Dexamethasone Acetate Impurity – A
9-fluoro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione (dexamethasone)
| Chemical Name | 9-fluoro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione (dexamethasone) |
|---|---|
| CAS No. | 50-02-2 |
| Molecular Formula | C22H29FO5 |
| Molecular Weight | 392.47 |
| Chemical Structure |
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Dexamethasone Acetate Impurity – A
Dexamethasone Acetate Impurity – A is documented as a related substance of Dexamethasone Acetate in pharmaceutical quality control as per EP pharmacopoeial requirements. Chemically, it is described as 9-fluoro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione (dexamethasone). It has the molecular formula C22H29FO5 and a molecular weight of 392.47 g/mol. Laboratories use this reference standard for impurity identification, method validation, and batch release testing related to Dexamethasone Acetate. Offered as a high-purity analytical reference standard for use in HPLC, LC-MS/MS, and other chromatographic techniques.
Dexamethasone Acetate 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 Dexamethasone Acetate 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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