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29430-22-6

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29430-22-6 Usage

Type

Synthetic androgen and anabolic steroid

Origin

Derived from the hormone testosterone

Medical use

Treatment of low testosterone levels in men

Administration method

Injection

Release mechanism

Slowly released into the bloodstream over time

Effect

Provides a sustained hormonal effect

Performance-enhancing use

Increases muscle mass and strength

Legal status for non-medical purposes

Illegal

Health risks

Serious health consequences if used for non-medical purposes

Check Digit Verification of cas no

The CAS Registry Mumber 29430-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,3 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29430-22:
(7*2)+(6*9)+(5*4)+(4*3)+(3*0)+(2*2)+(1*2)=106
106 % 10 = 6
So 29430-22-6 is a valid CAS Registry Number.

29430-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name testosterone octanoate

1.2 Other means of identification

Product number -
Other names 17beta-Hydroxyandrost-4-en-3-one octanoate

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:29430-22-6 SDS

29430-22-6Downstream Products

29430-22-6Relevant articles and documents

Boosting the Catalytic Performance of Metal–Organic Frameworks for Steroid Transformations by Confinement within a Mesoporous Scaffold

Cirujano, Francisco G.,Luz, Ignacio,Soukri, Mustapha,Van Goethem, Cedric,Vankelecom, Ivo F. J.,Lail, Marty,De Vos, Dirk E.

supporting information, p. 13302 - 13306 (2017/10/17)

Solid-state crystallization achieves selective confinement of metal–organic framework (MOF) nanocrystals within mesoporous materials, thereby rendering active sites more accessible compared to the bulk-MOF and enhancing the chemical and mechanical stability of MOF nanocrystals. (Zr)UiO-66(NH2)/SiO2 hybrid materials were tested as efficient and reusable heterogeneous catalysts for the synthesis of steroid derivatives, outperforming the bulk (Zr)UiO-66(NH2) MOF. A clear correlation between the catalytic activity of the dispersed Zr sites present in the confined MOF, and the loading of the mesoporous SiO2, is demonstrated for steroid transformations.

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