|Product Name||Methylprednisolone Acetate EP Impurity F|
|Synonyms||6α-Methyl-3,11,20-trioxopregna-1,4-dien-21-yl Acetate; 2-Oxo-2-((6S,8S,9S,10R,13S,14S)-6,10,13-trimethyl-3,11-dioxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)ethyl Acetate|
|Related API||Methylprednisolone Acetate|
Methylprednisolone Acetate EP Impurity F product with CAS number NA and catalog number SA25002 is related to Methylprednisolone Acetate. 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 Methylprednisolone Acetate.
Methylprednisolone is a corticosteroid medication used to suppress the immune system and decrease inflammation. methylprednisolone is typically used for its anti-inflammatory effects.
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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