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(2alpha,5alpha,17beta)-17-hydroxy-2-(hydroxymethyl)-17-methylandrostan-3-one, commonly known as Mesterolone, is a steroidal compound with a chemical formula of C21H34O3. It is a derivative of the male sex hormone testosterone and possesses potent androgenic and anabolic properties.
Used in Pharmaceutical Industry:
Mesterolone is used as a medication for treating low testosterone levels and male infertility. It functions by increasing the levels of testosterone in the body and stimulating the production of sperm, thereby addressing hormonal imbalances and fertility issues.
Used in Sports and Bodybuilding:
Mesterolone is used as a performance-enhancing drug in bodybuilding and athletics. It is favored for its ability to increase muscle mass and strength, providing athletes and bodybuilders with a competitive edge in their respective sports.
However, it is important to note that the use of Mesterolone as a performance-enhancing drug is often prohibited in professional sports due to its potential for abuse and health risks associated with steroid use.

20592-44-3

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20592-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20592-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,9 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20592-44:
(7*2)+(6*0)+(5*5)+(4*9)+(3*2)+(2*4)+(1*4)=93
93 % 10 = 3
So 20592-44-3 is a valid CAS Registry Number.

20592-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-2-(hydroxymethyl)-10,13,17-trimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names -

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:20592-44-3 SDS

20592-44-3Downstream Products

20592-44-3Relevant academic research and scientific papers

Identification of drostanolone and 17-methyldrostanolone metabolites produced by cryopreserved human hepatocytes

Gauthier, Julie,Goudreault, Danielle,Poirier, Donald,Ayotte, Christiane

, p. 306 - 314 (2009)

Methyldrostanolone (2α,17α-dimethyl-17β-hydroxy-5α-androstan-3-one) was synthesized from drostanolone (17β-hydroxy-2α-methyl-5α-androstan-3-one) and identified in commercial products. Cultures of cryopreserved human hepatocytes were used to study the biot

The hydrogenation of alpha-hydroxymethylene-ketone derivatives to alpha-hydroxymethyl-ketone derivatives with a cell-free system of Streptomyces cinereocrocatus.

Oda,Sato,Sato

, p. 502 - 505 (1989)

2',3'-Dihydro-5'-formylgriseofulvin (3), oxymetholone (5), and 3 beta-acetoxy-16-acetoxymethylene-5-androsten-17-one (9) were used as the substrates of a cell-free system from Streptomyces cinereocrocatus NRRL 3443. The results indicated that S. cinereocrocatus contains enzymatic activities which reduce the above three alpha-hydroxymethylene-ketones to the corresponding alpha-hydroxymethyl-ketones.

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