(5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate

Basic Information

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CAS Number

434-05-9

Molecular Formula

C22H32O3

Molecular Weight

344.5 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Ketones

Basic Chemical Raw Materials Organic Chemicals Esters

Basic Chemical Raw Materials Organic Chemicals Ethers

Fine Chemicals Surfactants Anionic Surfactants

Polymers and Plastics Thermoplastics Polyolefins

Basic Physical Properties

Physical State

Powder

Melting Point

138-139°

Boiling Point

419.57°C (rough estimate)

Refractive Index

1.5000 (estimate)

SMILES

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CC1=CC(=O)CC2C1(C3CCC4(C(C3CC2)CCC4OC(=O)C)C)C

InChI

InChI=1S/C22H32O3/c1-13-11-16(24)12-15-5-6-17-18-7-8-20(25-14(2)23)21(18,3)10-9-19(17)22(13,15)4/h11,15,17-20H,5-10,12H2,1-4H3/t15-,17-,18-,19-,20?,21-,22-/m0/s1

InChIKey

PGAUJQOPTMSERF-SFQBHUMCSA-N

LogP

4.696000000000004

Topological Polar Surface Area

43.370000000000005 Å²

Hydrogen Bond Donor/Acceptor

0 / 3

Complexity

635

Synonyms & References

English

SH-567
5-alpha-ANDROST-1-EN-3-ONE, 17-beta-HYDROXY-1-METHYL-, ACETATE
CHEMBL2106880
NSC74226
METHENOLONE 17-ACETATE [MI]
Methenolone (acetate)
SH 567
Methenolone acetate
Primonabol
UNII-W75590VPKQ
Primobolan (TN)
Androst-1-en-3-one, 17-(acetyloxy)-1-methyl-, (5.alpha.,17.beta.)-
SO 16496
NS00002106
A826271
Androst-1-en-3-one, 17-(acetyloxy)-1-methyl-, (5a,17b)-
METENOLONE ACETATE [JAN]
Metenolone acetate (JP17)
NCGC00484057-01
[(5S,8R,9S,10S,13S,14S,17S)-1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] acetate
metenolone acetate
Methenolone acetat
SH 567a
Testosterone,5.alpha.-dihydro-1-methyl-, acetate
W-106232
Primobolone
17beta-Hydroxy-1-methyl-5alpha-androst-1-en-3-one acetate
NSC-74226
NSC 74226
Premobolan
SQ-16496

MDL Number

MFCD00864181

Customs Code

2942000000

FAQ

What regulatory guidelines apply to (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9)?

The compound (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) is subject to various regulatory guidelines including the Globally Harmonized System of Classification and Labelling of Chemicals (GHS), Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) in the EU, and requirements set by the Food and Drug Administration (FDA) and Environmental Protection Agency (EPA) in the USA. It is important to comply with local and international regulations for its handling, storage, and disposal.

Are there alternatives to (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) in synthesis?

In synthesis, alternatives to (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) include similar steroidal acetates and other steroidal derivatives. Common alternative reagents and synthetic routes may involve using different precursors like androstenedione or other androstane derivatives, which can provide similar functional groups for analogous reactions.

What is the market or research trend for (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9)?

The market for (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) is primarily driven by its use in pharmaceutical and cosmetic industries. Recent research trends focus on its potential applications in hormone replacement therapy and as a precursor in steroid synthesis. The demand is expected to grow due to increasing interest in personalized medicine and cosmetic products with natural ingredients.

How should waste containing (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) be handled?

Waste containing (5alpha)-1-Methyl-3-oxoandrost-1-en-17-yl acetate (CAS: 434-05-9) should be handled according to local and international hazardous waste regulations. Collection and incineration by professional waste disposal services are recommended to ensure safe disposal. Proper environmental protection measures, such as preventing contamination of soil and water, should be implemented throughout the disposal process.