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4731-15-1

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4731-15-1 Usage

Synthetic steroid

A synthetically produced steroid, which is a type of organic compound that resembles the chemical structure of naturally occurring steroids.

Derivative of androstenedione

It is derived from androstenedione, a naturally occurring steroid hormone.

Prohormone

It acts as a prohormone, meaning it can be converted into a more potent hormone in the body.

Bodybuilding supplement

It is commonly used as a supplement in the bodybuilding community to enhance muscle growth and performance.

Performance-enhancing drug

It is also used as a performance-enhancing drug in sports, due to its ability to increase muscle mass, strength, and endurance.

Anti-inflammatory effects

It has potential anti-inflammatory properties, which can help reduce inflammation in the body.

Anti-catabolic effects

It may have anti-catabolic effects, meaning it can help prevent the breakdown of muscle tissue.

Controversial use

Its use is controversial due to its potential for abuse and adverse health effects.

Banned in sports

Many sports organizations have banned its use due to its potential for abuse and health risks.

Chemical structure

The chemical structure of 11,17-dioxoandrostan-3-yl acetate consists of a steroid backbone with an acetate group attached to the 3-position and two ketone groups at the 11 and 17 positions.

Health risks

The use of 11,17-dioxoandrostan-3-yl acetate can lead to adverse health effects, including liver damage, cardiovascular issues, and hormonal imbalances.

Legal status

The legal status of 11,17-dioxoandrostan-3-yl acetate varies by country, with some countries classifying it as a controlled substance.

Detection in drug testing

It can be detected in drug testing, as it is a banned substance in many sports organizations.

Half-life

The half-life of 11,17-dioxoandrostan-3-yl acetate is relatively short, which means it is metabolized and eliminated from the body quickly.

Conversion to active hormones

In the body, 11,17-dioxoandrostan-3-yl acetate can be converted into more potent hormones, such as testosterone and dihydrotestosterone (DHT), which contribute to its anabolic and androgenic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 4731-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,3 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4731-15:
(6*4)+(5*7)+(4*3)+(3*1)+(2*1)+(1*5)=81
81 % 10 = 1
So 4731-15-1 is a valid CAS Registry Number.

4731-15-1SDS

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 [(8S,9S,10S,13S,14S)-10,13-dimethyl-11,17-dioxo-2,3,4,5,6,7,8,9,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names 6,7-Dihydro-6-(2-hydroxyethyl)-5H-dibenz(c,e)azepine

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:4731-15-1 SDS

4731-15-1Relevant articles and documents

Factors governing the relative stabilities of the C/D cis and trans ring junctures in delta8-11-keto steroids.

Patterson,Djerassi,Yuh,Allinger

, p. 2365 - 2370,2366, 2368 (2007/10/11)

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