ACCESSION: MSBNK-BAFG-CSL2311091164
RECORD_TITLE: 2-Phenylbenzimidazole; LC-ESI-QTOF; MS2; 110 V
DATE: 2023.11.09
AUTHORS: Kevin S. Jewell; Björn Ehlig; Arne Wick
LICENSE: dl-de/by-2-0
COPYRIGHT: Copyright 2023 Federal Institute of Hydrology, Koblenz, Germany
COMMENT: CONFIDENCE Reference Standard (Level 1)
COMMENT: Chromatography method: dx.doi.org/10.1016/j.chroma.2015.11.014
COMMENT: Acquisition method: 10.1002/rcm.8541

CH$NAME: 2-Phenylbenzimidazole
CH$COMPOUND_CLASS: Industrial_process
CH$FORMULA: C₁₃H₁₀N₂
CH$EXACT_MASS: 194.0844
CH$SMILES: [nH]1c2ccccc2nc1c3ccccc3
CH$IUPAC: InChI=1S/C13H10N2/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H,(H,14,15)
CH$LINK: CAS 716-79-0
CH$LINK: INCHIKEY DWYHDSLIWMUSOO-UHFFFAOYSA-N

AC$INSTRUMENT: TripleTOF 5600 SCIEX
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 110
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$CHROMATOGRAPHY: COLUMN_NAME Zorbax Eclipse Plus C18 2.1 mm x 150 mm, 3.5 um, Agilent
AC$CHROMATOGRAPHY: COLUMN_TEMPERATURE 40 °C
AC$CHROMATOGRAPHY: FLOW_GRADIENT 0 min min 98% A, 1 min 98% A, 2 min 80% A, 16.5 min 2% A, 22 min 2% A, 22.1 min 98% A, 27 min 98% A
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 5.903 min
AC$CHROMATOGRAPHY: SOLVENT A: Water 0.1% Formic acid, B: Acetonitrile 0.1% Formic acid

MS$FOCUSED_ION: PRECURSOR_M/Z 193.0771
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: COMMENT Export with Spectra 1.9.12 MsBackendMassbank 1.7.4
MS$DATA_PROCESSING: WHOLE RMassBank 2.3.1

PK$SPLASH: splash10-0w2c-9100000000-3d8a4c289aab47fb4f8a
PK$NUM_PEAK: 16
PK$PEAK: m/z int. rel.int.
  40.0105 0.1 124
  40.0352 0.1 124
  41.0153 0.2 249
  41.0234 0.2 249
  50.0052 0.8 999
  63.0121 0.3 374
  64.0091 0.1 124
  65.0162 0.1 124
  71.9995 0.1 124
  73.0085 0.1 124
  74.0046 0.2 249
  87.016 0.1 124
  88.0166 0.1 124
  90.0351 0.1 124
  115.0302 0.2 249
  141.0427 0.1 124
//