Prasterone enanthate

Base Information

• Chemical Name: Prasterone enanthate
• CAS No.: 23983-43-9
• Molecular Formula: C26H40O3
• Molecular Weight: 400.602
• European Community (EC) Number: 245-970-8
• UNII: 2W8I1S6T5L
• DSSTox Substance ID: DTXSID00946833
• Nikkaji Number: J242.714A
• Wikipedia: Prasterone_enanthate
• Wikidata: Q27255695
• Mol file: 23983-43-9.mol

Synonyms:dehydroepiandrosterone enanthate;DHEA oenanthate;SH 90300 D

Chemical Property of Prasterone enanthate

Chemical Property:

• Vapor Pressure: 4.76E-10mmHg at 25°C
• Melting Point: 69-70 °C
• Refractive Index: 1.528
• Boiling Point: 497.9 °C at 760 mmHg
• Flash Point: 211.4 °C
• PSA: 43.37000
• Density: 1.06 g/cm³
• LogP: 6.40050
• 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

(3S,8R,9S,10R,13S,14S)-10,13-Dimethyl-17-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ylHeptanoate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4=O)C)C
• Isomeric SMILES: CCCCCCC(=O)O[C@H]1CC[C@@]2([C@H]3CC[C@]4([C@H]([C@@H]3CC=C2C1)CCC4=O)C)C
• Uses: Prasterone Enanthate is used in preparation of DHEA enanthates for treating/improving adrenal hormonal balance, immune system function, adipose tissue reduction, skeletal muscle growth, bloating reduction, recovery from training, and increasing strength.
• Therapeutic Function: Glucocorticoid

Technology Process of Prasterone enanthate

There total 2 articles about Prasterone 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:

→ 3β-hydroxyandrost-5-en-17-one heptanoate (23983-43-9)

Guidance literature:

3β-Hydroxyandrost-5-en-17-on, Heptanoylchlorid;

Reference yield:

dehydroepiandrosterone (53-43-0) + Heptanoic acid chloride (2528-61-2) → DHEA enanthate (23983-43-9)

Guidance literature:

In toluene; Reflux;

DOI:10.2174/157018010791163505

upstream raw materials:

dehydroepiandrosterone

Heptanoic acid chloride

Refernces