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61630-32-8

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61630-32-8 Usage

Description

4-ANDROSTEN-4-OL-3,17-DIONE ACETATE, also known as 4-Androstene-3,17-dione acetate, is a synthetic chemical compound that functions as a prohormone. It is a derivative of the naturally occurring hormone testosterone, which means that it can be converted by the body into an active hormone, specifically testosterone. This conversion is believed to promote protein synthesis and enhance muscle recovery, making it a popular choice among athletes and bodybuilders.
Used in Fitness and Bodybuilding Industry:
4-ANDROSTEN-4-OL-3,17-DIONE ACETATE is used as a supplement for increasing muscle mass, strength, and athletic performance. It is favored by athletes and bodybuilders looking to improve their physical performance and body composition due to its potential to boost protein synthesis and muscle recovery.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 4-ANDROSTEN-4-OL-3,17-DIONE ACETATE, being a testosterone derivative, could potentially be used in the pharmaceutical industry for hormone replacement therapy or other treatments that require modulation of testosterone levels. However, it is important to note that the use in this industry would be subject to regulatory approval and safety assessments.

Check Digit Verification of cas no

The CAS Registry Mumber 61630-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,3 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61630-32:
(7*6)+(6*1)+(5*6)+(4*3)+(3*0)+(2*3)+(1*2)=98
98 % 10 = 8
So 61630-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H28O4/c1-12(22)25-19-16-5-4-13-14-6-7-18(24)21(14,3)10-8-15(13)20(16,2)11-9-17(19)23/h13-15H,4-11H2,1-3H3/t13-,14-,15-,20+,21-/m0/s1

61630-32-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Androsten-4-ol-3,17-dione acetate

1.2 Other means of identification

Product number -
Other names [(8R,9S,10R,13S,14S)-10,13-dimethyl-3,17-dioxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61630-32-8 SDS

61630-32-8Downstream Products

61630-32-8Relevant articles and documents

3,17-Dioxoandrost-4-en-4-yl acetate

Andrade,Paixao,De Almeida,Fernandes Roleira,Tavares Da Silva

, p. o330-o331 (2007)

The title compound, C21H28O4, has a 4-acet-oxy substituent positioned on the steroid face. The six-membered ring A assumes a conformation inter-mediate between 1,2Β-half chair and 1-sofa. A long Csp 3 - Csp 3 bond is observed in ring B and reproduced in quantum-mechanical ab initio calculations of the isolated mol-ecule using a mol-ecular-orbital Hartree-Fock method. Cohesion of the crystal can be attributed to van der Waals inter-actions and weak C - H...O hydrogen bonds. International Union of Crystallography 2007.

Topical treatment for mastalgia

-

, (2008/06/13)

A composition for medicinal treatment by means of topical administration is described, which contains an aromatase inhibitor, in addition to conventional constituents of topical forms of administration. The active ingredient or the composition containing this active ingredient is especially suitable for the prophylaxis and for the treatment of mastalgia.

The Synthesis of 4-Hydroxyandrost-4-ene-3,17-dione and other Potential Aromatase Inhibitors

Mann, John,Pietrzak, Barbara

, p. 2681 - 2685 (2007/10/02)

We describe novel syntheses of 4-hydroxyandrost-4-ene-3,17-dione (Ia) and related compounds, some containing fluorine.In addition we provide further evidence of the general tendency of 2- and 6-substituted androst-4-ene-3,17-diones to undergo rearrangement reactions, and thus provide new routes to 6-fluoro- and 2,6-difluoro-derivatives.Several of these compounds are potent aromatase inhibitors.

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