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Bolasterone

CAS No.
1605-89-6
Chemical Name:
Bolasterone
Synonyms
Myagen;7α,17α-DiMethyltes;7,17-Dimethyltestosterone;Bolasterone (1.0mg/ml in Acetonitrile);4-ANDROSTEN-7α, 17α-DIMETHYL-17β-OL-3-ONE;17-Hydroxy-7,17-dimethyl-4-androsten-3-one;17β-Hydroxy-7α,17-diMethyl- androst-4-en-3-one;17β-Hydroxy-7α,17α- diMethylandrost-4-ene-3-one;(7α,17β)-17-Hydroxy-7,17-diMethylandrost-4-en-3-one;Androst-4-en-3-one, 17-hydroxy-7,17-dimethyl-, (7α,17β)-
CBNumber:
CB3875054
Molecular Formula:
C21H32O2
Molecular Weight:
316.48
MDL Number:
MOL File:
1605-89-6.mol
Last updated:2023-05-15 10:43:59

Bolasterone Properties

Melting point 163-165°
Boiling point 441.0±45.0 °C(Predicted)
Density 1.09±0.1 g/cm3(Predicted)
solubility Chloroform (Slightly), Dioxane (Slightly), Methanol (Slightly)
form Solid
pka 15.13±0.70(Predicted)
color Off-White to Pale Yellow
FDA UNII T7ZM08F7FU

SAFETY

Risk and Safety Statements

DEA Controlled Substances CSCN: 4000
CSA SCH: Schedule III
NARC: No

Bolasterone price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation SHG0004762 BOLASTERONE 95.00% 1605-89-6 10MG $750.75 2021-12-16 Buy
American Custom Chemicals Corporation SHG0004762 BOLASTERONE 95.00% 1605-89-6 100MG $1963.5 2021-12-16 Buy
Product number Packaging Price Buy
SHG0004762 10MG $750.75 Buy
SHG0004762 100MG $1963.5 Buy

Bolasterone Chemical Properties,Uses,Production

Originator

Myagen,Upjohn

Uses

Synthetic anabolic; epimeric with Calusterone (C148900). Controlled substance (anabolic steroid).

Definition

ChEBI: Bolasterone is a 3-hydroxy steroid. It has a role as an androgen.

Manufacturing Process

A mixture of 0.4 g of cuprous chloride, 20 ml of 4 M methylmagnesium bromide in ether and 60 ml of redistilled tetrahydrofuran was stirred and cooled in an ice bath during the addition of a mixture of 2.0 g of 6-dehydro- 17-methyltestosterone, 60 ml of redistilled tetrahydrofuran and 0.2 g of cuprous chloride. The ice bath was removed and stirring was continued for 4 h. Ice and water were than carefully added, the solution acidified with 3 N hydrochloric acid and extracted several times with ether. The combined ether extracts were washed with a brine-sodium carbonate solution, brine and then g column of magnesium silicate (Florisil) packed wet with hexanes (Skellysolve B). The column was eluted with 250 ml of hexanes, 0.5 liter of 2% acetone, two liters of 4% acetone and 3.5 L of 6% acetone in hexanes.
The residues from fractions 8 to 16 were combined and rechromatographed over a 125.0 g column of magnesium silicate. The column was eluted with 6% acetone in hexanes. Fractions 18 to 29 were combined and dissolved in acetone, decolorized with charcoal, and recrystallized from acetone. 1.0 g of a crystalline mixture of the 7-epimers of 7,17-dimethyltestosterone was obtained melting at 120° to 140°C. The 7α-isomer are separated according to following procedure:
To obtain the 7(α)-isomer of 7,17-dimethyltestosterone the crystalline mixture of the 7 stereoisomers of 7,17-dimethyltestosterone was refluxed in tertiary butyl alcohol with recrystallized chloranil under nitrogen. The reaction mixture was concentrated under a fast stream of nitrogen, diluted with methylene chloride and the solution washed with dilute sodium hydroxide, water and then dried, filtered and the solvent removed. The residue, was combined with the product from an identical run and chromatographed through a magnesium silicate column developed with solvent of the following composition and order:
two each of hexane hydrocarbons (Skellysolve B), hexanes plus 4% acetone, hexanes plus 8% acetone, hexanes plus 12% acetone, hexanes plus 14% acetone, hexanes plus 16% acetone, hexanes plus 18% acetone, hexanes plus 20% acetone, hexanes plus 24% acetone, hexanes plus 28% acetone, and two of acetone.
The residues, eluted with mixture: water-acetone, were combined and chromatographed through a 50 g 1:1 charcoal (Darco)-diatomaceous earth (Celite) column. The column was developed with solvent of the following composition and order: methanol, a 1:1 mixture of methanol and acetone, a 1:2 mixture of methanol and acetone, acetone and a 1:4 mixture of acetone and methylene chloride. Fractions, containing 7(α)-epimer were combined, the solvent evaporated and the residue crystallized from acetone to give the 7α,17-dimethyltestosterone, melting point at 163° to 165°C.

Therapeutic Function

Anabolic

Bolasterone Preparation Products And Raw materials

Bolasterone Suppliers

Global( 13)Suppliers
Supplier Tel Email Country ProdList Advantage
Wuhan senwayer century chemical Co.,Ltd
+undefined-27-86652399 +undefined13627115097 market02@senwayer.com China 881 58
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15421 60
Shanghai Ruipu Medical Technology Co., Ltd 15895968936 1018762393@qq.com China 9917 58
Pushan Industry (Shaanxi) Co., Ltd. 029-81310890 13571859809 info@pushanshiye.com China 10004 58
Shanghai Saikerui Biotechnology Co. , Ltd. 021-58000709 15900491054 info@scrbio.com China 9260 58

View Lastest Price from Bolasterone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bolasterone pictures 2023-11-27 Bolasterone
1605-89-6
US $8800.00 / kg 0.1kg 99% 20 tons Wuhan Senwayer Century Chemical Co.,Ltd
  • Bolasterone pictures
  • Bolasterone
    1605-89-6
  • US $8800.00 / kg
  • 99%
  • Wuhan Senwayer Century Chemical Co.,Ltd
7,17-Dimethyltestosterone Myagen (7α,17β)-17-Hydroxy-7,17-diMethylandrost-4-en-3-one 17β-Hydroxy-7α,17-diMethyl- androst-4-en-3-one 17β-Hydroxy-7α,17α- diMethylandrost-4-ene-3-one 7α,17α-DiMethyltes (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,10,13,17-tetramethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one 17-Hydroxy-7,17-dimethyl-4-androsten-3-one Bolasterone (1.0mg/ml in Acetonitrile) Androst-4-en-3-one, 17-hydroxy-7,17-dimethyl-, (7α,17β)- 4-ANDROSTEN-7α, 17α-DIMETHYL-17β-OL-3-ONE 1605-89-6 Intermediates & Fine Chemicals Pharmaceuticals Steroids