The Role of 3-Oxo Atorvastatin in Pharmaceutical Quality Control
In the stringent landscape of pharmaceutical manufacturing, the control and monitoring of impurities are paramount to ensuring drug safety and efficacy. 3-Oxo Atorvastatin (CAS 887196-30-7) plays a significant role in this process, particularly concerning Atorvastatin, a cornerstone medication in managing hypercholesterolemia. As a recognized impurity and a valuable pharmaceutical intermediate, its availability in high purity is crucial for regulatory compliance and robust quality assurance.
Atorvastatin, a highly effective statin, requires precise manufacturing processes. During its synthesis, 3-Oxo Atorvastatin can arise as a byproduct. Its chemical identity is C33H33FN2O5, with a molecular weight of 556.62. Regulatory bodies worldwide, including those that formulate the European Pharmacopoeia (EP) and United States Pharmacopeia (USP), mandate strict limits on impurities in pharmaceutical products. For instance, 3-Oxo Atorvastatin is designated as Impurity O in the EP monograph for Atorvastatin Calcium. Meeting these pharmacopoeial standards necessitates reliable access to this specific impurity as a reference standard.
Pharmaceutical quality control (QC) departments depend on accurate reference standards to develop and validate analytical methods. Techniques like High-Performance Liquid Chromatography (HPLC) and Ultra-Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS/MS) are employed to detect and quantify 3-Oxo Atorvastatin at trace levels in Atorvastatin drug substances and products. A high-purity standard ensures that these analytical methods are sensitive, specific, and reproducible. Therefore, sourcing from a trusted impurity standard manufacturer is not merely a procedural step but a fundamental requirement for ensuring product quality.
Beyond its role as an impurity, 3-Oxo Atorvastatin also serves as a pharmaceutical intermediate. Researchers utilize it to study the degradation pathways of Atorvastatin, understand its metabolic fate, and explore novel synthetic strategies. For companies involved in these research and development activities, consistent access to this compound is vital. Many research institutions and pharmaceutical manufacturers actively search to buy 3-oxo atorvastatin manufacturer China, recognizing the region's expertise in fine chemical production and its capacity to supply such specialized compounds.
As a leading manufacturer and supplier of 3-Oxo Atorvastatin in China, we are dedicated to supporting the pharmaceutical industry’s needs. We offer this compound with a guaranteed purity of 98%, providing the reliability and precision required for critical quality control applications. Our goal is to be your go-to pharmaceutical intermediate supplier, ensuring that you have access to the materials necessary for drug development and manufacturing. When you are ready to order 3-oxo atorvastatin, consider the advantages of partnering with an experienced and quality-focused supplier.
In summary, 3-Oxo Atorvastatin is more than just a chemical compound; it is an essential component in maintaining the integrity and quality of Atorvastatin-based pharmaceuticals. Its dual role as an impurity and an intermediate underscores the importance of reliable sourcing. For competitive pricing for 3-oxo atorvastatin and consistent quality, we invite you to engage with us, your trusted global partner for specialized pharmaceutical chemicals.
Perspectives & Insights
Agile Reader One
“For competitive pricing for 3-oxo atorvastatin and consistent quality, we invite you to engage with us, your trusted global partner for specialized pharmaceutical chemicals.”
Logic Vision Labs
“In the stringent landscape of pharmaceutical manufacturing, the control and monitoring of impurities are paramount to ensuring drug safety and efficacy.”
Molecule Origin 88
“3-Oxo Atorvastatin (CAS 887196-30-7) plays a significant role in this process, particularly concerning Atorvastatin, a cornerstone medication in managing hypercholesterolemia.”