MassBank Record: ET240303



 PRP_M258; LC-ESI-QFT; MS2; CE: 40; R=35000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: ET240303
RECORD_TITLE: PRP_M258; LC-ESI-QFT; MS2; CE: 40; R=35000; [M+H]+
DATE: 2016.03.01
AUTHORS: A. Roesch, E. Schymanski, J. Hollender, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2015 Eawag, Duebendorf, Switzerland
PUBLICATION: Roesch A, Anliker S, Hollender J, How Biotransformation Influences Toxicokinetics of Azole Fungicides in the Aquatic Invertebrate Gammarus pulex (submitted)
COMMENT: CONFIDENCE Transformation product, tentative ID (Level 2b)
COMMENT: INTERNAL_ID 2403

CH$NAME: PRP_M258 CH$NAME: 1-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethan-1-ol CH$NAME: 1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)ethanol CH$COMPOUND_CLASS: N/A; Environmental Transformation Products CH$FORMULA: C10H9Cl2N3O CH$EXACT_MASS: 257.0123 CH$SMILES: OC(CN1C=NC=N1)C1=C(Cl)C=C(Cl)C=C1 CH$IUPAC: InChI=1S/C10H9Cl2N3O/c11-7-1-2-8(9(12)3-7)10(16)4-15-6-13-5-14-15/h1-3,5-6,10,16H,4H2 CH$LINK: CAS 58905-18-3 CH$LINK: PUBCHEM 662857 CH$LINK: INCHIKEY XCWJBJOPHSVLGU-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 576592
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$MASS_SPECTROMETRY: COLLISION_ENERGY 40 (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 35000 AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5 um, 2.1x50 mm, Waters with guard column AC$CHROMATOGRAPHY: FLOW_GRADIENT 87/13/0 at 0 min, 7/93/0 at 20 min, 0/0/100 at 20.2-26 min, 87/13/0 at 26.2 min, 87/13/0 at 32.3 min AC$CHROMATOGRAPHY: FLOW_RATE 300 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 12.3 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT C isopropanol
MS$FOCUSED_ION: BASE_PEAK 212.1645 MS$FOCUSED_ION: PRECURSOR_M/Z 258.0195 MS$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$DATA_PROCESSING: WHOLE RMassBank 1.99.9
PK$SPLASH: splash10-00di-9000000000-e2d367e550cf397597fd PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 57.0699 C4H9+ 1 57.0699 0.02 59.0492 C3H7O+ 1 59.0491 1.1 62.0601 C2H8NO+ 1 62.06 0.67 67.0543 C5H7+ 1 67.0542 0.58 69.0699 C5H9+ 1 69.0699 -0.14 70.0399 C2H4N3+ 1 70.04 -0.47 71.0492 C4H7O+ 1 71.0491 0.86 79.0543 C6H7+ 1 79.0542 1.44 81.0699 C6H9+ 1 81.0699 0.01 83.0491 C5H7O+ 1 83.0491 -0.89 85.0648 C5H9O+ 1 85.0648 0.24 90.0173 H2N4O2+ 1 90.0172 1.22 91.0542 C7H7+ 1 91.0542 -0.05 93.0699 C7H9+ 1 93.0699 0.36 94.0733 C2H10N2O2+ 1 94.0737 -4.39 97.0649 C6H9O+ 1 97.0648 1.47 99.0442 C2H10ClNO+ 1 99.0445 -3.47 105.0698 C8H9+ 1 105.0699 -0.3 109.0648 C7H9O+ 1 109.0648 0.1 111.0441 C3H10ClNO+ 1 111.0445 -4.41 125.0152 C7H6Cl+ 1 125.0153 -0.39 146.9763 C6H5Cl2+ 1 146.9763 0.11 153.0101 C8H6ClO+ 2 153.0102 -0.32 170.9761 C8H5Cl2+ 1 170.9763 -1.2 188.9868 C8H7Cl2O+ 1 188.9868 -0.49 258.0194 C10H10Cl2N3O+ 1 258.0195 -0.48 PK$NUM_PEAK: 26 PK$PEAK: m/z int. rel.int. 57.0699 1889 2 59.0492 1042 1 62.0601 929.4 1 67.0543 7092 8 69.0699 8868.7 10 70.0399 880559.6 999 71.0492 1542.8 1 79.0543 1145.1 1 81.0699 14103.9 16 83.0491 1526.2 1 85.0648 1767.8 2 90.0173 29220.6 33 91.0542 1903 2 93.0699 7345.5 8 94.0733 1045 1 97.0649 2015.5 2 99.0442 1196.2 1 105.0698 4036.4 4 109.0648 1082.1 1 111.0441 5318.7 6 125.0152 32615.5 37 146.9763 5170.4 5 153.0101 24478.7 27 170.9761 11045.6 12 188.9868 17558.5 19 258.0194 19518.3 22 //