Methenolone is one of the unique compounds that can be administered either orally or by injection. The only difference in the compounds is the ester attached, the oral version using acetate and the injectable version using enanthate. However regardless of the method of administration or ester used methenolone is considered by most to be a relatively mild compound. For the most part users should not expect to make major gains in muscle mass from this drug but rather lean gains in muscular body weight. In some animal studies (1,2) it has been demonstrated that methenolone has the potential to increase muscular size and strength. However the anecdotal evidence from users suggest that any mass gains using the compound will not be overly significant. However it has been noted as quite an effective “cutting” drug because of it’s ability to bind to the androgen receptors in the body (3). Of course the ability to bind to androgen receptors has been shown to promote fat burning in individuals. This effect would obviously be highly desirable during “cutting” phases or to simply limit the amount of body fat one puts on during a bulking phase. Methenolone does not convert to estrogen and therefore estrogenic side effects should not be a concern with this compound. As well, unlike other oral anabolic steroids it is not 17 alpha alkylated. This means that it is far less stressful to the liver than other oral steroids. However the process that oral methenolone does go through to make it orally active, 1 alkylation and 17-beta esterification, does not protect it during the first pass through the liver very well at all. This requires that the oral version of methenolone must be run at higher doses than would be expected with the injectable version. For this reason it is often said that the injectable version of the drug is far more efficient at producing gains.
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