MassBank Record: AC000115



 3,15-diacetyldeoxynivalenol; LC-ESI-ITFT; MS2; CE=10; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: AC000115
RECORD_TITLE: 3,15-diacetyldeoxynivalenol; LC-ESI-ITFT; MS2; CE=10; R=17500; [M+H]+
DATE: 2017.07.07
AUTHORS: Justin B. Renaud, J. David Miller, Mark W. Sumarah, Agriculture and Agri-Food Canada
LICENSE: CC BY-SA
COPYRIGHT: Copyright (C) 2017
PUBLICATION: Renaud, Justin B., and Mark W. Sumarah. Analytical and bioanalytical chemistry 408.12 (2016): 3083-3091.
COMMENT: CONFIDENCE isolated standard

CH$NAME: 3,15-diacetyldeoxynivalenol CH$NAME: 3,15-Bis(acetyloxy)-12,13-epoxy-7-hydroxytrichothec-9-en-8-one (3alpha)- CH$COMPOUND_CLASS: Natural Product; Fungal metabolite CH$FORMULA: C19H24O8 CH$EXACT_MASS: 380.1471 CH$SMILES: CC1=C[C@@H]2[C@](C(C1=O)O)([C@]3(C[C@H]([C@H]([C@@]34CO4)O2)OC(=O)C)C)COC(=O)C CH$IUPAC: InChI=1S/C19H24O8/c1-9-5-13-18(7-24-10(2)20,15(23)14(9)22)17(4)6-12(26-11(3)21)16(27-13)19(17)8-25-19/h5,12-13,15-16,23H,6-8H2,1-4H3/t12-,13-,15?,16-,17-,18-,19+/m1/s1 CH$LINK INCHIKEY: RANGFOQREJPKIH-QZQWDYNDSA-N CH$LINK: CAS 99604-10-1 CH$LINK: PUBCHEM CID:21120844
AC$INSTRUMENT: Q-Exactive Orbitrap Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-ITFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: IONIZATION_VOLTAGE 3.9 kV AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD AC$MASS_SPECTROMETRY: COLLISION_ENERGY 10 AC$MASS_SPECTROMETRY: RESOLUTION 17500 AC$CHROMATOGRAPHY: COLUMN_NAME Agilent RRHD Eclipse 50 x 2 mm, 1.8 uM AC$CHROMATOGRAPHY: FLOW GRADIENT 00:0 at 0 min, 100:0 at 0.5 min, 0:100 at 3.5 min, 0:100 at 5.5 min, 100:0 at 7 min AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL min-1 AC$CHROMATOGRAPHY: RETENTION_TIME 3.22 AC$CHROMATOGRAPHY: NAPS_RTI 860 AC$CHROMATOGRAPHY: Solvent A H2O 0.1% FA AC$CHROMATOGRAPHY: Solvent B ACN 0.1% FA
MS$FOCUSED_ION: BASE_PEAK 381.1526 MS$FOCUSED_ION: PRECURSOR_M/Z 381.1538 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE based on Fragment ion formula determination MS$DATA_PROCESSING: DEPROFILE Proteowizard
PK$SPLASH: splash10-001i-0296000000-42402aa280bf27a6f93a PK$ANNOTATION: m/z tentative_formula mass error(ppm) 109.0647 C7H9O1+ -0.9 125.0593 C7H9O2+ -3.26 133.0643 C9H9O1+ -3.74 137.0592 C8H9O2+ -3.71 173.0953 C12H13O1+ -4.63 187.1109 C13H15O1+ -4.56 189.0902 C12H13O2+ -4.29 197.0952 C14H13O1+ -4.58 203.1057 C13H15O2+ -4.75 213.09 C14H13O2+ -4.75 215.1058 C14H15O2+ -4.02 225.0899 C15H13O2+ -4.94 231.1006 C14H15O3+ -4.21 243.1005 C15H15O3+ -4.42 261.111 C15H17O4+ -4.35 273.1108 C16H17O4+ -4.89 279.1215 C15H19O5+ -4.29 303.1213 C17H19O5+ -4.61 321.132 C17H21O6+ -3.92 381.1526 C19H25O8+ -4.68 PK$NUM_PEAK: 20 PK$PEAK: m/z int. rel.int. 109.0648 308236.75 40 125.0597 703404.25 94 133.0648 294569.84375 39 137.0597 1207844.125 163 173.0961 263544.0625 34 187.1118 242545.515625 32 189.091 300158.09375 39 197.0961 242545.03125 32 203.1067 586568.625 78 213.091 1144651.0 154 215.1067 1053233.5 142 225.091 247232.0 32 231.1016 3469623.25 471 243.1016 1537732.375 208 261.1121 1197645.75 162 273.1121 381382.71875 50 279.1227 2051445.125 278 303.1227 353839.28125 47 321.1333 907140.75 122 381.1544 7346065.0 999 //