The truth is simple; there is no steroid like Trenbolone and while it may carry some potential adverse effects many men will supplement with no problem at all. You will find no steroid to pack such a punch on its own; in-fact, there are very few combinations and stacks that can be as potent as the Trenbolone hormone is on its own. For bulking and cutting this steroid has no equal and when combined with testosterone as it should be, if for no other reason than your health it is a hormone that cannot be beat safely making Trenbolonethe greatest anabolic androgenic steroid of all time.
Trenbolone is without a doubt one of the most beneficial anabolic steroids on the market. When we consider the therapeutic benefits of Nandrolone, or even Testosterone, it may not quite match up but on the basis of raw power and physique transformation Trenbolone Acetate is the king. No steroid will be as beneficial when cutting, not even close, and when bulking it is nothing short of fantastic. While Tren is beneficial during cutting and bulking phases, if you’re only going to use it in one phase always choose cutting. Many will actually need to limit their Trenbolone Acetate use to one phase due to the harshness of the compound in some men, especially when we consider cardiovascular strain. However, solid responders who are in excellent health should find they can use the steroid during both phases with a high level of success.
Trenbolone acetate is a modified form of nandrolone.  The structure of trenbolone acetate is a 19-nor classification, which represents a structural change of the testosterone hormone. Trenbolone acetate lacks a carbon atom at the 19 position and carries a double bond at carbons 9 and 11. The position of these carbons slows its metabolism, which greatly increases its binding affinity to the AR, and inhibits it from undergoing aromatization into the corresponding estrogenic metabolite. Trenbolone acetate contains trenbolone modified with the addition of a carboxylic acid ester ( acetic acid ) at the 17β-hydroxyl group.  This facilitates the slow release of the AAS from the area of injection.