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604-39-7

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604-39-7 Usage

General Description

(10α)-17β-Hydroxyandrost-4-en-3-one, also known as "androstenolone" or "dehydroepiandrosterone (DHEA)," is a hormone precursor and steroid that is naturally produced in the body. It plays a crucial role in the synthesis of other hormones such as testosterone and estrogen. DHEA is also available as a supplement and is used for various purposes such as enhancing athletic performance, improving mood, and combating the effects of aging. Additionally, it has been studied for its potential benefits in treating conditions such as depression, osteoporosis, and autoimmune disorders. However, the use of DHEA supplements should be approached with caution, as excessive intake can have adverse effects on the body.

Check Digit Verification of cas no

The CAS Registry Mumber 604-39-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 604-39:
(5*6)+(4*0)+(3*4)+(2*3)+(1*9)=57
57 % 10 = 7
So 604-39-7 is a valid CAS Registry Number.

604-39-7SDS

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 17β-hydroxy-(10α)-androst-4-en-3-one

1.2 Other means of identification

Product number -
Other names 17β-Hydroxy-Δ4-9β.10α-androsten-3-on

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:604-39-7 SDS

604-39-7Relevant articles and documents

Biotransformation of androst-4-ene-3,17-dione by some fungi

Yildirim, Kudret,Kuru, Ali,Keskin, Ece,Salihoglu, Aylin,Bukum, Neslihan

, p. 594 - 597 (2017/11/14)

The incubations of androst-4-ene-3,17-dione with Aspergillus candidus MRC 200634, Aspergillus tamarii MRC 72400, Aspergillus wentii MRC 200316 and Mucor hiemalis MRC 70325 for 5 days are reported. A. candidus MRC 200634 mainly hydroxylated androst-4-ene-3,17-dione at C-11α, C-15α and C-15β whilst A. wentii MRC 200316 hydroxylated it mainly at C-6β. A. tamarii MRC 72400 showed predominately a Baeyer–Villiger monooxygenase activity. M. hiemalis MRC 70325 hydroxylated the substrate at C-14α and reduced most of it at C-17.

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