28816-02-6

Basic information

• Product Name: 17a-17B-Hydroxyandrosta-1,4,6-trien-3-one
• Synonyms: 17a-17B-Hydroxyandrosta-1,4,6-trien-3-one;17α-METHYL-1,4,6-ANDROSTARIENE-17β-OL-3-ONE;17A-METHYL-17SS-HYDROXY-ANDROSTA-1,4,6-TRIEN-3-ONE
• CAS NO: 28816-02-6
• Molecular Formula: C19H24O2
• Molecular Weight: 284.39266
• Mol File: 28816-02-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 453.1°Cat760mmHg
• Flash Point: 193°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 4.08E-10mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: 17a-17B-Hydroxyandrosta-1,4,6-trien-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 17a-17B-Hydroxyandrosta-1,4,6-trien-3-one(28816-02-6)
• EPA Substance Registry System: 17a-17B-Hydroxyandrosta-1,4,6-trien-3-one(28816-02-6)

Safety Data

• Hazardous Substances Data: 28816-02-6(Hazardous Substances Data)

Usage

Type of compound

Synthetic androstane steroid

Derivative of

Dihydrotestosterone (DHT)

Potency

Potent androgenic and anabolic steroid

Usage

Performance-enhancing drug

Effects

Strong anabolic effect, relatively weak androgenic properties

Popularity

Among athletes and bodybuilders seeking to increase muscle mass and strength

Competitive sports

Use is banned

Side effects

Liver toxicity, cardiovascular issues

Health risks

Restricted production and distribution in many countries

InChI:InChI=1/C20H26O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h4-6,9,12,15-17,22H,7-8,10-11H2,1-3H3/t15-,16+,17+,18+,19+,20?/m1/s1

Upstream product

• 72-63-9 metandienone 

Relevant articles and documents

Imitation of phase i oxidative metabolism of anabolic steroids by titanium dioxide photocatalysis

The aim of this study was to investigate the feasibility of titanium dioxide (TiO2) photocatalysis for oxidation of anabolic steroids and for imitation of their phase I metabolism. The photocatalytic reaction products of five anabolic steroids were compared to their phase I in vitro metabolites produced by human liver microsomes (HLM). The same main reaction types - hydroxylation, dehydrogenation and combination of these two - were observed both in TiO2 photocatalysis and in microsomal incubations. Several isomers of each product type were formed in both systems. Based on the same mass, retention time and similarity of the product ion spectra, many of the products observed in HLM reactions were also formed in TiO2 photocatalytic reactions. However, products characteristic to only either one of the systems were also formed. In conclusion, TiO2 photocatalysis is a rapid, simple and inexpensive method for imitation of phase I metabolism of anabolic steroids and production of metabolite standards.