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5α-Androstan-16-one, also known as 5α-androst-16-en-3-one, is a synthetic anabolic steroid derived from the naturally occurring hormone dihydrotestosterone (DHT). It is a potent androgen, which means it has strong masculinizing effects on the body. This chemical is not approved for human consumption and is not legally available for sale as a dietary supplement in many countries due to its potential health risks and side effects, which can include liver toxicity, hormonal imbalances, and cardiovascular issues. It is important to note that the use of such substances is typically regulated and can have serious consequences for health and legal compliance.

1032-16-2

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1032-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1032-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1032-16:
(6*1)+(5*0)+(4*3)+(3*2)+(2*1)+(1*6)=32
32 % 10 = 2
So 1032-16-2 is a valid CAS Registry Number.

1032-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 15α-androstane-16-one

1.2 Other means of identification

Product number -
Other names 16-androstanone

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:1032-16-2 SDS

1032-16-2Relevant academic research and scientific papers

Mechanistic studies of deoxygenation of steroidal ring-D 16,17-ketols with trimethylsilyl iodide

Nagaoka, Masao,Nagasawa, Etsuko,Sato, Sadao,Numazawa, Mitsuteru

, p. 548 - 553 (2007/10/03)

Deoxygenation reaction of steroidal 16,17-ketols 1, 2 and 6 as well as their silyl ethers 3 and 7 and 16- and 17-iodoketone analogs 11, 12, and 14 with trimethylsilyl iodide (TMSI) or HI under various conditions was examined. The results indicate that the deoxygenation producing 16- and 17- ketones 9 and 8 proceeds through multiple reaction pathways; a direct iodination of a siloxy group of the ketol silyl ethers by iodide ion to give the iodoketones (path b), addition of TMSI to a carbonyl group of the ketol silyl ethers to yield diiodo derivatives 22 and 23 through iodo-bis-TMS compounds 20 and 21 (path a), and cleavage of ether bond of dimers 15-18 initially produced are, at least, involved. In these sequences, rearrangement of the 16-ketols 1 and 2 to the 17 β-ketol 6 also plays a significant role. The yields of the ketones 9 and 8 and their relative amounts would be dependent on the relative importance of each pathway in the reaction.

Deoxygenation of steroidal ring-D 16,17-ketols with trimethylsilyl iodide

Nagaoka, Masao,Nagasawa, Etsuko,Numazawa, Mitsuteru

, p. 1857 - 1861 (2007/10/03)

Reaction of various steroidal 16,17-ketols, 16α-hydroxy-17-ketones 1- 3, and 15, 16β-hydroxy-17-ketone 4, and 17β-hydroxy-16-ketones 5-7, and 17, along with methyl ethers of 16α- and 17β-ketols 1 and 5, with an excess of trimethylsilyl iodide (TMSI) or with HI in CHCl3, produced the deoxygenated products, a mixture of the corresponding 17- and 16-ketones, in low to quantitative yields, in which the 17-ketone was the major product in each ease. When the 16β-deuterated 16α-ketol 3 and the 17α-deuterated 17β- ketol 7 were reacted with TMSI for a brief period (15 min), the deuterium content at C-16β and C-17α of the recovered steroids 3 and 7 was reduced by 17 and 35%, respectively. The present results indicate that the deoxygenation proceeds not only through a direct iodination pathway producing α-iodoketone but also through other reaction pathways.

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