METHYLDIAZIRINOL

Methyldiazirinol was first synthesized by researchers at Lederle Laboratories, a subsidiary of American Cyanamid. Their results were reported in 1965. They patented the invention in 1966. Lederle/American Cyanamid also synthesized some 2a-cyano-substituted compounds similar to Cynostane.Methyldiazirinol was one of many steroids listed in Julius Vida's Androgens and Anabolic Agents. In a section detailing “Compounds displaying decreased androgenic activity coupled with increased anabolic activity”, the 3,3-azo steroid is listed alongside steroids such as oxandrolone (anavar), methenolone (primobolan), stanozolol (winstrol) and norbolethone (one version of “the Clear”).According to the Lederle Laboratories researchers, the Methyldiazirinol has an oral anabolic:androgenic ratio of 300:20 when compared to methyl testosterone, giving it a "Q factor" of 15. This provides anabolic to androgenic effects similar to the recently-banned methasterone (superdrol), which was reported to have an anabolic:androgenic ratio of 400:20.

HEXADRONE

6a-Chloro-androst-4-en-17b-ol-3-one represents the next generation of legal androgens: Extremely effective, dry, and non-methylated, it stacks well with everything, and is more than adequate for solo runs.Powerful anabolic, rated at 300:1 (anabolic:androgenic) vs. testosterone. Cannot convert to estrogen; immune to the effects of aromatase.Intrinsically active compound with no conversion required.Non-methylated, yet resistant to some aspects of CYP-mediated metabolism due to the Chloro group at C6.In terms of results, this 6-chlorinated compound is equal to harsher androgens such as M1, 4ADD and Halodrol. In terms of toxicity, this compound cannot even be compared to them. It's much safer and much milder.

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