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Stanozolol Injection is by far one of the most popular anabolic steroids of all time; in fact, it is one of the few steroids a non-steroid user might be able to name. This is an anabolic steroid that has gained worldwide media attention numerous times. It was the Stanozolol hormone that made headlines during the 1988 Olympics when Ben Johnson was stripped of his medal, and has been linked to the MLB more times than can be counted. Stanozolol is one of the oldest anabolic steroids we have in existence. While far from the oldest it does date back to the 1950’s. The Stanozolol hormone was first developed by Winthrop Laboratories under the trade name Winstrol. The Stanozolol hormone has since been found under numerous brand names across the globe, but the Winstrol name has remained the most popular and well recognized.

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Stanozolol is a dihydrotestosterone (DHT) based anabolic steroid. Specifically, Stanozolol is a structurally altered form of the DHT hormone, two specific changes to DHT that give us Stanozolol. The first modification is the addition of an attached pyrazol group at the A-ring in place of the 3-keto group. This makes Stanozolol a heterocyclic steroid. The second change is the addition of a methyl group. This change takes places at the 17th carbon position and puts Stanozolol into the 17-alpha alkylated (C17-aa) category. The structural changes made to DHT that give us Stanozolol reduce the hormone’s androgenicity dramatically and greatly increase its anabolic activity. Stanozolol carries an Anabolic Rating of 320 and an Androgenic Rating of 20 and real life use will match up to these structural ratings very well.

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One obvious difference between Winstrol Depot and other injectables is that it is not esterified, being sold as aqueous stanozolol suspension. (It should not be called water-soluble: virtually none of it is dissolved in the water.) This means that it does not have a classical half-life, where at time x the level is Ѕ the starting level, at time 2 x the level is ј, at time 3 x the level is 1/8, etc. Instead, the microcrystals slowly dissolve, and when they have all dissolved levels of the drug then fall very rapidly.

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