Testosterone enanthate

Base Information

• Chemical Name: Testosterone enanthate
• CAS No.: 315-37-7
• Deprecated CAS: 11111-10-7
• Molecular Formula: C26H40O3
• Molecular Weight: 400.602
• Hs Code.: 2937290000
• European Community (EC) Number: 206-253-5
• NSC Number: 17591
• UNII: 7Z6522T8N9
• DSSTox Substance ID: DTXSID701016540
• Nikkaji Number: J5.664B
• Wikipedia: Testosterone_enanthate
• Wikidata: Q27108402
• NCI Thesaurus Code: C1247
• RXCUI: 37859
• Pharos Ligand ID: 6UHW35MJBY65
• Metabolomics Workbench ID: 35354
• ChEMBL ID: CHEMBL1200335
• Mol file: 315-37-7.mol

Synonyms:Andropository;Delatestryl;Durathate;Primoteston Depot;Testosteron Depot-Rotexmedica;Testosteron-Depot Eifelfango;Testosteron-Depot Jenapharm;testosterone enanthate;testosterone heptanoate;testosterone heptylate;Testrin P.A.;Theramex

Chemical Property of Testosterone enanthate

Chemical Property:

• Appearance/Colour: White crystalline powder
• Melting Point: 34-39 °C
• Refractive Index: 1.4700 (estimate)
• Boiling Point: 503.9 °C at 760 mmHg
• Flash Point: 214.2 °C
• PSA: 43.37000
• Density: 1.06 g/cm³
• LogP: 6.40050
• Storage Temp.: 2-8°C
• Solubility.: Practically insoluble in water, very soluble in anhydrous ethanol, freely soluble in fatty oils.
• XLogP3: 6.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 400.29774513
• Heavy Atom Count: 29
• Complexity: 679

Purity/Quality:

99% ^*data from raw suppliers

Testosterone enanthate United States Pharmacopeia (USP) Reference Standard ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 45-63
• Safety Statements: 53-22-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C
• Isomeric SMILES: CCCCCCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C
• Recent ClinicalTrials: Study of Testosterone and rHGH in FSHD
• Recent EU Clinical Trials: Short-term effects of testosterone enhantate and gel on neuro-physiological function
• Recent NIPH Clinical Trials: The effect of testosterone replacement on metabolism and QOL of the male patients with secondary hypogonadism
• Description: Testosterone enanthate (Item No. 22546) is an analytical reference standard categorized as an anabolic androgenic steroid. It is an ester of the naturally occurring androgen, testosterone (Item Nos. 15645 | ISO60154) with a longer half-life. Formulations containing testosterone enanthate have been tested for use in hypogonadism and as a potential male contraceptive. Formulations containing it have been associated with higher levels of total cholesterol, low density lipoproteins, and triglycerides and lower levels of high density lipoproteins. Anabolic steroids, including testosterone enanthate, have been used to enhance physical performance in racehorses and athletes, and methods to detect steroids, their derivatives, and their metabolites have been developed. This product is intended for research and forensic applications.
• Uses: Testosterone Enanthate is a derivative of testosterone (T155000), the principal hormone of the testes, produced by the interstitial cells.
• Therapeutic Function: Androgen

Technology Process of Testosterone enanthate

There total 15 articles about Testosterone enanthate 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: 97.18%

oenanthic acid (111-14-8) + 17β-hydroxy-3-methoxyandrosta-3,5-diene → testosterone heptanoate (315-37-7)

Guidance literature:

oenanthic acid; 17β-hydroxy-3-methoxyandrosta-3,5-diene; With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 40 ℃; Inert atmosphere;

With hydrogenchloride; In water;

Reference yield: 96.3%

oenanthic acid (111-14-8) + 17β-hydroxy-3-ethoxyandrosta-3,5-diene (26614-48-2,165304-83-6) → testosterone heptanoate (315-37-7)

Guidance literature:

oenanthic acid; 17β-hydroxy-3-ethoxyandrosta-3,5-diene; With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,2-dichloro-ethane; at 20 ℃; Inert atmosphere;

With sulfuric acid; In water;

Reference yield: 95.76%

oenanthic acid (111-14-8) + 3,3-(ethylenedioxy)-5-androsten-17β-ol (975-57-5) → testosterone heptanoate (315-37-7)

Guidance literature:

oenanthic acid; 3,3-(ethylenedioxy)-5-androsten-17β-ol; With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,2-dichloro-ethane; at 20 ℃; Inert atmosphere;

With sulfuric acid; In water;

upstream raw materials:

testosterone

Heptanoic acid chloride

3-ethoxyandrosta-3,5-dien-17-one

17β-hydroxy-3-ethoxyandrosta-3,5-diene

Downstream raw materials:

testosterone

6β-hydroxytestosterone

14alpha-Hydroxytestosterone

Androstenedione

Refernces

• 1、 -. "Synthesis method of alkyl acid testosterone". . . Retrieved 2020/12/10.