MassBank Record: ET080303



 LID_265.1546_9.2; 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: ET080303
RECORD_TITLE: LID_265.1546_9.2; 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 803

CH$NAME: LID_265.1546_9.2 CH$NAME: 2-[[2-(diethylamino)acetyl]amino]-3-methylbenzoic acid CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C14H20N2O3 CH$EXACT_MASS: 264.1474 CH$SMILES: O=C(Nc1c(C)cccc1C(=O)O)CN(CC)CC CH$IUPAC: InChI=1S/C14H20N2O3/c1-4-16(5-2)9-12(17)15-13-10(3)7-6-8-11(13)14(18)19/h6-8H,4-5,9H2,1-3H3,(H,15,17)(H,18,19) CH$LINK: PUBCHEM CID:19938477 CH$LINK: INCHIKEY ADEUTXKFSFCDGG-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 14247648
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 9.1 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 65.0598 MS$FOCUSED_ION: PRECURSOR_M/Z 265.1547 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$SPLASH: splash10-000i-9000000000-9d8006b9774812b315c2 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 55.018 C3H3O+ 1 55.0178 2.52 55.0545 C4H7+ 1 55.0542 4.06 57.0699 C4H9+ 1 57.0699 0.41 58.0652 C3H8N+ 1 58.0651 0.76 59.0491 C3H7O+ 1 59.0491 -0.02 67.0543 C5H7+ 1 67.0542 0.8 69.07 C5H9+ 1 69.0699 1.5 72.0444 C3H6NO+ 1 72.0444 0.83 73.0286 C3H5O2+ 1 73.0284 3.07 81.0699 C6H9+ 1 81.0699 0.16 86.0965 C5H12N+ 1 86.0964 0.98 87.0442 C4H7O2+ 1 87.0441 2 93.0701 C7H9+ 1 93.0699 2.18 95.0495 C6H7O+ 1 95.0491 3.56 95.0858 C7H11+ 1 95.0855 3.19 100.0758 C5H10NO+ 1 100.0757 1.3 101.0599 C5H9O2+ 1 101.0597 2.12 107.0855 C8H11+ 1 107.0855 -0.34 109.1014 C8H13+ 1 109.1012 1.68 115.0393 C5H7O3+ 1 115.039 3.12 119.0857 C9H11+ 1 119.0855 1.2 159.1168 C12H15+ 1 159.1168 -0.04 193.029 C13H5O2+ 1 193.0284 3.08 265.1538 C14H21N2O3+ 1 265.1547 -3.31 PK$NUM_PEAK: 24 PK$PEAK: m/z int. rel.int. 55.018 1011.8 1 55.0545 927.9 1 57.0699 5837.1 10 58.0652 15984.3 30 59.0491 5831 10 67.0543 850.3 1 69.07 2088.3 3 72.0444 15479.7 29 73.0286 1726 3 81.0699 1118.6 2 86.0965 532206 999 87.0442 4225.9 7 93.0701 1155.1 2 95.0495 1632.2 3 95.0858 1238.4 2 100.0758 17805 33 101.0599 1750.2 3 107.0855 1681.8 3 109.1014 1263.7 2 115.0393 4016.1 7 119.0857 1333.3 2 159.1168 1279.2 2 193.029 826.3 1 265.1538 848.8 1 //