MassBank Record: EA014612



 Fenpropimorph; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: EA014612
RECORD_TITLE: Fenpropimorph; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
DATE: 2014.01.14
AUTHORS: Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2012 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 146

CH$NAME: Fenpropimorph CH$NAME: (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methyl-propyl]-2,6-dimethyl-morpholine CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C20H33NO CH$EXACT_MASS: 303.2557 CH$SMILES: CC1CN(CC(O1)C)CC(C)CC2=CC=C(C=C2)C(C)(C)C CH$IUPAC: InChI=1S/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3/t15?,16-,17+ CH$LINK: CAS 67306-03-0 CH$LINK: CHEBI 50145 CH$LINK: PUBCHEM CID:93365 CH$LINK: INCHIKEY RYAUSSKQMZRMAI-ALOPSCKCSA-N CH$LINK: CHEMSPIDER 84290
AC$INSTRUMENT: LTQ Orbitrap XL Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-ITFT 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 15000 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 9.4 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 304.2639 MS$FOCUSED_ION: PRECURSOR_M/Z 304.2635 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: DEPROFILE Spline MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1 MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included MS$DATA_PROCESSING: WHOLE RMassBank 1.3.1
PK$SPLASH: splash10-0002-1900000000-937ff2c484d12b6bfbca PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 56.0494 C3H6N+ 1 56.0495 -1.17 57.0698 C4H9+ 1 57.0699 -1.34 58.0651 C3H8N+ 1 58.0651 -1.13 59.0491 C3H7O+ 1 59.0491 -1.21 70.0651 C4H8N+ 1 70.0651 0.06 72.0807 C4H10N+ 1 72.0808 -1.47 79.054 C6H7+ 1 79.0542 -2.49 81.0699 C6H9+ 1 81.0699 0.29 86.0966 C5H12N+ 1 86.0964 2.6 88.0757 C4H10NO+ 1 88.0757 0.34 91.0542 C7H7+ 1 91.0542 -0.07 93.0698 C7H9+ 1 93.0699 -1.15 98.0964 C6H12N+ 1 98.0964 -0.06 102.0914 C5H12NO+ 1 102.0913 0.68 104.0622 C8H8+ 1 104.0621 1.04 105.0699 C8H9+ 1 105.0699 -0.16 107.0855 C8H11+ 1 107.0855 -0.16 112.1122 C7H14N+ 1 112.1121 1.29 116.107 C6H14NO+ 1 116.107 -0.09 117.0698 C9H9+ 1 117.0699 -0.4 119.0855 C9H11+ 1 119.0855 -0.06 130.1226 C7H16NO+ 1 130.1226 -0.62 131.0852 C10H11+ 1 131.0855 -2.72 132.0933 C10H12+ 1 132.0934 -0.32 145.1011 C11H13+ 1 145.1012 -0.25 146.1088 C11H14+ 1 146.109 -1.18 147.1168 C11H15+ 1 147.1168 -0.05 159.1167 C12H15+ 1 159.1168 -0.99 161.1324 C12H17+ 1 161.1325 -0.35 PK$NUM_PEAK: 29 PK$PEAK: m/z int. rel.int. 56.0494 45941.5 9 57.0698 295429.7 60 58.0651 26586.6 5 59.0491 44951.5 9 70.0651 77867.7 15 72.0807 26238.4 5 79.054 29716.3 6 81.0699 70820.1 14 86.0966 22614.9 4 88.0757 33624.5 6 91.0542 256769.6 52 93.0698 27298.6 5 98.0964 1441601.4 293 102.0914 55669.2 11 104.0622 20172.8 4 105.0699 1107103.7 225 107.0855 206035.2 41 112.1122 25797.5 5 116.107 366628.9 74 117.0698 461334.1 93 119.0855 1465347 298 130.1226 475395.2 96 131.0852 82567.7 16 132.0933 1716232.7 349 145.1011 83250.2 16 146.1088 20110.1 4 147.1168 4906735.8 999 159.1167 33882.1 6 161.1324 132570.1 26 //