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3381-88-2

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3381-88-2 Usage

Defination

Methasterone, also known as methyldrostanolone and known by the nickname Superdrol, is a synthetic and orally active anabolic–androgenic steroid (AAS) which was never marketed for medical use. It was brought to the black market, instead, in a clandestine fashion as a "designer steroid."

Designer steroid

It was in late 2005 that the reclassification of methasterone as AAS (as well as that of four other designer steroids) was brought to public awareness via an article published in the Washington Post. Don Catlin of the UCLA Olympic Laboratory, who conducted the studies, noted methasterone's similarity to drostanolone. A warning by the FDA was issued soon after to the general public as well as to the distributor, Designer Supplements LLC, for the marketing of this compound.?Methasterone was subsequently added to the World Anti-Doping Agency (WADA) list of prohibited substances in sport. Despite all of this, methasterone has resurfaced within the supplement industry on several occasions since its banning by WADA.

Uses

Methasterone is an anabolic androgenic steroid. Methasterone is one of the anabolic steroids screened by the World Anti-Doping Agency (WADA).

Synthesis

Methasterone is synthesized by Catalytic Oxymetholone in ethanol with the presence palladium on charcoal. Procedure: 2.05 g Oxymetholone was dissolved in 160 ml ethanol at room temperature. This solution was hydrogenated in a pressure vessel (Parr reactor) with 2.50 g palladium on charcoal (5%) at 3 bar and room temperature for 36 h. The reaction seemed to be completed, since there is no 5 starting material remaining. The formation of two major byproducts can be observed via TLC (Seebach-staining). The mixture was filtered through a short pad of silica and the corresponding ethanol solution was evaporated to yield 1.90 g of a colorless solid. The crude product was purified by column chromatography on silica gel by using hexane-ethyl acetate (1:1), to afford 1.35 g of Methasterone as a colorless solid (68%).

Check Digit Verification of cas no

The CAS Registry Mumber 3381-88-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3381-88:
(6*3)+(5*3)+(4*8)+(3*1)+(2*8)+(1*8)=92
92 % 10 = 2
So 3381-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O2/c1-13-12-19(2)14(11-18(13)22)5-6-15-16(19)7-9-20(3)17(15)8-10-21(20,4)23/h13-17,23H,5-12H2,1-4H3/t13-,14+,15-,16+,17+,19+,20+,21+/m1/s1

3381-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-2,10,13,17-tetramethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names 2alpha,17alpha-Dimethyldihydrotestosterone

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:3381-88-2 SDS

3381-88-2Upstream product

3381-88-2Downstream Products

3381-88-2Relevant articles and documents

STEROIDS. CCIX. RING A MODIFIED HORMONE ANALOGS. V.

EDWARDS,CALZADA,BOWERS

, p. 178 - 182 (2007/10/10)

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