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Merck
CN

90187

T-2 Toxin

≥98.0% (TLC)

Synonym(s):

12,13-Epoxytrichothec-9-ene-3,4,8,15-tetrol-4,15-diacetate-8-isovalerate, 4β,15-Diacetoxy-3α-hydroxy-8α-(3-methylbutyryloxy)-12,13-epoxytrichothec-9-ene

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About This Item

Empirical Formula (Hill Notation):
C24H34O9
CAS Number:
21259-20-1
Molecular Weight:
466.52
EC Number:
244-297-7
UNSPSC Code:
12352200
PubChem Substance ID:
329769858
Beilstein/REAXYS Number:
3575695
MDL number:
MFCD00871255

Key Documents

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InChI key

BXFOFFBJRFZBQZ-QYWOHJEZSA-N

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

SMILES string

[H][C@]12O[C@]3([H])[C@H](O)[C@@H](OC(C)=O)[C@](C)([C@@]1(COC(C)=O)C[C@H](OC(=O)CC(C)C)C(C)=C2)[C@]34CO4

assay

≥98.0% (TLC)

form

powder

Other Notes

Reference in the quantitative determination of trichothecenes

Disclaimer

mycotoxin; severe poison

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Skin Irrit. 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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R. Schmidt et al.
Zeitschrift fur Lebensmittel-Untersuchung Und -Forschung, 175, 169-169 (1982)
Fresenius Journal of Analytical Chemistry, 317, 665-665 (1984)
High-performance liquid chromatography of trichothecenes. I. Detection of T-2 toxin and HT-2 toxin.
R Schmidt et al.
Journal of chromatography, 212(3), 370-373 (1981-08-07)
Soujanya Ratna Edupuganti et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 923-924, 98-101 (2013-03-19)
An affinity purification method that isolates T-2 toxin-specific IgY utilizing a T-2-toxin-immobilized column was developed. The T-2 toxin was covalently coupled via a carbonyldiimidazole-activated hydroxyl functional group to amine-activated sepharose beads. The affinity-purified IgY was characterized by gel electrophoresis, fast
Yanshen Li et al.
Journal of agricultural and food chemistry, 59(8), 3441-3453 (2011-03-23)
This review focuses on the toxicity and metabolism of T-2 toxin and analytical methods used for the determination of T-2 toxin. Among the naturally occurring trichothecenes in food and feed, T-2 toxin is a cytotoxic fungal secondary metabolite produced by
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