Oral Primobolan-All About Methenolone Acetate

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Oral Primobolan or Methenolone acetate is an anabolic androgenic steroid that is famous worldwide for its unique muscle building properties. A favorite among European competitors, oral Primobolan is best used during cutting phases of training.

The active life of oral Primobolan is 4-6 hours and this steroid has the chemical name of 17ß-hydroxy-1-methyl-5a-androst-1-en-3-one acetate and its anabolic/androgenic ratio is 88:44-57. Primobolan (oral) is not c17 alpha alkylated like most oral steroids, which makes it ideal for those looking for a performance enhancing drug that does not result in elevated liver values, liver toxicity or damage.

Secondly, Methenolone acetate does not aromatize that makes it an ideal option for athletes who are prone to estrogenic side effects such as oily skin and gynecomastia. An excellent drug before a bodybuilding contest, oral Primobolan is the best choice for beginners and female athletes. Virilization symptoms are extremely uncommon with use of this drug.

Considered to be a better choice than Masteron, oral Primobolan can reverse many of the negative effects of anemia and has the ability to halt muscle wasting. This drug also has the ability to improve body's immunity levels and is therefore recommended to HIV/AIDS patients. A big majority of athletes prefer using the oral version of Primobolan when it comes to gaining and maintaining lean tissue. It is also a good option for athletes on a calorie-reduced diet and keen to retain muscle. Moreover, this steroid has the potential of improving nitrogen retention that in turn promotes buildup of muscle.

OralPrimobolan is best used between steroid cycles during "off-time" to maintain body strength and muscle mass gains. This rare androgen-based steroid is medically recommended to reduce breast tumors and causes less inhibition than Testosterone or Deca Durabolin in the context of anabolic effects. This is attributed to the fact that Primobolan is characterized by lack of conversion to Dihydrotestosterone, low central nervous system activity, and lack of aromatization to estrogen.