Desoxycorticosterone pivalate

Base Information

• Chemical Name: Desoxycorticosterone pivalate
• CAS No.: 808-48-0
• Molecular Formula: C26H38O4
• Molecular Weight: 414.585
• Hs Code.: 2937290000
• Mol file: 808-48-0.mol

Synonyms:11-Deoxycorticosterone,pivalate (8CI);Corticosterone, deoxy-, pivalate (6CI,7CI);Pivalic acid, esterwith 11-deoxycorticosterone (8CI);21-Hydroxypregn-4-ene-3,20-dione pivalate;Cortexone M;DOCP;DTMA;Deoxycorticosterone pivalate;Deoxycorticosteronetrimethylacetate;Deoxycortone pivalate;Deoxycortone trimethylacetate;Desoxycorticosterone pivalate;Desoxycorticosterone trimethylacetate;Desoxycortisone pivalate;Desoxycortone pivalate;NSC 95278;Neodin-Depositum;Percorten M;Percorten Pivalate;

Chemical Property of Desoxycorticosterone pivalate

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 198-204 °C
• Refractive Index: 1.534
• Boiling Point: 529.012 °C at 760 mmHg
• Flash Point: 225.517 °C
• PSA: 60.44000
• Density: 1.111 g/cm³
• LogP: 5.29290
• Storage Temp.: Refrigerator
• Solubility.: Chloroform (Slightly), Methanol (Slightly)

Purity/Quality:

98%,99%, ^*data from raw suppliers

11-DeoxyCorticosteronePivalate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Desoxycorticosterone pivalate is a mineralocorticoid hormone and an analog of desoxycorticosterone. 11-Deoxycorticosterone Pivalate is used in the treatment of adrenocortical insufficiency. It is used to treat in patients suffering from rheumatoid arthritis. 11-Deoxycorticosterone Pivalate is a mineralocorticoid hormone and an analog of desoxycorticosterone. 11-Deoxycorticosterone Pivalate is used in the treatment of adrenocortical insufficiency. It is used to treat in patients suffering from rheumatoid arthritis.

Technology Process of Desoxycorticosterone pivalate

There total 3 articles about Desoxycorticosterone pivalate 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:

→ deoxycorticosterone pivalate (808-48-0)

Guidance literature:

With acetone;

DOI:10.1002/hlca.19510340139

Reference yield:

17-hydroxyprogesterone (68-96-2) + pivaloyl chloride (3282-30-2) → deoxycorticosterone pivalate (808-48-0)

Guidance literature:

With pyridine;

DOI:10.1002/hlca.19510340139

Reference yield:

→ 21-Hydroxy-4-pregnen-3,20-diontrimethylacetat (808-48-0)

Guidance literature:

21-Hydroxy-4-pregnen-3,20-dion, Py., Trimethylessigsaeureanhydrid;

upstream raw materials:

17-hydroxyprogesterone

pivaloyl chloride