DEOXYNIVALENOL structure
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Common Name | DEOXYNIVALENOL | ||
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CAS Number | 51481-10-8 | Molecular Weight | 296.316 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 543.9±50.0 °C at 760 mmHg | |
Molecular Formula | C15H20O6 | Melting Point | 151-153ºC | |
MSDS | Chinese USA | Flash Point | 206.9±23.6 °C | |
Symbol |
GHS06 |
Signal Word | Danger |
Use of DEOXYNIVALENOLDeoxynivalenol, a mycotoxin of the trichothecenes family, crosses the intestinal mucosa by a paracellular pathway through the tight junctions. The Deoxynivalenol transport is not affected by P-glycoprotein (PgP) or multidrug resistance-associated proteins (MRPs) inhibitors[1]. |
Name | Deoxynivalenol |
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Synonym | More Synonyms |
Description | Deoxynivalenol, a mycotoxin of the trichothecenes family, crosses the intestinal mucosa by a paracellular pathway through the tight junctions. The Deoxynivalenol transport is not affected by P-glycoprotein (PgP) or multidrug resistance-associated proteins (MRPs) inhibitors[1]. |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 543.9±50.0 °C at 760 mmHg |
Melting Point | 151-153ºC |
Molecular Formula | C15H20O6 |
Molecular Weight | 296.316 |
Flash Point | 206.9±23.6 °C |
Exact Mass | 296.125977 |
PSA | 99.52000 |
LogP | -1.41 |
Vapour Pressure | 0.0±3.3 mmHg at 25°C |
Index of Refraction | 1.632 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS06 |
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Signal Word | Danger |
Hazard Statements | H300 |
Supplemental HS | Repeated exposure may cause skin dryness or cracking. |
Precautionary Statements | P264-P301 + P310 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T,Xn,F,Xi |
Risk Phrases | 25-68/20/21/22-67-66-36-20/21/22-11-36/37/38 |
Safety Phrases | 36/37/39-45-36-26-16-36/37-37/39 |
RIDADR | UN 2811 6.1/PG 2 |
WGK Germany | 3 |
RTECS | YD0167000 |
Packaging Group | I |
Hazard Class | 6.1(a) |
HS Code | 29329990 |
~80% DEOXYNIVALENOL CAS#:51481-10-8 |
Literature: Grove, John Frederick; McAlees, Alan J.; Taylor, Alan Journal of Organic Chemistry, 1988 , vol. 53, # 16 p. 3860 - 3862 |
~98% DEOXYNIVALENOL CAS#:51481-10-8 |
Literature: Cameron; Colvin 1989 , # 5 p. 887 - 895 |
Low toxicity of deoxynivalenol-3-glucoside in microbial cells.
Toxins (Basel.) 7(1) , 187-200, (2015) Host plants excrete a glucosylation enzyme onto the plant surface that changes mycotoxins derived from fungal secondary metabolites to glucosylated products. Deoxynivalenol-3-glucoside (DON3G) is synt... |
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Deoxynivalenol-mimic nanobody isolated from a naïve phage display nanobody library and its application in immunoassay.
Anal. Chim. Acta 887 , 201-8, (2015) In this study, using mycotoxin deoxynivalenol (DON) as a model hapten, we developed a nanobody-based environmental friendly immunoassay for sensitive detection of DON. Two nanobodies (N-28 and N-31) w... |
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Neurological sequelae induced by alphavirus infection of the CNS are attenuated by treatment with the glutamine antagonist 6-diazo-5-oxo-l-norleucine.
J. Neurovirol. 21(2) , 159-73, (2015) Recovery from encephalomyelitis induced by infection with mosquito-borne alphaviruses is associated with a high risk of lifelong debilitating neurological deficits. Infection of mice with the prototyp... |
(3β,7α)-3,7,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one |
(3beta,7alpha,12R)-3,7,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one |
4-Desoxynivalenol |
Desoxynivalenol |
MFCD09039270 |
Vomitoxin |
Trichothec-9-en-8-one, 12,13-epoxy-3,7,15-trihydroxy-, (2α,3α,6β,7β,11β,12α)- |
Deoxynivalenol |
Trichothec-9-en-8-one, 12,13-epoxy-3,7,15-trihydroxy-, (3α,7α)- |
4-Deoxynivalenol |