MassBank Record: ET150004



 PHE_241.1699_9.7; LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET150004
RECORD_TITLE: PHE_241.1699_9.7; LC-ESI-QFT; MS2; CE: 15-90; 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 Parent Substance with Reference Standard (Level 1)
COMMENT: INTERNAL_ID 1500

CH$NAME: PHE_241.1699_9.7 CH$NAME: Pheniramine CH$NAME: N,N-dimethyl-3-phenyl-3-pyridin-2-ylpropan-1-amine CH$COMPOUND_CLASS: N/A; Environmental Reference Standard CH$FORMULA: C16H20N2 CH$EXACT_MASS: 240.1626 CH$SMILES: CN(C)CCC(c1ccccc1)c1ccccn1 CH$IUPAC: InChI=1S/C16H20N2/c1-18(2)13-11-15(14-8-4-3-5-9-14)16-10-6-7-12-17-16/h3-10,12,15H,11,13H2,1-2H3 CH$LINK: CAS 86-21-5 CH$LINK: CHEBI 308661 CH$LINK: KEGG D08355 CH$LINK: PUBCHEM CID:4761 CH$LINK: INCHIKEY IJHNSHDBIRRJRN-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 4597
AC$INSTRUMENT: Q Exactive Orbitrap Thermo Scientific AC$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$MASS_SPECTROMETRY: COLLISION_ENERGY 15, 30, 45, 60, 70 or 90 (nominal) AC$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 9.9 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 241.1702 MS$FOCUSED_ION: PRECURSOR_M/Z 241.1699 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$SPLASH: splash10-0002-0900000000-a9b1b534a7a36bdaf014 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 91.0543 C7H7+ 1 91.0542 0.81 110.0601 C6H8NO+ 1 110.06 0.36 117.0574 C8H7N+ 1 117.0573 1.02 118.0651 C8H8N+ 1 118.0651 -0.39 119.0731 C8H9N+ 1 119.073 1.34 167.0732 C12H9N+ 1 167.073 1.37 168.0809 C12H10N+ 1 168.0808 0.74 180.0812 C13H10N+ 1 180.0808 2.47 181.0892 C13H11N+ 1 181.0886 3.09 194.0969 C14H12N+ 1 194.0964 2.49 195.105 C14H13N+ 1 195.1043 4.04 196.1122 C14H14N+ 1 196.1121 0.84 PK$NUM_PEAK: 12 PK$PEAK: m/z int. rel.int. 91.0543 2171268.2 29 110.0601 194134 2 117.0574 339147.9 4 118.0651 1886055.5 25 119.0731 335027.5 4 167.0732 9960222 136 168.0809 20107052 274 180.0812 259003.3 3 181.0892 248774.5 3 194.0969 697741.2 9 195.105 383902.6 5 196.1122 73139448 999 //