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CAS No 51481-10-8 , Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-

  • Name: Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-
  • Synonyms: Deoxynivalenol; Vomitoxin;Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-; 4-Deoxynivalenol; NSC 269144;Spiro[2,5-methano-1-benzoxepin-10,2'-oxirane],trichothec-9-en-8-one deriv.; 4-Desoxynivalenol; DON;Dehydronivalenol;
  • CAS Registry Number:
  • Transport: UN 2811 6.1/PG 2
  • Melting Point: 151-153 C
  • Flash Point: 206.9°C
  • Boiling Point: 543.9°Cat760mmHg
  • Density: 1.48g/cm3
  • Refractive index: 1.632
  • Safety Statements: 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.
  • Hazard Symbols: T,Xn,F,Xi
  • Flash Point: 206.9°C
  • Molecular Weight: 296.35
  • InChI: InChI=1/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15-/m1/s1
  • Risk Statements: 25-68/20/21/22-67-66-36-20/21/22-11-36/37/38
  • Molecular Formula: C15H20 O6
  • Molecular Structure:CAS No:51481-10-8 Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-

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51481-10-8 Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-

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51481-10-8 Deoxynivalenol

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51481-10-8 DEOXYNIVALENOL

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References of Trichothec-9-en-8-one,12,13-epoxy-3,7,15-trihydroxy-, (3a,7a)-
Title: Vomitoxin
CAS Registry Number: 51481-10-8
CAS Name: 12,13-Epoxy-3,7,15-trihydroxytrichothec-9-en-8-one
Synonyms: deoxynivalenol; dehydronivalenol
Molecular Formula: C15H20O6
Molecular Weight: 296.32
Percent Composition: C 60.80%, H 6.80%, O 32.40%
Literature References: Isoln of the trichothecene mycotoxin from Fusarium roseum and structure: N. Morooka et al., J. Food Hyg. Soc. Japan 13, 368 (1972); T. Yoshizawa, N. Morooka, Agric. Biol. Chem. 37, 2933 (1973). Isoln from F. graminearum: R. F. Vesonder et al., Appl. Microbiol. 26, 1008 (1973); eidem, Appl. Environ. Microbiol. 31, 280 (1976). Emetic and refusal activity in swine: D. M. Forsyth et al., ibid. 34, 547 (1977). HPLC analysis: G. A. Bennett et al., J. Am. Oil Chem. Soc. 58, 1002A (1981). Implicated as a chemical warfare agent with nivalenol, q.v. in Southeast Asia: N. Wade, Science 214, 34 (1981).
Properties: Fine needles from ethyl acetate + petr ether, mp 151-153°. [a]D25+6.35° (c = 0.07 in ethanol). uv max (ethanol): 218 nm (e 4500). LD50 i.p. in male, female mice (mg/kg): 70.0, 76.7 (Yoshizawa, Morooka).
Melting point: mp 151-153°
Optical Rotation: [a]D25+6.35° (c = 0.07 in ethanol)
Absorption maximum: uv max (ethanol): 218 nm (e 4500)
Toxicity data: LD50 i.p. in male, female mice (mg/kg): 70.0, 76.7 (Yoshizawa, Morooka)