MassBank Record: EQ340303



 5-Hydroxy Diclofenac; LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: EQ340303
RECORD_TITLE: 5-Hydroxy Diclofenac; LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
DATE: 2015.08.25
AUTHORS: Beck BDepartment of Environmental Chemistry, Eawag, Stravs MDepartment of Environmental Chemistry, Eawag, Schymanski EDepartment of Environmental Chemistry, Eawag, Singer HDepartment of Environmental Chemistry, Eawag, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2015 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 3403

CH$NAME: 5-Hydroxy Diclofenac CH$NAME: 5-hydroxydiclofenac CH$NAME: 2-[2-(2,6-dichloroanilino)-5-hydroxyphenyl]acetic acid CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C14H11Cl2NO3 CH$EXACT_MASS: 311.01160 CH$SMILES: C1=CC(=C(C(=C1)Cl)NC2=C(C=C(C=C2)O)CC(=O)O)Cl CH$IUPAC: InChI=1S/C14H11Cl2NO3/c15-10-2-1-3-11(16)14(10)17-12-5-4-9(18)6-8(12)7-13(19)20/h1-6,17-18H,7H2,(H,19,20) CH$LINK: CAS 69002-84-2 CH$LINK: CHEBI 59612 CH$LINK: PUBCHEM 3052566 CH$LINK: INCHIKEY VNQURRWYKFZKJZ-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 2314362
AC$INSTRUMENT: Q Exactive Plus Orbitrap Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-QFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD AC$MASS_SPECTROMETRY: COLLISION_ENERGY 45 (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 35000 AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5um, 2.1x50mm, Waters AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 50/50 at 4 min, 5/95 at 17 min, 5/95 at 25 min, 90/10 at 25.1 min, 90/10 at 30 min AC$CHROMATOGRAPHY: FLOW_RATE 200 ul/min AC$CHROMATOGRAPHY: RETENTION_TIME 10.3 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 312.0187 MS$FOCUSED_ION: PRECURSOR_M/Z 312.0189 MS$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$DATA_PROCESSING: WHOLE RMassBank 1.9.6
PK$SPLASH: splash10-001i-0090000000-7c40c222aa7bf45e4470 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 159.9716 C6H4Cl2N+ 2 159.9715 0.62 194.0603 C13H8NO+ 1 194.06 1.49 195.0679 C13H9NO+ 1 195.0679 0.33 196.0758 C13H10NO+ 1 196.0757 0.51 201.0341 C12H8ClN+ 1 201.034 0.36 202.0425 C12H9ClN+ 1 202.0418 3.2 214.0419 C13H9ClN+ 1 214.0418 0.54 224.0709 C14H10NO2+ 1 224.0706 1.45 229.0286 C13H8ClNO+ 1 229.0289 -1.45 230.0368 C13H9ClNO+ 1 230.0367 0.31 231.0445 C13H10ClNO+ 1 231.0445 -0.14 236.9924 C12HN2O4+ 1 236.9931 -3.01 237.9999 C12H2N2O4+ 1 238.0009 -4.28 259.0398 C14H10ClNO2+ 1 259.0395 1.32 266.0133 C13H10Cl2NO+ 1 266.0134 -0.36 277.0507 C14H12ClNO3+ 1 277.05 2.45 PK$NUM_PEAK: 16 PK$PEAK: m/z int. rel.int. 159.9716 162401.7 1 194.0603 592312.8 3 195.0679 1216986 7 196.0758 1454575.5 9 201.0341 269472.6 1 202.0425 227651.7 1 214.0419 1238142.9 7 224.0709 625882.9 3 229.0286 338345.8 2 230.0368 118289080 744 231.0445 158768656 999 236.9924 337576 2 237.9999 560418.2 3 259.0398 352086 2 266.0133 1399512.9 8 277.0507 349117.3 2 //