Medroxyprogestrone Acetate EP Impurity F
|CAS No.||: 69688-15-9|
|Mol F.||: C24H36O4|
|Mol W.||: 388.54|
|Cat No.||: SA27805|
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|Product Name||Medroxyprogestrone Acetate EP Impurity F|
|Synonyms||4,5-Dihydro Medroxyprogesterone Acetate|
Medroxyprogesterone Acetate USP RC A
(5β)-4,5-Dihydro Medroxy Progesterone 17-Acetate
|Related API||Medroxyprogesterone Acetate|
Medroxyprogestrone Acetate EP Impurity F product with CAS: 69688-15-9 is also known as 4,5-Dihydro Medroxyprogesterone Acetate; Medroxyprogesterone Acetate USP RC A. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). Medroxyprogestrone Acetate EP Impurity F is used in Medroxyprogesterone Acetate impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines during commercial production of Medroxyprogesterone Acetate and its related formulations. Moreover, 4,5-Dihydro Medroxyprogesterone Acetate 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 Medroxyprogesterone Acetate 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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