| Source: | HT2 by Fermentek is semi synthetic. It is chemically derived from
T2 toxin from Fusarium tricinctum
|
| Synonyms |
Trichothec-9-ene-3alpha,4beta,8alpha,15-tetrol, 12,13-epoxy-,
15-acetate 8-isovalerate |
| Description: | HT2 Toxin: A trichothecene group mycotoxin. |
| CAS number: | 26934-87-2 |
| Merck index: | |
| Molecular weight: | 424.48 |
| Structure: | 
 |
| Molecular Formula: |
C22H32O8 |
| Canonical SMILES: |
CC1=CC2C(CC1OC(=O)CC(C)C)(C3(C(C(C(C34CO4)O2)O)O)C)COC(=O)C |
Solubility
information: | Dichloromethane, DMSO, Ethanol, Ethyl Acetate. Slightly soluble in petroleum ether; very slightly soluble in water. |
| Specifications | |
| Appearance: | White solid. |
| Purity: | At least 98% by TLC, HPLC |
| λmax: | |
| Melting point | 151°C-152°C |
| Solubility | Clear colorless solution at 5 mg/ml of Dichloromethane. |
| Storage | -20°C |
| Applications | |
| Warnings | TOXIC. Highly irritating to skin and mucous nembranes. Direct contact may cause extensive inflammation and tissue necrosis. May be lethal. |
| Classification | trichothecene
mycotoxin |
| Related products |
T2 toxin , Vomitoxin (deoxynivalenol) , deacetoxyscirpenol,
|
| | For Research use only. Not for Human or Drug use
GMP/API grade available on request
No genetically modified organisms are used. |
| Publications | |
| | Yoshizawa T, Kohno H, Ikeda K, Shinoda T, Yokohama H, Morita K, Kusada O, Kobayashi Y.
A practical method for measuring deoxynivalenol, nivalenol, and T-2 + HT-2 toxin in foods by an enzyme-linked immunosorbent assay using monoclonal antibodies.
Biosci Biotechnol Biochem. 2004 Oct;68(10):2076-85. |
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