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Azacosterol dihydrochloride

CAS No.
1249-84-9
Chemical Name:
Azacosterol dihydrochloride
Synonyms
Azacosterol;Azocosterol;Azocosterol 2HCl;Azacosterol dihydrochloride;Androst-5-en-3-ol, 17-[[3-(dimethylamino)propyl]methylamino]-, hydrochloride (1:2), (3β,17β)-
CBNumber:
CB51178066
Molecular Formula:
C25H45ClN2O
Molecular Weight:
425.1
MDL Number:
MOL File:
1249-84-9.mol
MSDS File:
SDS
Last updated:2024-12-18 14:08:57

Azacosterol dihydrochloride Properties

alpha D -32°
FDA UNII B32804UAUQ
EPA Substance Registry System Azacosterol hydrochloride (1249-84-9)

SAFETY

Risk and Safety Statements

Toxicity LD50 orl-rat: 470 mg/kg 85ARAE 3,100,76/77

Azacosterol dihydrochloride price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biorbyt Ltd orb146177 Azocosterol 2HCL >99% 1249-84-9 100mg $606.9 2021-12-16 Buy
Biorbyt Ltd orb146177 Azocosterol 2HCL >99% 1249-84-9 250mg $912.9 2021-12-16 Buy
Biorbyt Ltd orb146177 Azocosterol 2HCL >99% 1249-84-9 1g $1802 2021-12-16 Buy
DC Chemicals DC4141 Azocosterol2HCL 99% 1249-84-9 100mg $300 2021-12-16 Buy
DC Chemicals DC4141 Azocosterol2HCL 99% 1249-84-9 250mg $600 2021-12-16 Buy
Product number Packaging Price Buy
orb146177 100mg $606.9 Buy
orb146177 250mg $912.9 Buy
orb146177 1g $1802 Buy
DC4141 100mg $300 Buy
DC4141 250mg $600 Buy

Azacosterol dihydrochloride Chemical Properties,Uses,Production

Description

Azacosterol hydrochloride is a diaza derivative of cholesterol which acts as a hypocholesteremic agent by blocking delta-24-reductase causing accumulation of desmosterol.

Originator

Ornitrol,Avitrol Corporation

Uses

Chemosterilant, avian.

Manufacturing Process

A solution of 15 parts of 3β-hydroxyandrost-5-en-17-one and 30 parts of 3- dimethylaminopropylamine in 36.6 parts of formic acid is heated in an oil bath at about 170-180°C for about 24 hours. The cooled mixture is diluted with about 500 parts of water, and the resulting aqueous mixture is extracted with chloroform, containing a small amount of methanol. The organic layer is separated, washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure. The viscous residue is dissolved in a mixture of 80 parts of isopropyl alcohol and 420 parts of ether, and this solution is treated with isopropanolic hydrogen chloride. The resulting precipitate is collected by filtration and washed with acetone to afford 17β-[N- (3-dimethylaminopropyl)formamido-1-androst-5-en-3β-ol hydrochloride. A solution of this hydrochloride in aqueous methanol is made alkaline by the addition of dilute aqueous sodium hydroxide, and the resulting colloidal precipitate is extracted with chloroform. The chloroform extracts washed with water, dried over anhydrous sodium sulfate and concentrated to dryness to afford a residue, which is crystallized from acetone, resulting in 17β-[N-(3- dimethylaminopropyl)formamido]androst-5-en-3β-ol, which displays a double melting point at about 116-118°C and 143-148°C, [α]D= -67.5° (chloroform).
To a slurry of 4 parts of LiAlH4 in 150 parts of dioxane is added dropwise with stirring, at the reflux temperature a solution of 10 parts of 17β-[N-(3- dimethylaminopropyl) formamido]androst-5-en-3β-ol in 150 parts of dioxane. This reaction mixture is heated at reflux for about 18 hours longer, and then treated dropwise successively, at the reflux temperature, with a solution of 4 parts of water in 25 parts of dioxane, 3 parts of 20% aqueous sodium hydroxide, and 14 parts of water. The resulting mixture is clarified by filtration, and the residue on the filter is washed with fresh dioxane. The filtrates are combined, evaporated to dryness under reduced pressure, and the resulting residue is recrystallized from acetone-methanol to produce 17β-[N-methyl-N-(3- dimethylaminopropyl)amino]androst-5-en-3β-ol, M.P. about 146-148°C, [α]D= -54.5° (chloroform). A solution of this amine in ether-isopropyl alcohol is treated with isopropanolic hydrogen chloride to afford Azacosterol dihydrochloride, [α]D= -32° (methanol).

Therapeutic Function

Hypocholesteremic

Safety Profile

Poison by ingestion andintraperitoneal routes. Experimental reproductive effects.Mutation data reported. When heated to decomposition itemits toxic fumes of NOx and HCl.

Azacosterol dihydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Azacosterol dihydrochloride Suppliers

Global( 15)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-81148696 +86-15536356810 1022@dideu.com China 3882 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30239 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43340 58
TargetMol Chemicals Inc.
+8613564774135 zijue.cai@tsbiochem.com United States 19885 58
Chengdu HuaXia Chemical Reagent Co. Ltd 400-1166-196 13458535857 cdhxsj@163.com China 13350 58
AN PharmaTech Co Ltd 86(21)68097365 sales@anpharma.net China 4891 55
Shandong Xiya Chemical Co., Ltd. 4009903999 13395398332 sales@xiyashiji.com China 20806 60
Shandong Ono Chemical Co., Ltd. 0539-6362799 20) China 9998 58
Aishilun biotechnology (Shanghai) co., LTD 021-50676523 18019098996 info@acelybio.com China 3960 58
DC Chemicals 021-58447131 13564518121 sales@dcchemicals.com China 9409 58

View Lastest Price from Azacosterol dihydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Azacosterol hydrochloride pictures 2024-10-24 Azacosterol hydrochloride
1249-84-9
US $1520.00-1980.00 / mg 10g TargetMol Chemicals Inc.
Azacosterol dihydrochloride pictures 2024-08-11 Azacosterol dihydrochloride
1249-84-9
US $0.00-0.00 / KG 1KG 99.0% 10000KG Shaanxi Dideu Medichem Co. Ltd

1249-84-9(Azacosterol dihydrochloride)Related Search:

Azacosterol Azocosterol 2HCl Azocosterol Androst-5-en-3-ol, 17-[[3-(dimethylamino)propyl]methylamino]-, hydrochloride (1:2), (3β,17β)- Azacosterol dihydrochloride 1249-84-9 C25H44N2O2HCl C25H44N2O2ClH