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MassBank Record: MSBNK-LCSB-LU030006

Diphenylamine; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+

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

ACCESSION: MSBNK-LCSB-LU030006
RECORD_TITLE: Diphenylamine; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
DATE: 2020.08.19
AUTHORS: Kondić, T.;Singh, R.;Elapavalore, A.;Schymanski, E.
LICENSE: CC0
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 300
COMMENT: DATASET 20200303_ENTACT_RP_MIX505
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 9425
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 9420

CH$NAME: Diphenylamine
CH$NAME: N-phenylaniline
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C12H11N
CH$EXACT_MASS: 169.0891
CH$SMILES: N(C1=CC=CC=C1)C1=CC=CC=C1
CH$IUPAC: InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H
CH$LINK: CAS 122-39-4
CH$LINK: CHEBI 4640
CH$LINK: KEGG C11016
CH$LINK: PUBCHEM CID:11487
CH$LINK: INCHIKEY DMBHHRLKUKUOEG-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 11003

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$MASS_SPECTROMETRY: COLLISION_ENERGY 90
AC$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 18.046 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 170.0964
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 4125824.96875
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$SPLASH: splash10-0006-9000000000-7eff995a9905c8bb30ba
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  53.0386 C4H5+ 1 53.0386 0.68
  65.0385 C5H5+ 1 65.0386 -0.42
  66.0464 C5H6+ 1 66.0464 -0.25
  77.0385 C6H5+ 1 77.0386 -0.68
  92.0495 C6H6N+ 1 92.0495 0.54
  93.0573 C6H7N+ 1 93.0573 0.23
  94.0653 C6H8N+ 1 94.0651 2.2
  115.0543 C9H7+ 1 115.0542 0.5
  128.062 C10H8+ 1 128.0621 -0.3
  130.0652 C9H8N+ 1 130.0651 0.83
  141.07 C11H9+ 1 141.0699 0.63
  143.0729 C10H9N+ 1 143.073 -0.5
  143.0857 C11H11+ 1 143.0855 1.08
  152.0621 C12H8+ 1 152.0621 0.36
  153.07 C12H9+ 1 153.0699 0.58
  154.0652 C11H8N+ 1 154.0651 0.61
  154.0779 C12H10+ 1 154.0777 1.38
  155.073 C11H9N+ 1 155.073 0.13
  168.0812 C12H10N+ 1 168.0808 2.7
  169.089 C12H11N+ 1 169.0886 2.25
  170.0964 C12H12N+ 1 170.0964 0.1
PK$NUM_PEAK: 21
PK$PEAK: m/z int. rel.int.
  53.0386 10378.5 3
  65.0385 540455.6 168
  66.0464 156501.7 48
  77.0385 9105.6 2
  92.0495 566292.9 176
  93.0573 3196247.5 999
  94.0653 3533.1 1
  115.0543 8435 2
  128.062 34336.7 10
  130.0652 4372.2 1
  141.07 4120.2 1
  143.0729 4019.3 1
  143.0857 4309.6 1
  152.0621 149552.5 46
  153.07 34509.1 10
  154.0652 22804.2 7
  154.0779 3530.3 1
  155.073 8350.9 2
  168.0812 36852.3 11
  169.089 33570.5 10
  170.0964 42036.1 13
//

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