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Step one: The first step in the synthesis of fluoxymesterone is the microbiological oxidation of commercially available androstenedione 1. Pyrrolidine then reacts to form an enamine 1. In subsequent steps, alkylation of the keto group 1. This involves more standard synthetic transformations. The resulting structure 1. Detection of halotestin and other such illegal anabolic steroids in sports is achieved by GS-MS identification of urinary excreted anabolic steroids and their metabolites. Sustanon 250 and many of its metabolites contain two polar hydroxyl groups, leading to intermolecular hydrogen bonding that increases their boiling point and reduces volatility. Fluoxymesterone was first described in Testosterone Mix was introduced for medical use in the United States in Availability of fluoxymesterone aside from the United States remains scarce, but it is marketed in some other countries such as MexicoMoldovaand Taiwan. From Wikipedia, the free encyclopedia. IUPAC name. Interactive image. Molecular Nutrition Llc. Lemke; David A. Williams 24 January Steroid Biochem.

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