|Product Name||Betamethasone Valerate EP Impurity A|
|Synonyms||9-Fluoro-11β,17,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione; (11β,16β)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione; 9α-Fluoro-16β-methylprednisolone; Betadexamethasone; Flubenisolone ;(8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydroxy-17-(2-hydro,7,8,9,10,11,12,13,14,15,16,17-dpenta[a]phenanthren-17-yl pentanoate|
|Related API||Betamethasone Valerate|
Betamethasone Valerate EP Impurity A product with CAS number 378-44-9 and catalog number SA18500 is related to Betamethasone Valerate. This product is used for Abbreviated New Drug Application (ANDA) filing to FDA as well as for Quality Control (QC), toxicity studies and other analytical studies during commercial production of Betamethasone Valerate.
Betamethasone Valerate is a medication used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Betamethasone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a medium-strength corticosteroid.
All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity 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 is for research and development (R&D) use only.
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