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Oxendolone

CAS No.
33765-68-3
Chemical Name:
Oxendolone
Synonyms
TSAA 291;Roxenone;Prostetin;Oxendolone;ESTR-4-EN-3-ONE;Oxendolone USP/EP/BP;16b-Ethyl-19-nortestosterone;16β-Ethyl-19-nortestosterone;16beta-Ethyl-19-nortestosterone;16β-Ethyl-17β-hydroxyestr-4-en-3-one
CBNumber:
CB4969631
Molecular Formula:
C20H30O2
Molecular Weight:
302.455
MDL Number:
MFCD00864663
MOL File:
33765-68-3.mol
Last updated:2023-07-14 17:45:11

Oxendolone Properties

Melting point 152-153℃
alpha D +41° (c = 1.0 in ethanol)
Boiling point 383.47°C (rough estimate)
Density 1.0434 (rough estimate)
refractive index 1.4980 (estimate)
pka 15.08±0.60(Predicted)
FDA UNII MN4I850D4P

SAFETY

Risk and Safety Statements

Toxicity LD50 in rats, mice (g/kg): >10 orally; 5-10 i.m. and i.p. (Hiraga, 1971)

Oxendolone price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0012147 OXENDOLONE 95.00% 33765-68-3 5MG $495.1 2021-12-16 Buy
Medical Isotopes, Inc. 18733 Oxendolone 33765-68-3 25mg $1500 2021-12-16 Buy
Crysdot CD31002191 Oxendolone 95+% 33765-68-3 1g $1186 2021-12-16 Buy
Product number Packaging Price Buy
API0012147 5MG $495.1 Buy
18733 25mg $1500 Buy
CD31002191 1g $1186 Buy

Oxendolone Chemical Properties,Uses,Production

Description

Oxendolone can be used as an anti-androgen drug and has an anti-androgen effect. Competitive antagonism occurs directly with male hormones in the prostate, inhibiting the weight of the prostate and seminal vesicles. The specificity of its anti-androgen effect is high, and it directly competes with androgens in the prostate and hardly shows other hormonal effects.

?Acute toxicity

LD50 in rats and mice (g/kg): >10 orally; 5-10 intramuscular injection and intraperitoneal injection

Originator

Prostetin,Takeda, Japan ,1981

Uses

Oxendolone is used as an anti-androgen (benign prostatic hypertrophy).

Definition

ChEBI: Oxendolone is an organic molecular entity.

Manufacturing Process

To a solution of 3.0 g of 16β-ethylestra-4-ene-3,17-dione dissolved in 150 ml of dioxane, are added 15 g of ethyl orthoformate and 0.1 g of ptoluenesulfonic acid, followed by stirring for 2 hours at room temperature. The reaction solution is poured into 300 ml of a 5% aqueous solution of sodium hydrogen carbonate and the resultant mixture is extracted with ether. The ether layer is washed with water and dried, followed by evaporation of the solvent to give crude crystals of 3-ethoxy-16β-ethylestra-3,5-diene-17-one. The crystals are recrystallized from ether to give 3.0 g of the compound melting at 114°C to 115°C
To a solution of 3.0 g of the enol-ether compound obtained above in 50 ml of methanol, is added 1.5 g of sodium borohydride. After standing for 1.5 hours at room temperature, the reaction solution is poured into 300 ml of water. The resulting precipitates are collected by filtration and recrystallized from ether to give 2.8 g of 3-ethoxy-16β-ethylestra-3,5-dien-17β-ol melting at 131°C to 133°C.
To a solution of 2.5 g of 3-ethoxy-16β-ethylestra-3,5-diene-17β-ol dissolved in 50 ml of methanol is added 1.2 ml of concentrated hydrochloric acid, followed by stirring for 10 minutes. The reaction solution is poured into 250 ml of water. The precipitated crystals are collected by filtration and recrystallized from ether to give 2.3 g of 16β-ethyl-17β-hydroxyestra-4-en-one melting at 152°C to 153°C.

Therapeutic Function

Antiandrogen

Oxendolone Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9320 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58

View Lastest Price from Oxendolone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Oxendolone USP/EP/BP pictures 2021-06-08 Oxendolone USP/EP/BP
33765-68-3
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Oxendolone 16b-Ethyl-17b-hydroxyestr-4-en-3-one 16b-Ethyl-19-nortestosterone Estr-4-en-3-one, 16b-ethyl-17b-hydroxy- (8CI) Estr-4-en-3-one, 16-ethyl-17-hydroxy-, (16b,17b)- (9CI) TSAA 291 ESTR-4-EN-3-ONE 16β-Ethyl-17β-hydroxyestr-4-en-3-one 16β-Ethyl-19-nortestosterone 16beta-Ethyl-17beta-hydroxyestr-4-en-3-one 16beta-Ethyl-19-nortestosterone Prostetin Estr-4-en-3-one, 16-ethyl-17-hydroxy-, (16β,17β)- Oxendolone USP/EP/BP Roxenone 33765-68-3