MassBank Record: UA004903



 3,3`-dichlorobenzidine; APCI-ITFT; MS2; CE: 35%; R=30000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: UA004903
RECORD_TITLE: 3,3`-dichlorobenzidine; APCI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
DATE: 2014.06.24
AUTHORS: C. Gallampois (Umea), E. Schymanski (Eawag), W. Brack (UFZ)
LICENSE: CC BY
COPYRIGHT: Copyright (C) Eawag, 2014
PUBLICATION: Multi-criteria approach for tentative identification of polyaromatic river mutagens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 49

CH$NAME: 3,3`-dichlorobenzidine CH$NAME: 4-(4-amino-3-chlorophenyl)-2-chloroaniline CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C12H10Cl2N2 CH$EXACT_MASS: 252.0221 CH$SMILES: Clc2cc(c1ccc(N)c(Cl)c1)ccc2N CH$IUPAC: InChI=1S/C12H10Cl2N2/c13-9-5-7(1-3-11(9)15)8-2-4-12(16)10(14)6-8/h1-6H,15-16H2 CH$LINK: CAS 91-94-1 CH$LINK: KEGG C19225 CH$LINK: PUBCHEM CID:7070 CH$LINK: INCHIKEY HUWXDEQWWKGHRV-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 6803
AC$INSTRUMENT: LTQ Orbitrap XL Thermo Scientific AC$INSTRUMENT_TYPE: APCI-ITFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: IONIZATION APCI AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID AC$MASS_SPECTROMETRY: COLLISION_ENERGY 35 % (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 30000 AC$CHROMATOGRAPHY: COLUMN_NAME N/A AC$CHROMATOGRAPHY: FLOW_GRADIENT Direct infusion experiment AC$CHROMATOGRAPHY: FLOW_RATE 5 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME N/A min AC$CHROMATOGRAPHY: SOLVENT A methanol AC$CHROMATOGRAPHY: SOLVENT B N/A
MS$FOCUSED_ION: BASE_PEAK 253.0294 MS$FOCUSED_ION: PRECURSOR_M/Z 253.0294 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1 MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included MS$DATA_PROCESSING: WHOLE RMassBank 1.5.2.3
PK$SPLASH: splash10-014i-0090000000-6bf20301de468424d354 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 181.0761 C12H9N2+ 1 181.076 0.36 182.0839 C12H10N2+ 1 182.0838 0.22 190.0419 C11H9ClN+ 1 190.0418 0.3 217.0525 C12H10ClN2+ 1 217.0527 -1.12 218.0602 C12H11ClN2+ 1 218.0605 -1.55 236.0025 C12H8Cl2N+ 1 236.0028 -1.57 252.0213 C12H10Cl2N2+ 1 252.0216 -1.09 253.0289 C12H11Cl2N2+ 1 253.0294 -1.78 PK$NUM_PEAK: 8 PK$PEAK: m/z int. rel.int. 181.0761 58689.3 16 182.0839 146161.5 40 190.0419 11903.5 3 217.0525 3595328.9 999 218.0602 1104145.2 306 236.0025 13074.5 3 252.0213 18818.2 5 253.0289 17182.1 4 //