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Cortisone Acetate Impurity – A

11β,17-dihydroxy-3,20-dioxopregn-4-en-21-yl acetate (hydrocortisone acetate)

Chemical Name 11β,17-dihydroxy-3,20-dioxopregn-4-en-21-yl acetate (hydrocortisone acetate)
CAS No. 50-03-3
Molecular Formula C23H32O6
Molecular Weight 404.5
Chemical Structure 11β,17-dihydroxy-3,20-dioxopregn-4-en-21-yl acetate (hydrocortisone acetate) Structure
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Cortisone Acetate Impurity – A

Cortisone Acetate Impurity – A is documented as a related substance of Cortisone Acetate in pharmaceutical quality control as per EP pharmacopoeial requirements. Chemically, it is described as 11β,17-dihydroxy-3,20-dioxopregn-4-en-21-yl acetate (hydrocortisone acetate). It has the molecular formula C23H32O6 and a molecular weight of 404.5 g/mol. It serves as a critical reference material for identifying and quantifying related substances during Cortisone Acetate manufacturing and stability testing. Available as a high-purity certified reference material suitable for HPLC, LC-MS, and other analytical techniques.

Cortisone 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 Cortisone 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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