.0266 10864 18
  138.9935 11040 18
  141.0089 97480 167
  142.012 7316 12
  143.006 24596 42
  149.0585 3096 5
  165.0532 4988 8
  190.076 4100 7
  261.047 4428 7
  330.0803 175564 301
  331.0833 28868 49
  332.0773 48328 82
//