MassBank Record: ET030204



 CPP_329.1415_17.9; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET030204
RECORD_TITLE: CPP_329.1415_17.9; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
DATE: 2016.03.17 (Created 2015.09.25, modified 2016.02.03)
AUTHORS: R. Gulde, E. Schymanski, K. Fenner, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2016 Eawag, Duebendorf, Switzerland
PUBLICATION: Gulde, Meier, Schymanski, Kohler, Helbling, Derrer, Rentsch & Fenner; ES&T 2016 50(6):2908-2920. DOI: 10.1021/acs.est.5b05186. Systematic Exploration of Biotransformation Reactions of Amine-containing Micropollutants in Activated Sludge
COMMENT: CONFIDENCE Probable structure via diagnostic evidence, tentative identification (Level 2b)
COMMENT: INTERNAL_ID 302

CH$NAME: CPP_329.1415_17.9 CH$NAME: N-acetyl-1[(4-chlorophenyl)phenylmethyl]piperazine CH$NAME: 1-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethanone CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C19H21ClN2O CH$EXACT_MASS: 328.1342 CH$SMILES: CC(=O)N1CCN(CC1)C(C1=CC=CC=C1)C1=CC=C(Cl)C=C1 CH$IUPAC: InChI=1S/C19H21ClN2O/c1-15(23)21-11-13-22(14-12-21)19(16-5-3-2-4-6-16)17-7-9-18(20)10-8-17/h2-10,19H,11-14H2,1H3 CH$LINK: PUBCHEM CID:14070361 CH$LINK: INCHIKEY SQGNETKFPNXNSE-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 22773779
AC$INSTRUMENT: Q Exactive Plus Orbitrap Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-QFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD AC$MASS_SPECTROMETRY: COLLISION_ENERGY 60 (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 17500 AC$CHROMATOGRAPHY: COLUMN_NAME Atlantis T3 3um, 3x150mm, Waters with guard column AC$CHROMATOGRAPHY: FLOW_GRADIENT 95/5 at 0 min, 5/95 at 15 min, 5/95 at 20 min, 95/5 at 20.1 min, 95/5 at 25 min AC$CHROMATOGRAPHY: FLOW_RATE 300 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 17.3 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 65.0597 MS$FOCUSED_ION: PRECURSOR_M/Z 329.1415 MS$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$DATA_PROCESSING: WHOLE RMassBank 1.99.7
PK$SPLASH: splash10-00or-9510000000-d85d34a62b5051585587 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 53.0021 C3HO+ 1 53.0022 -1.91 53.9973 C2NO+ 1 53.9974 -2.04 74.0964 C4H12N+ 1 74.0964 0.06 77.0151 C3H6Cl+ 1 77.0153 -1.74 81.9814 CH3ClO2+ 1 81.9816 -2.91 165.0702 C13H9+ 1 165.0699 1.78 166.0773 C13H10+ 1 166.0777 -2.54 201.0457 C13H10Cl+ 2 201.0466 -4.45 PK$NUM_PEAK: 8 PK$PEAK: m/z int. rel.int. 53.0021 21058.3 117 53.9973 4941.7 27 74.0964 18649.8 104 77.0151 179111.4 999 81.9814 26931.9 150 165.0702 41543.3 231 166.0773 106175.8 592 201.0457 31405 175 //