Trenbolone-CAS:10161-33-8

Synonyms:

Estra-4,9,11-trien-3-one,17b-hydroxy- (7CI,8CI);(+)-Trenbolone;17b-Hydroxyestra-4,9,11-trien-3-one;17b-Trenbolone;9,10,11,12-Dehydro-19-nortestosterone;RU2341;Estra-4,9,11-trien-3-one,17-hydroxy-, (17b)-;Trienbolone;b-Trenbolone;Nandrolone Decanoate;

Canonical SMILES:

CC12C=CC3=C4CCC(=O)C=C4CCC3C1CCC2O

Isomeric SMILES:

C[C@]12C=CC3=C4CCC(=O)C=C4CC[C@H]3[C@@H]1CC[C@@H]2O

Description

Trenbolone, also known as trienolone or trienbolone, is a kind of anabolic androgenic steroid belonging to the 19-nortestosterone group. It can be supplied to veterinary medicine of livestock in order the boost muscle growth and appetite. It can also enhance the performance of athletes. It has several physiological effects: (1) enhance protein synthesis and nitrogen retention in the muscle tissues, which boost enhanced anabolism; (2) greatly promote insulin-like growth factor-1 (IGF-1) which is a highly effective anabolic hormone; (3) Greatly increase the red blood cell count to boost blood oxygenation which leads to improved muscular endurance; (4) Inhibit glucocorticoid hormones which inhibit the growth of muscle tissue and promote fat. (5) Improve food efficiency.

Uses

Trenbolone is a controlled substance (anabolic steroid). It is a steroid used on livestock to increase muscle growth and appetite. To increase its effective half-life, trenbolone is administered as a prodrug as an ester conjugate such as [trenbolone acetate], trenbolone enanthate, or trenbolone cyclohexylmethylcarbonate. Plasma lipases then cleave the ester group in the bloodstream leaving free trenbolone.

Technology Process of Trenbolone

There total 13 articles about Trenbolone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

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