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Methylprednisolone Impurity – E

11β-hydroxy-6α-methyl-3-oxoandrosta-1,4-diene-17βcarboxylic acid

Chemical Name 11β-hydroxy-6α-methyl-3-oxoandrosta-1,4-diene-17βcarboxylic acid
CAS No. 229019-44-7
Molecular Formula C21H28O4
Molecular Weight 344.45
Chemical Structure 11β-hydroxy-6α-methyl-3-oxoandrosta-1,4-diene-17βcarboxylic acid Structure
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Methylprednisolone Impurity – E

Methylprednisolone Impurity – E is identified as a process-related impurity of Methylprednisolone in accordance with EP specifications. Chemically, it is described as 11β-hydroxy-6α-methyl-3-oxoandrosta-1,4-diene-17βcarboxylic acid. It has the molecular formula C21H28O4 and a molecular weight of 344.45 g/mol. It serves as a critical reference material for identifying and quantifying related substances during Methylprednisolone manufacturing and stability testing. Available with a Certificate of Analysis (CoA) as a high-purity reference standard suitable for HPLC and LC-MS applications.

Methylprednisolone impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Methylprednisolone impurities that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related impurities.

This related products or Impurities are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.

BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.

BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.

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