MassBank Record: ET170105



 PYR_302.1865_11.2; LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET170105
RECORD_TITLE: PYR_302.1865_11.2; LC-ESI-QFT; MS2; CE: 75; 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 1701

CH$NAME: PYR_302.1865_11.2 CH$NAME: Pyrilamine N-oxide CH$NAME: 2-[(4-methoxyphenyl)methyl-pyridin-2-ylamino]-N,N-dimethylethanamine oxide CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C17H23N3O2 CH$EXACT_MASS: 301.1790 CH$SMILES: COc1ccc(CN(CCN(C)(C)=O)c2ccccn2)cc1 CH$IUPAC: InChI=1S/C17H23N3O2/c1-20(2,21)13-12-19(17-6-4-5-11-18-17)14-15-7-9-16(22-3)10-8-15/h4-11H,12-14H2,1-3H3 CH$LINK: CAS 98982-99-1 CH$LINK: PUBCHEM CID:127200 CH$LINK: INCHIKEY IQDUZGGMNVZTAI-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 112904
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$MASS_SPECTROMETRY: COLLISION_ENERGY 75 (nominal) AC$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 11.1 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 61.0285 MS$FOCUSED_ION: PRECURSOR_M/Z 302.1863 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$SPLASH: splash10-00di-1900000000-3acfa63759901dc7f959 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 51.023 C4H3+ 1 51.0229 0.66 65.0386 C5H5+ 1 65.0386 -0.25 77.0384 C6H5+ 1 77.0386 -1.64 78.0464 C6H6+ 1 78.0464 -0.66 91.0542 C7H7+ 1 91.0542 -0.4 93.0699 C7H9+ 1 93.0699 -0.07 95.0491 C6H7O+ 1 95.0491 -0.64 96.0446 C5H6NO+ 1 96.0444 1.87 105.0447 C6H5N2+ 1 105.0447 -0.14 106.0413 C7H6O+ 1 106.0413 0.22 119.0603 C7H7N2+ 1 119.0604 -0.21 121.0648 C8H9O+ 1 121.0648 -0.34 PK$NUM_PEAK: 12 PK$PEAK: m/z int. rel.int. 51.023 3439 1 65.0386 11466.1 3 77.0384 28194.8 8 78.0464 66302.7 21 91.0542 187455.1 59 93.0699 19251.8 6 95.0491 98726.7 31 96.0446 6647 2 105.0447 71996.8 22 106.0413 32900.9 10 119.0603 24908.6 7 121.0648 3136501.5 999 //