MassBank Record: ET110503



 NPE_269.1647_12.5; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET110503
RECORD_TITLE: NPE_269.1647_12.5; LC-ESI-QFT; MS2; CE: 45; 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 Tentative identification: most likely structure (Level 3)
COMMENT: INTERNAL_ID 1105

CH$NAME: NPE_269.1647_12.5 CH$NAME: Norpheniramine acetate CH$NAME: N-methyl-N-(3-phenyl-3-pyridin-2-ylpropyl)acetamide CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C17H20N2O CH$EXACT_MASS: 268.1576 CH$SMILES: CN(CCC(C1=CC=CC=C1)C1=NC=CC=C1)C(C)=O CH$IUPAC: InChI=1S/C17H20N2O/c1-14(20)19(2)13-11-16(15-8-4-3-5-9-15)17-10-6-7-12-18-17/h3-10,12,16H,11,13H2,1-2H3 CH$LINK: PUBCHEM CID:524050 CH$LINK: INCHIKEY VLRZUFDFIGKGCN-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 457020
AC$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 45 (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$CHROMATOGRAPHY: RETENTION_TIME 12.2 min AC$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$FOCUSED_ION: PRECURSOR_M/Z 269.1648 MS$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: splash10-0002-0900000000-11719ab4fc6d6abcc855 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 55.0541 C4H7+ 1 55.0542 -2.85 57.0697 C4H9+ 1 57.0699 -2.4 69.0697 C5H9+ 1 69.0699 -2.27 71.0853 C5H11+ 1 71.0855 -3.19 81.0698 C6H9+ 1 81.0699 -0.7 93.07 C7H9+ 1 93.0699 0.79 95.0854 C7H11+ 1 95.0855 -1.02 107.0853 C8H11+ 1 107.0855 -1.74 109.1009 C8H13+ 1 109.1012 -2.81 125.0599 C7H9O2+ 1 125.0597 1.63 135.0801 C9H11O+ 1 135.0804 -2.68 167.0725 C12H9N+ 1 167.073 -2.46 168.0811 C12H10N+ 1 168.0808 2.11 196.112 C14H14N+ 1 196.1121 -0.28 269.1644 C17H21N2O+ 1 269.1648 -1.56 PK$NUM_PEAK: 15 PK$PEAK: m/z int. rel.int. 55.0541 1593.6 4 57.0697 4623.1 13 69.0697 4158.1 12 71.0853 984.2 2 81.0698 4215.2 12 93.07 1323 3 95.0854 4107.8 12 107.0853 1329.8 3 109.1009 1055.8 3 125.0599 991.9 2 135.0801 865.4 2 167.0725 4032 11 168.0811 7077.2 20 196.112 337277.3 999 269.1644 1608.6 4 //