脱氧雪腐镰刀菌烯醇（CAS 51481-10-8）：分子式 C15H20O6、分子量 296.31。
| CAS号 | 51481-10-8 |
|---|---|
| 分子式 | C15H20O6 |
| 分子量 | 296.31 |
| 熔点 | 151-153 °C |
| 沸点 | 500–550 °C |
| LogP | -0.7 |
| 应用领域 | Uses: A trichothecene mycotoxin、[Merck Index] Reportedly used as biological、chemical warfare agent、[HSDB] Zearalenone、deoxynivalenol、and fusarenon X are mycotoxins produced by 3 Fusarium species (F. graminearum、F. culmorum、and F. crookwellense) that grow on wheat、barley、and maize in humid conditions. [IARC] Common contaminant of barley、corn、rye、safflower seeds、wheat、and mixed feeds、[Reference #1]、During the late 1970s and early 1980s、there was use in northern Thailand、Kampuchea、Cambodia、and Laos as chemical warfare agents by Russian troops.、Trichothecenes、Since these toxins also kill plants、there have been suggestions to use them as mycoherbicides against drug crops in production countries... .、Unconfirmed and controversial findings suggest the use of trichothecenes、including 4-deoxynivalenol、as biological warfare agents...、Vomitoxin、also known as deoxynivalenol (DON)、is a type B trichothecene、an epoxy-sesquiterpeneoid. Trichothecenes are a very large family of chemically related mycotoxins produced by various species of Fusarium、Myrothecium、Trichoderma、Trichothecium、Cephalosporium、Verticimonosporium、and Stachybotrys. Vomitoxin occurs predominantly in grains such as wheat、oats、and maize、and less often in rice、sorghum、and triticale. The occurrence of deoxynivalenol is associated primarily with Fusarium graminearum (Gibberella zeae) and F. culmorum、both of which are important plant pathogens which cause Fusarium head blight in wheat and Gibberella ear rot in maize. (L1948、L1951)、Use Classification: Food Contaminant -> MYCOTOXIN -> JECFA Functional Classes、General Manufacturing Information: Implicated as a chemical warfare agent with nivalenol ... in Southeast Asia、Processing and milling studies have shown little reduction in deoxynivalenol (DON) levels from the cereal to the finished product. Similarly、baking is not effective in destroying DON. |
登记用途：Uses: A trichothecene mycotoxin、[Merck Index] Reportedly used as biological、chemical warfare agent、[HSDB] Zearalenone、deoxynivalenol、and fusarenon X are mycotoxins produced by 3 Fusarium species (F. graminearum、F. culmorum、and F. crookwellense) that grow on wheat、barley、and maize in humid conditions. [IARC] Common contaminant of barley、corn、rye、safflower seeds、wheat、and mixed feeds、[Reference #1]、During the late 1970s and early 1980s、there was use in northern Thailand、Kampuchea、Cambodia、and Laos as chemical warfare agents by Russian troops.、Trichothecenes、Since these toxins also kill plants、there have been suggestions to use them as mycoherbicides against drug crops in production countries... .、Unconfirmed and controversial findings suggest the use of trichothecenes、including 4-deoxynivalenol、as biological warfare agents...、Vomitoxin、also known as deoxynivalenol (DON)、is a type B trichothecene、an epoxy-sesquiterpeneoid. Trichothecenes are a very large family of chemically related mycotoxins produced by various species of Fusarium、Myrothecium、Trichoderma、Trichothecium、Cephalosporium、Verticimonosporium、and Stachybotrys. Vomitoxin occurs predominantly in grains such as wheat、oats、and maize、and less often in rice、sorghum、and triticale. The occurrence of deoxynivalenol is associated primarily with Fusarium graminearum (Gibberella zeae) and F. culmorum、both of which are important plant pathogens which cause Fusarium head blight in wheat and Gibberella ear rot in maize. (L1948、L1951)、Use Classification: Food Contaminant -> MYCOTOXIN -> JECFA Functional Classes、General Manufacturing Information: Implicated as a chemical warfare agent with nivalenol ... in Southeast Asia、Processing and milling studies have shown little reduction in deoxynivalenol (DON) levels from the cereal to the finished product. Similarly、baking is not effective in destroying DON.。
脱氧雪腐镰刀菌烯醇 是一种化工化合物，登记 CAS 号为 51481-10-8，分子式 C15H20O6（分子量 296.31）。
登记 CAS 号：51481-10-8
其分子式 C15H20O6 由 15 个碳、20 个氢、6 个氧 组成。
别名/同义词：脱氧雪腐镰刀菌烯醇 · DEOXYNIVALENOL
脱氧雪腐镰刀菌烯醇 的 CAS 登记号为 51481-10-8。
分子式 C15H20O6，分子量 296.31。
别名/同义词：脱氧雪腐镰刀菌烯醇、DEOXYNIVALENOL。
登记用途：Uses: A trichothecene mycotoxin、[Merck Index] Reportedly used as biological、chemical warfare agent、[HSDB] Zearalenone、deoxynivalenol、and fusarenon X are mycotoxins produced by 3 Fusarium species (F. graminearum、F. culmorum、and F. crookwellense) that grow on wheat、barley、and maize in humid conditions. [IARC] Common contaminant of barley、corn、rye、safflower seeds、wheat、and mixed feeds、[Reference #1]、During the late 1970s and early 1980s、there was use in northern Thailand、Kampuchea、Cambodia、and Laos as chemical warfare agents by Russian troops.、Trichothecenes、Since these toxins also kill plants、there have been suggestions to use them as mycoherbicides against drug crops in production countries... .、Unconfirmed and controversial findings suggest the use of trichothecenes、including 4-deoxynivalenol、as biological warfare agents...、Vomitoxin、also known as deoxynivalenol (DON)、is a type B trichothecene、an epoxy-sesquiterpeneoid. Trichothecenes are a very large family of chemically related mycotoxins produced by various species of Fusarium、Myrothecium、Trichoderma、Trichothecium、Cephalosporium、Verticimonosporium、and Stachybotrys. Vomitoxin occurs predominantly in grains such as wheat、oats、and maize、and less often in rice、sorghum、and triticale. The occurrence of deoxynivalenol is associated primarily with Fusarium graminearum (Gibberella zeae) and F. culmorum、both of which are important plant pathogens which cause Fusarium head blight in wheat and Gibberella ear rot in maize. (L1948、L1951)、Use Classification: Food Contaminant -> MYCOTOXIN -> JECFA Functional Classes、General Manufacturing Information: Implicated as a chemical warfare agent with nivalenol ... in Southeast Asia、Processing and milling studies have shown little reduction in deoxynivalenol (DON) levels from the cereal to the finished product. Similarly、baking is not effective in destroying DON.。
脱氧雪腐镰刀菌烯醇（CAS 51481-10-8）的独立参考数据，整理自公开化学数据库。
| CAS 号 | 51481-10-8 |
|---|---|
| PubChem CID | 40024 |
| 分子式 | C15H20O6 |
| IUPAC 名称 | (1R,2R,3S,7R,9R,10R,12S)-3,10-dihydroxy-2-(hydroxymethyl)-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4-one |
| UNII（FDA） | JT37HYP23V |
| Molecular Weight | 296.31 |
|---|---|
| XLogP3 | -0.7 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 1 |
| Exact Mass | 296.12598835 |
| Monoisotopic Mass | 296.12598835 |
| Topological Polar Surface Area | 99.5 |
| Heavy Atom Count | 21 |
| Boiling Point | 500–550 °C |
|---|---|
| Melting Point | 151-153 °C |
| Flash Point | 206.9 ± 2.5 °C |
| Collision Cross Section | 169.59 Ų [M+HCOO]- |
| Collision Cross Section | 171.51 Ų [M+Na]+ |
DEOXYNIVALENOL; 51481-10-8; 4-Deoxynivalenol; Dehydronivalenol; 4-Desoxynivalenol; Desoxynivalenol; CCRIS 7801; Rd toxin; NSC 269144; JT37HYP23V; 3alpha,7alpha,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one; CHEBI:10022; 12,13-Epoxy-3-alpha,7-alpha,15-trihydroxy-9-trichothecen-8-one; NSC-269144; Trichothec-9-en-8-one, 12,13-epoxy-3,7,15-trihydroxy-, (3-alpha,7-alpha)-; 3-epi-DON
| 法规与食品接触 | MYCOTOXIN: Food Contaminant TRS 959-JECFA 72 72nd_2011_Deoxynivalenol.pdf |
|---|
| 已通报的危害声明 | H300 (100%) |
|---|
脱氧雪腐镰刀菌烯醇 · CAS 51481-10-8 · C15H20O6. UNII JT37HYP23V. Boiling Point: 500–550 °C; Melting Point: 151-153 °C; Flash Point: 206.9 ± 2.5 °C.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: DEOXYNIVALENOL