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51481-10-8

Basic Information
CAS No.: 51481-10-8
Name: DEOXYNIVALENOL
Article Data: 8
Molecular Structure:
Molecular Structure of 51481-10-8 (DEOXYNIVALENOL)
Formula: C15H20 O6
Molecular Weight: 296.32
Synonyms: Spiro[2,5-methano-1-benzoxepin-10,2'-oxirane],trichothec-9-en-8-one deriv.; 4-Deoxynivalenol; 4-Desoxynivalenol; DON;Dehydronivalenol; Deoxynivalenol; NSC 269144; Vomitoxin
EINECS: 200-835-2
Density: 1.48g/cm3
Melting Point: 151-153 C
Boiling Point: 543.9°Cat760mmHg
Flash Point: 206.9°C
Hazard Symbols: T,Xn,F,Xi
Risk Codes: R25; R68/20/21/22; R67; R66; R36; R20/21/22; R11; R36/37/38
Safety: Poison by ingestion, subcutaneous, and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. A skin irritant. When heated to decomposition it emits acrid smoke and fumes.
PSA: 99.52000
LogP: -0.83770
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Chemistry

CBNumber: CB0391546
Chemical Name: (3α,7α)-3,7,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
Other names: DEOXYNIVALENO;Vomitoxin;DON;DEOXYNIVALENOL;3ALPHA,7ALPHA,15-TRIHYDROXY-12,13-EPOXYTRICHOTHEC-9-EN-8-ONE;VOMITOXIN;12,13-epoxy-3,7,15-trihydroxy-,(3-alpha,7-alpha)-trichothec-9-en-8-on;12,13-epoxy-3-alpha,7-alpha,15-trihydroxy-9-trichothecen-8-one;4-deoxynivalenol;dehydronivalenol;desoxynivalenol;rdtoxin;Spiro[2,5-methano-1-benzoxepin-10,2'-oxirane], trichothec-9-en-8-one deriv.;Trichothec-9-en-8-one, 12,13-epoxy-3,7,15-trihydroxy-, (3alpha,7alpha)-;DEOXYNIVALENOL,1X1ML, ETOAC/MEOH(95:5),2 00UG/ML;deoxynivalenol solution;TRICHOTHECENEVOMITOXIN;DEOXYNIVALENOL SOLUTION (100ΜG/ML ACETONITORILE SOLUTION);Deoxynivalenol, Vomitoxin;3α,7α,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one
MF: C15H20O6
FW: 296.32
Melting Point:151-153°C
Flash Point: -3 °C
Storage temp.: 2-8°C

Vomitoxin is a type B trichothecene, an epoxy-sesquiterpeneoid. Vomitoxin occurs predominantly in grains such as wheat, barley, oats, rye, and maize, and less often in rice, sorghum, and triticale.

Toxicity Data With Reference

1.   

skn-gpg 148 μg MLD

   FAATDF    Fundamental and Applied Toxicology. 4 (2, Pt 2),(1984),S124.
2.   

orl-mus LD50:46 mg/kg

   FAATDF    Fundamental and Applied Toxicology. 4 (2, Pt 2),(1984),S124.
3.   

ipr-mus LD50:43 mg/kg

   TOXIA6    Toxicon. 24 (1986),985.
4.   

scu-mus LD50:45 mg/kg

   TOXIA6    Toxicon. 24 (1986),985.
5.   

scu-dog LD50:27 mg/kg

   VHTODE    Veterinary and Human Toxicology. 25 (1983),335.

 

Safety Profile

Poison by ingestion, subcutaneous, and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. A skin irritant. When heated to decomposition it emits acrid smoke and fumes.

Human:  1 ppm  restriction of vomitoxin.
Companion animals: 5 ppm  restriction of vomitoxin.The grains is not exceed 40% of the diet.
Livestock and farm animals: 10 ppm  restriction of vomitoxin.Ingredients may not exceed 50% of the diet.
Dairy cow :2 ppm  restriction of vomitoxin

Specification

vomitoxin appears to occur through the central nervous system. Vomitoxin is strong protein inhibitors. vomitoxin causes the brain to increase its uptake of the amino acid tryptophan and, in turn, its synthesis of serotonin. Increased levels of serotonin are believed to be responsible for the anorexic effects of DON and other tricothecenes. Irritation of the gastrointestinal tract may also play a role in reducing feed intake... This fact may also partially explain the high incidence of pars esaughageal stomach ulcers observed in sows off feed during feed refusal.