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(10α)-17β-Hydroxyandrost-4-en-3-one, commonly known as androstanolone or dehydroepiandrosterone (DHEA), is a hormone precursor and steroid that is naturally produced in the human body. It plays a vital role in the synthesis of other hormones, including testosterone and estrogen, and is also available as a supplement for various purposes.

604-39-7

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604-39-7 Usage

Uses

Used in Athletic Performance Enhancement:
(10α)-17β-Hydroxyandrost-4-en-3-one is used as a supplement for enhancing athletic performance. It is believed to increase muscle mass and strength, as well as improve physical capabilities.
Used in Mood Improvement:
(10α)-17β-Hydroxyandrost-4-en-3-one is used as a mood enhancer, as it has been shown to have positive effects on mood and well-being.
Used in Anti-Aging:
(10α)-17β-Hydroxyandrost-4-en-3-one is used as an anti-aging supplement, as it may help combat the effects of aging by maintaining hormone levels and promoting overall health.
Used in Medical Treatments:
(10α)-17β-Hydroxyandrost-4-en-3-one is used as a potential treatment for various medical conditions, such as depression, osteoporosis, and autoimmune disorders. However, it is important to approach the use of DHEA supplements with caution, as excessive intake can have adverse effects on the body.
Used in Pharmaceutical Industry:
(10α)-17β-Hydroxyandrost-4-en-3-one is used in the pharmaceutical industry for the synthesis of other hormones and as a starting material for the production of various medications.
Used in Research:
(10α)-17β-Hydroxyandrost-4-en-3-one is used in research settings to study the effects of hormones on the body and to develop new treatments for various conditions.

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 academic research and scientific papers

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.

A GENERAL METHOD FOR THE SELECTIVE REDUCTION OF KETONES IN THE PRESENCE OF ENONES.

Ward, Dale E.,Rhee, Chung K.,Zoghaib, Wajdi M.

, p. 517 - 520 (2007/10/02)

Ketones can be reduced in the presence of conjugated enones by sodium borohydride in 50percent methanol in dichloromethane at -78 deg C.The selectivity is generally excellent.In favorable cases the reaction can be carried out at room temperature in dichloromethane with acetic acid as catalyst.

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