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29907-31-1

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29907-31-1 Usage

Chemical compound

A derivative of the male sex hormone, testosterone.

Classification

An androstane steroid.

Metabolite

A major metabolite of the potent androgenic steroid 11-ketotestosterone.

Potential use

Studied for its potential as a performance-enhancing drug.

Role

Investigated for its role in the regulation of male sexual characteristics and behavior.

Therapeutic potential

Explored for its possible use in treating androgen insensitivity syndrome and certain forms of male infertility.

Research status

The use and effects of this compound in humans are still being researched.

Medical approval

Not approved for medical use in most countries.

Check Digit Verification of cas no

The CAS Registry Mumber 29907-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,0 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29907-31:
(7*2)+(6*9)+(5*9)+(4*0)+(3*7)+(2*3)+(1*1)=141
141 % 10 = 1
So 29907-31-1 is a valid CAS Registry Number.

29907-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 11α-hydroxy-5α-androstane-3,17-dione

1.2 Other means of identification

Product number -
Other names 11α-hydroxy-5α-androstan-3,17-dione

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:29907-31-1 SDS

29907-31-1Upstream product

29907-31-1Relevant articles and documents

The hydroxylation of some 13α-methylsteroids by Cephalosporium aphidicola

Boynton, Juliette,Hanson, James R.,Hunter, A. Christy

, p. 951 - 956 (2007/10/03)

The Fungus, Cephalosporium aphidicola, has been shown to hydroxylate 5α,13α-androstan-3,17-dione and the 3β-alcohol at the C-1α and C-7α positions, whereas the corresponding compounds in the normal 13β-methyl series are hydroxylated at the C-11α and C-14α positions. Both series were hydroxylated at the 5α position. There was some epimerization of the axial 3α-alcohols to the equatorial 3β-epimers.

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