Beclometasone Dipropionate Impurity – U
9,11β-epoxy-21-hydroxy-16β-methyl-3,20-dioxo-9βpregna-1,4-dien-17-yl propanoate
| Chemical Name | 9,11β-epoxy-21-hydroxy-16β-methyl-3,20-dioxo-9βpregna-1,4-dien-17-yl propanoate |
|---|---|
| CAS No. | 79578-39-5 |
| Molecular Formula | C25H32O6 |
| Molecular Weight | 428.53 |
| Chemical Structure |
 |
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Beclometasone Dipropionate Impurity – U
Beclometasone Dipropionate Impurity – U represents a known degradation or process impurity of Beclometasone Dipropionate in accordance with EP specifications. Chemically, it is described as 9,11β-epoxy-21-hydroxy-16β-methyl-3,20-dioxo-9βpregna-1,4-dien-17-yl propanoate. It has the molecular formula C25H32O6 and a molecular weight of 428.53 g/mol. It plays a key role in stability-indicating assay development and regulatory impurity profiling for Beclometasone Dipropionate. Available with a Certificate of Analysis (CoA) as a high-purity reference standard suitable for HPLC and LC-MS applications.
Beclometasone Dipropionate 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 Beclometasone Dipropionate 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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