99% Anabolic Steroid Powder Halotestin Fluoxymesterone for Bodybuilding

99% Anabolic Steroid Powder Halotestin Fluoxymesterone for Bodybuilding CAS 76-43-7

Synonyms:11-beta,17-beta-Dihydroxy-9-alpha-fluoro-17-alpha-methyl-4-androster-3-one;17-alpha-methyl-9-alpha-fluoro-11-beta-hydroxytesterone;17-alpha-Methyl-9-alpha-fluoro-11-beta-hydroxytestosterone;9-alpha-fluoro-11-beta,17-beta-dihydroxy-17-alpha-methyl-4-androstene-3-one;9alpha-Fluoro-11beta,17beta-dihydroxy-17alpha-methyl-4-androstene-3-one;9-alpha-fluoro-11-beta-hydroxy-17-methyltestosterone;9alpha-Fluoro-11beta-hydroxy-17-methyltestosterone;9-alpha-Fluoro-17-alpha-methyl-11-beta,17-dihydroxy-4-androsten-3-one

CAS:76-43-7

MF:C20H29FO3

MW:336.44

EINECS:200-961-8

Product Categories:Organics;chiral;Steroids;Steroid and Hormone;Intermediates & Fine Chemicals;Pharmaceuticals;API;teroids;Inhibitors

Mol File:76-43-7.mol

Chemical Properties:white to light yellow crystal powde

Description

Fluoxymesteron is an extremely powerful anabolic androgenic steroid that was first released in the late 1950's by Upjohn under the trade name Halotestin. Shortly after, Ciba Pharmaceuticals would release the hormone under the Ultandren name, but Halotestin has remained the most recognizable brand name. Pharmacia, formerly Upjohn, now manufactures the Halotestin brand name.

Fluoxymesteron (Halotestin) Usage

Fluoxymesteron Halotestin is an anabolic steroide with strong androgenic properties that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women. It is approximately 5 times as potent as methyltestosteron. The antitumor activity of fluoxymesteron appears related to reduction or competitive inhibition of prolactin receptors or estrogen receptors or production.

Fluoxymesteron  Halotestin Function & Traits

Fluoxymesteron is a testosteron derived anabolic androgenic steroid or more specifically a structurally altered form of Methyltestosteron. Halotestin is the testosteron hormone with an added methyl group at the 17th carbon position to allow oral ingestion. It also possesses an added fluoro group at carbon 9 and 3 and a hydroxyl group at carbon 11. These modifications inhibit the steroid's aromatization and greatly increase its androgenic nature. The androgenic nature and activity of Halotestin will be far beyond Methyltestosterone.