所有图片(1)
别名:
3α,4β,7α, 15-T四羟基-12,13-环氧单端孢霉-9-烯-8-酮, NIV
经验公式（希尔记法）:
C15H20O7
CAS号:
分子量:
312.32
EC 号:
MDL编号:
UNSPSC代码:
85151701
PubChem化学物质编号:
NACRES:
NA.24
推荐产品
等级
analytical standard
质量水平
保质期
limited shelf life, expiry date on the label
浓度
100 μg/mL in acetonitrile
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
cleaning products
cosmetics
food and beverages
personal care
格式
single component solution
储存温度
−20°C
SMILES字符串
[H][C@]12O[C@]3([H])[C@H](O)[C@@H](O)[C@@](C)([C@]34CO4)[C@@]1(CO)[C@H](O)C(=O)C(C)=C2
InChI
1S/C15H20O7/c1-6-3-7-14(4-16,11(20)8(6)17)13(2)10(19)9(18)12(22-7)15(13)5-21-15/h3,7,9-12,16,18-20H,4-5H2,1-2H3/t7-,9-,10-,11-,12-,13-,14-,15+/m1/s1
InChI key
UKOTXHQERFPCBU-XBXCNEFVSA-N
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一般描述
Certan 样品瓶
瓜萎镰菌醇是由雪腐镰刀菌（Fusarium nivale）产生的潜在的单端孢霉烯真菌毒素。已通过碱性单细胞凝胶电泳分析评估了瓜萎镰菌醇的遗传毒性。
瓜萎镰菌醇是由镰刀菌属产生的次生代谢产物，镰刀菌属是小麦和其他谷物的植物病原性真菌。
瓜萎镰菌醇是由镰刀菌属产生的次生代谢产物，镰刀菌属是小麦和其他谷物的植物病原性真菌。
应用
有关合适仪器技术的更多信息，请参考产品分析证书。如需进一步支持，请联系技术服务。
瓜萎镰菌醇被用作标准品，研究脱氧萎镰菌醇和瓜萎镰菌醇在体外通过吸附材料（活性炭）与霉菌毒素的结合。
警示用语：
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
WGK
WGK 2
闪点(°F)
35.6 °F
闪点(°C)
2 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
高风险级别生物产品--毒素类产品
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Removal of toxic metals and toxins using microbial biomass has been introduced as an inexpensive, new promising method on top of conventional methods for decontamination of food, raw material and concentrated. In this article the potential application of lactic acid
S Tsuda et al.
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Applied and environmental microbiology, 78(7), 2161-2167 (2012-01-31)
Fusarium graminearum (Gibberella zeae) is an important pathogen of wheat, maize, barley, and rice in South Korea, and harvested grain often is contaminated with trichothecenes such as deoxynivalenol and nivalenol. In this study, we examined 568 isolates of F. graminearum
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Type B trichothecenes, deoxynivalenol (DON) and nivalenol (NIV), are secondary metabolites of Fusarium species and are major pollutants in food and feed products. Recently, the production trend of their derivatives, 3-acetyldeoxynivalenol (3-AcDON), 15-acetyldeoxynivalenol (15-AcDON), and 4-acetylnivalenol (4-AcNIV or fusarenon-X), has
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