标准品 3-乙酰基脱氧雪腐镰刀菌烯醇/3-Acetyl Deoxynivale...
- 型号:标准品
- 产地:Fermentek
- 供应商:广州市齐云生物技术有限公司
- 供应商报价:1500
- 标签:3-乙酰基脱氧雪腐镰刀菌烯醇/3-Acetyl Deoxynivalenol,1500,广州市齐云生物技术有限公司
3-乙酰基脱氧雪腐镰刀菌烯醇/3-Acetyl Deoxynivalenol
| Source: | Deoxynivalenol, 3-acetyl (3ADON) is derived from Fusarium graminearum. |
| Synonyms | 3α-Acetylvomitoxin 3-Acetyl don 3-Acetyldeoxynivalenol Dehydronivalenol monoacetate Deoxynivalenol monoacetate NSC 26703 |
| Description: | Natural, Type B trichothecene mycotoxin |
| CAS number: | 50722-38-8 |
| Merck index: | not listed |
| Molecular weight: | 338.4 |
| Structure: |
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| Molecular Formula: | C17H22O7 |
| Solubility information: | 3-acetyl Deoxynivalenol is soluble in common polar organic solvents as acetonitrile, methanol and ethyl acetate, only slightly soluble in water. Trichothecenes with acetoxy-groups are unstable in methanol, even when stored in a freezer [H. Pettersson, EU-Commission Progress Report SMT4-CT96-2047, 1-24, (1998), "Intercomparison of trichothecene analysis and feasibility to produce certified calibrants and reference material"] Acetonitrile is recommended as solvent for 3-acetyl Deoxynivalenol as it has no significant UV absorbance below 220 nm. |
| Specifications | |
| Appearance: | White crystalline solid. |
| Purity: | At least 98% by TLC |
| λmax: | |
| Melting point | 185°C-187°C |
| Solubility | CLEAR COLORLESS SOLUTION AT 20 MG/ML IN ETHANOL CLEAR COLORLESS SOLUTION AT 20 MG/ML IN Acetonitrile |
| Storage | Store as supplied, at 4°C. |
| Classification | trichothecene mycotoxin |
| Applications | |
| Warnings | Toxicmycotoxin. |
| Classification | trichothecene mycotoxin |
| Related products | Zearalenone Fumonisin_B1 Deoxynivalenol |
| For Research use only. Not for Human or Drug use GMP/API grade available on request No genetically modified organisms are used. | |
| Publications | |
| Bretz M, Beyer M, Cramer B, Humpf HU. Stable isotope dilution analysis of the Fusarium mycotoxins Vomitoxin (deoxynivalenol) (DON) and 3-acetyl Vomitoxin (deoxynivalenol) (DON) . Mol Nutr Food Res. 2006 Mar;50(3):251-60 |
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