Hydrocortisone 16, 17-hydro-17- carboxylic acid

CAS No. : 2394-25-4
Mol F. : C20H28O4
Mol W. : 332.43
Cat No. : SA15224
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Description

Product NameHydrocortisone 16, 17-hydro-17-
carboxylic acid
Synonyms17-Deoxy Cortienic Acid

11β-Hydroxy-3-oxo-androst-4-ene-17β-carboxylic Acid

(8S,9S,10R,11S,13S,14S,17S)-11-
hydroxy-10,13-dimethyl-3-oxo-
2,3,6,7,8,9,10,11,12,13,14,15,16,17-
tetradecahydro-1Hcyclopenta[
a]phenanthrene-17-
carboxylic acid

Related APIHydrocortisone
CategoryImpurities

Hydrocortisone 16, 17-hydro-17-
carboxylic acid product with CAS: 2394-25-4 is also known as 17-Deoxy Cortienic Acid; 11β-Hydroxy-3-oxo-androst-4-ene-17β-carboxylic Acid. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). Hydrocortisone 16, 17-hydro-17-
carboxylic acid is used in Hydrocortisone impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines during commercial production of Hydrocortisone and its related formulations. Moreover, 17-Deoxy Cortienic Acid is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Hydrocortisone developed in our R&D.

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Certificate of Analysis (CoA) and Characterization Data:

All products are provided with a certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS, etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). 

This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.

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