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6132-10-1

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6132-10-1 Usage

Natural anabolic steroid

16-ketotestosterone is a naturally occurring anabolic steroid that is derived from testosterone.

Produced in the testes

It is produced in the testes and plays a crucial role in the development and maintenance of male reproductive tissues and secondary sexual characteristics.

Precursor to estrogen

It acts as a precursor to estrogen, which is essential for female development.

Role in protein synthesis and muscle growth

16-ketotestosterone plays a key role in the regulation of protein synthesis and muscle growth.

Anti-inflammatory and immunosuppressive properties

It is known to have anti-inflammatory and immunosuppressive properties.

Diverse physiological functions

16-ketotestosterone is an important hormone with diverse physiological functions in both males and females.

Check Digit Verification of cas no

The CAS Registry Mumber 6132-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6132-10:
(6*6)+(5*1)+(4*3)+(3*2)+(2*1)+(1*0)=61
61 % 10 = 1
So 6132-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O3/c1-18-7-5-12(20)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(21)17(19)22/h9,13-15,17,22H,3-8,10H2,1-2H3/t13-,14+,15+,17+,18+,19+/m1/s1

6132-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-morpholin-4-ylethyl)-2-(4-propan-2-ylphenyl)quinoline-4-carboxamide

1.2 Other means of identification

Product number -
Other names 16-Keto-testosterone

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:6132-10-1 SDS

6132-10-1Relevant articles and documents

Microbial transformation of androstenedione by Cladosporium sphaerospermum and Ulocladium chartarum

Yildirim, Kudret,Kuru, Ali,Kü?ükba?ol, Eda

, p. 7 - 14 (2019/05/15)

In this work, incubations of androstenedione 1 with Cladosporium sphaerospermum MRC 70266 and Ulocladium chartarum MRC 72584 have been reported. C. sphaerospermum MRC 70266 mainly hydroxylated 1 at C-6β, accompanied by a hydroxylation at C-15α, a reduction at C-17, a 5α-reduction and oxidations at C-6 and C-16 following hydroxylations. U. chartarum MRC 72584 hydroxylated 1 at C-6β, C-7α, C-7β and C-14α, accompanied by an oxidation at C-6 following its hydroxylation, a reduction at C-17 and a 5α-reduction. 6β,17β-Dihydroxyandrost-4-en-3,16-dione 8, one of the metabolites from the incubation of 1 with C. sphaerospermum MRC 70266, was determined as a new compound.

Microbial hydroxylation of steroids. Part 12. Hydroxylation of testosterone and related steroids by Gnomonia fructicola ATCC 11430

Holland,Brown,Chenchaiah,Chernishenko,Khan,Rao

, p. 268 - 274 (2007/10/02)

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