MassBank Record: AC000233



 T-2 Toxin; 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: AC000233
RECORD_TITLE: T-2 Toxin; LC-ESI-ITFT; MS2; CE=10; R=17500; [M+H]+
DATE: 2017.07.07
AUTHORS: Justin B. Renaud, 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 commercial standard

CH$NAME: T-2 Toxin CH$NAME: Fusariotoxin T 2; Insariotoxin; T-2 mycotoxin CH$NAME: (2alpha,3alpha,4beta,8alpha)-4,15-bis(acetyloxy)-3-hydroxy-12,13-epoxytrichothec-9-en-8-yl 3-methylbutanoate CH$COMPOUND_CLASS: Natural Product; Fungal metabolite CH$FORMULA: C24H34O9 CH$EXACT_MASS: 466.22027 CH$SMILES: CC1=C[C@@H]2[C@](C[C@@H]1OC(=O)CC(C)C)([C@]3([C@@H]([C@H]([C@H]([C@@]34CO4)O2)O)OC(=O)C)C)COC(=O)C CH$IUPAC: InChI=1S/C24H34O9/c1-12(2)7-18(27)32-16-9-23(10-29-14(4)25)17(8-13(16)3)33-21-19(28)20(31-15(5)26)22(23,6)24(21)11-30-24/h8,12,16-17,19-21,28H,7,9-11H2,1-6H3/t16-,17+,19+,20+,21+,22+,23+,24-/m0/s1 CH$LINK INCHIKEY: BXFOFFBJRFZBQZ-QYWOHJEZSA-N CH$LINK: CAS 21259-20-1 CH$LINK: PUBCHEM CID:5284461 CH$LINK: CHEMSPIDER 58828722 CH$LINK: KNAPSACK C00003192
AC$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 3.54 AC$CHROMATOGRAPHY: NAPS_RTI 1035 AC$CHROMATOGRAPHY: Solvent A H2O 0.1% FA AC$CHROMATOGRAPHY: Solvent B ACN 0.1% FA
MS$FOCUSED_ION: BASE_PEAK 467.226 MS$FOCUSED_ION: PRECURSOR_M/Z 467.227 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE based on Fragment ion formula determination MS$DATA_PROCESSING: DEPROFILE Proteowizard
PK$SPLASH: splash10-066r-0495700000-b7157edfa998d0c7009f PK$ANNOTATION: m/z tentative_formula mass error(ppm) 57.0707 85.0652 C5H9O1+ 4.73 105.0698 C8H9+ -0.84 121.0645 C8H9O1+ -2.46 125.0593 C7H9O2+ -3.26 157.1002 C12H13+ -6.31 169.1005 C13H13+ -4.09 173.0952 C12H13O1+ -5.21 185.0953 C13H13O1+ -4.33 187.1107 C13H15O1+ -5.63 197.0954 C14H13O1+ -3.56 199.1111 C14H15O1+ -3.28 203.1058 C13H15O2+ -4.25 215.106 C14H15O2+ -3.09 217.1214 C14H17O2+ -4.22 227.1058 C15H15O2+ -3.8 233.1164 C14H17O3+ -3.54 245.1163 C15H17O3+ -3.78 257.1164 C16H17O3+ -3.21 263.1267 C15H19O4+ -4.13 275.1267 C16H19O4+ -3.95 287.1267 C17H19O4+ -3.79 305.1372 C17H21O5+ -3.77 323.1476 C17H23O6+ -4.06 347.1473 C19H23O6+ -4.64 347.1854 C20H27O5+ 0.27 365.1578 C19H25O7+ -4.58 389.1949 C22H29O6+ -2.49 407.2049 C22H31O7+ -3.76 425.2167 C22H33O8+ -0.69 449.2153 C24H33O8+ -3.77 467.226 C24H35O9+ -3.33 PK$NUM_PEAK: 32 PK$PEAK: m/z int. rel.int. 57.0707 35333.1484375 32 85.0648 126290.640625 120 105.0699 71413.8515625 67 121.0648 78119.78125 73 125.0597 35537.79296875 33 157.1012 40131.76953125 37 169.1012 69084.03125 65 173.0961 54750.58984375 51 185.0961 164879.046875 157 187.1118 54455.65625 51 197.0961 178388.359375 170 199.1118 104065.8828125 98 203.1067 67889.1953125 64 215.1067 317463.75 303 217.1223 101161.1171875 96 227.1067 236587.234375 225 233.1172 87801.984375 83 245.1172 475680.21875 455 257.1172 88282.171875 83 263.1278 185931.046875 177 275.1278 77829.59375 73 287.1278 187495.265625 178 305.1384 637078.6875 610 323.1489 107140.8046875 101 347.1489 59725.484375 56 347.1853 45162.53125 42 365.1595 299520.28125 286 389.1959 58256.48828125 54 407.2064 215072.34375 205 425.217 47032.7578125 44 449.217 244118.21875 233 467.2276 1042317.625 999 //