MassBank Record: ET080506



 LID_180.1018_12.9; LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET080506
RECORD_TITLE: LID_180.1018_12.9; LC-ESI-QFT; MS2; CE: 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 Tentative identification: most likely structure (Level 3)
COMMENT: INTERNAL_ID 805

CH$NAME: LID_180.1018_12.9 CH$NAME: Acetamide, N-(2,6-dimethylphenyl)-2-hydroxy- CH$NAME: N-(2,6-dimethylphenyl)-2-hydroxyacetamide CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C10H13NO2 CH$EXACT_MASS: 179.0946 CH$SMILES: CC1=CC=CC(C)=C1NC(=O)CO CH$IUPAC: InChI=1S/C10H13NO2/c1-7-4-3-5-8(2)10(7)11-9(13)6-12/h3-5,12H,6H2,1-2H3,(H,11,13) CH$LINK: CAS 29183-14-0 CH$LINK: PUBCHEM CID:14480057 CH$LINK: INCHIKEY LUIJJBHAVXGCTP-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 11854678
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$MASS_SPECTROMETRY: COLLISION_ENERGY 90 (nominal) AC$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 12.7 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 65.0598 MS$FOCUSED_ION: PRECURSOR_M/Z 180.1019 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$SPLASH: splash10-0a4i-3900000000-e1c05f7e6c33cf630a8c PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 53.0386 C4H5+ 1 53.0386 1.01 65.0387 C5H5+ 1 65.0386 1.59 67.0544 C5H7+ 1 67.0542 3.18 79.0543 C6H7+ 1 79.0542 0.55 91.0544 C7H7+ 1 91.0542 1.46 93.0699 C7H9+ 1 93.0699 0.57 95.0493 C6H7O+ 1 95.0491 1.35 97.0077 C8H+ 1 97.0073 4.57 105.0701 C8H9+ 1 105.0699 2.32 106.0654 C7H8N+ 1 106.0651 3.06 107.0732 C7H9N+ 1 107.073 1.95 107.0851 C8H11+ 1 107.0855 -3.89 109.065 C7H9O+ 1 109.0648 2.1 111.0235 C9H3+ 1 111.0229 4.81 115.0541 C9H7+ 1 115.0542 -1.36 117.0576 C8H7N+ 1 117.0573 2.9 117.0702 C9H9+ 1 117.0699 2.93 118.065 C8H8N+ 1 118.0651 -0.9 119.0605 C7H7N2+ 1 119.0604 0.8 119.0732 C8H9N+ 1 119.073 2.09 119.0856 C9H11+ 1 119.0855 0.61 120.081 C8H10N+ 1 120.0808 1.45 122.0714 C6H8N3+ 1 122.0713 1.03 122.0965 C8H12N+ 1 122.0964 0.85 134.0964 C9H12N+ 1 134.0964 -0.27 135.0802 C9H11O+ 1 135.0804 -2.01 147.0683 C9H9NO+ 1 147.0679 3.16 PK$NUM_PEAK: 27 PK$PEAK: m/z int. rel.int. 53.0386 1394.7 39 65.0387 4629.5 130 67.0544 1539.4 43 79.0543 16779.1 471 91.0544 20264.8 569 93.0699 1394.2 39 95.0493 6103.2 171 97.0077 10949.8 307 105.0701 20192.5 567 106.0654 5718.6 160 107.0732 35566.4 999 107.0851 8781 246 109.065 1031 28 111.0235 4426.7 124 115.0541 3153 88 117.0576 1716.2 48 117.0702 1324.6 37 118.065 8054.1 226 119.0605 1694.3 47 119.0732 10551.3 296 119.0856 1313.7 36 120.081 10190 286 122.0714 1618 45 122.0965 9795.6 275 134.0964 10395 291 135.0802 6408.1 179 147.0683 3571.8 100 //