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Mometasone Furoate Monohydrate Impurity – M

9-chloro-11β,17-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione

Chemical Name 9-chloro-11β,17-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione
CAS No. 57780-86-6
Molecular Formula C22H29ClO4
Molecular Weight 392.92
Chemical Structure 9-chloro-11β,17-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione Structure
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Mometasone Furoate Monohydrate Impurity – M

Mometasone Furoate Monohydrate Impurity – M is identified as a process-related impurity of Mometasone Furoate Monohydrate as per EP pharmacopoeial requirements. Chemically, it is described as 9-chloro-11β,17-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione. It has the molecular formula C22H29ClO4 and a molecular weight of 392.92 g/mol. It plays a key role in stability-indicating assay development and regulatory impurity profiling for Mometasone Furoate Monohydrate. Available as a high-purity certified reference material suitable for HPLC, LC-MS, and other analytical techniques.

Mometasone Furoate Monohydrate 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 Mometasone Furoate Monohydrate 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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