Trenbolone acetate

Base Information

• Chemical Name: Trenbolone acetate
• CAS No.: 10161-34-9
• Molecular Formula: C20H24O3
• Molecular Weight: 312.409
• Hs Code.: 2937290000
• European Community (EC) Number: 233-432-5
• UNII: RUD5Y4SV0S
• DSSTox Substance ID: DTXSID2046626
• Nikkaji Number: J15.597G
• Wikipedia: Trenbolone_acetate
• Wikidata: Q27288295
• NCI Thesaurus Code: C61982
• RXCUI: 1484277
• Metabolomics Workbench ID: 155020
• ChEMBL ID: CHEMBL1698011
• Mol file: 10161-34-9.mol

Synonyms:17 beta-acetoxyestra-4,9,11-trien-3-one;Acetate, Trenbolone;Acetate, Trienbolone;Progro T S;Progro T-S;Progro TS;Trenbolone;trenbolone acetate;trenbolone acetate, (17beta)-isomer;Trienbolone;trienbolone acetate

Chemical Property of Trenbolone acetate

Chemical Property:

• Appearance/Colour: yellow or yellow-white crystalline powder
• Vapor Pressure: 1.26E-09mmHg at 25°C
• Melting Point: 90-92°C
• Refractive Index: 1.576
• Boiling Point: 486.7 °C at 760 mmHg
• Flash Point: 214.7 °C
• PSA: 43.37000
• Density: 1.18 g/cm³
• LogP: 3.90010
• Storage Temp.: 0-6°C
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 312.17254462
• Heavy Atom Count: 23
• Complexity: 666

Purity/Quality:

99% ^*data from raw suppliers

Trenbolone acetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 60
• Safety Statements: 22-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1CCC2C1(C=CC3=C4CCC(=O)C=C4CCC23)C
• Isomeric SMILES: CC(=O)O[C@H]1CC[C@@H]2[C@@]1(C=CC3=C4CCC(=O)C=C4CC[C@@H]23)C
• Description: Trenbolone Acetate, a synthetic anabolic-androgenic steroid belonging to the nandrolone group, is structurally derived from estra-4,9,11-trien-17β-ol-3-one. It exists in various esterified forms, including trenbolone acetate, trenbolone hexahydrobenzylcarbonate, and trenbolone enanthate. Crystallographic studies have elucidated the structural features of these esters, revealing their monoclinic crystal structures with specific space groups. The steroid skeleton rings adopt distorted envelope and intermediate sofa half-chair configurations, with the D ring existing in a 13β distorted envelope configuration. ^[1]
• Used in Pharmaceutical Industries: Trenbolone Acetate is utilized as an anabolic agent to promote skeletal muscle growth and increase efficiency in the treatment of various medical conditions. Additionally, it serves as a valuable component in the development of performance-enhancing drugs.
• Used in Livestock Industries: In the livestock industry, trenbolone acetate is commonly employed to enhance the growth performance of beef cattle. It promotes increased average daily gain, gain-to-feed ratio, and carcass weight, thereby improving the overall productivity and profitability of beef production operations. Furthermore, trenbolone acetate plays a crucial role in promoting proliferation rate and influencing gene expression in bovine satellite cells, contributing to the optimization of muscle growth and development in cattle.^[2],^[1]
• References: [1] Structural studies of Trenbolone, Trenbolone Acetate, Hexahydrobenzylcarbonate and Enanthate esters; DOI 10.1016/j.molstruc.2020.128127; [2] Understanding the influence of trenbolone acetate and polyamines on proliferation of bovine satellite cells; DOI 10.1016/j.domaniend.2020.106479; [3] Effect of trenbolone acetate, melengestrol acetate, and ractopamine hydrochloride on the growth performance of beef cattle; DOI 10.1139/cjas-2020-0159

Technology Process of Trenbolone acetate

There total 1 articles about Trenbolone acetate 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:

synthetic route:

Reference yield:

→ 17β-hydroxyestra-4,9,11-trien-3-one 17-acetate (10161-34-9,49707-37-1)

Guidance literature:

entspr. Hydroxy-Verb. (VI), Essigsaeure;