The Importance of 98% Purity 3-Oxo Atorvastatin for Pharma
In the pharmaceutical industry, the adage 'purity matters' holds particularly true. For compounds like 3-Oxo Atorvastatin (CAS 887196-30-7), a critical player in the Atorvastatin synthesis and quality control landscape, achieving and maintaining high purity levels is non-negotiable. This specific impurity/intermediate, with its molecular formula C33H33FN2O5 and molecular weight of 556.62 g/mol, demands meticulous manufacturing processes to meet the exacting standards of drug development and production.
The significance of 3-Oxo Atorvastatin lies in its dual nature. Firstly, it is a known impurity generated during the synthesis of Atorvastatin calcium, a widely prescribed statin. Regulatory bodies worldwide, including the EP and USP, set stringent limits for such impurities in pharmaceutical products. To effectively monitor and control these levels, pharmaceutical companies require highly pure 3-Oxo Atorvastatin as a reference standard. This standard is crucial for validating analytical methods, such as HPLC and LC-MS, ensuring they can accurately detect and quantify the impurity in the final API. A purity of 98% is generally the minimum requirement for such analytical applications, providing a reliable benchmark for quality control.
Secondly, 3-Oxo Atorvastatin is also a valuable pharmaceutical intermediate. Researchers and chemists utilize it in various aspects of drug development. This includes studying the degradation pathways of Atorvastatin, investigating its metabolic profile, and exploring novel synthetic strategies. For these R&D efforts, the purity of the starting material directly impacts the validity and reproducibility of experimental results. Using a precisely characterized compound ensures that any observed effects are attributable to the substance itself, not to confounding impurities.
Many pharmaceutical professionals actively seek to buy 3-oxo atorvastatin manufacturer China due to the region's robust chemical manufacturing capabilities and competitive pricing. As a dedicated manufacturer of 3-Oxo Atorvastatin, we specialize in producing this compound to the highest purity standards, consistently achieving 98% or greater. Our commitment to quality is reflected in our comprehensive quality control processes and the detailed analytical data provided with each product. We aim to be a trusted pharmaceutical intermediate supplier for clients globally.
When considering the procurement of such specialized chemicals, understanding the supplier's capabilities is paramount. Whether you need gram quantities for research or kilogram amounts for pilot-scale production, a reliable supplier in China can offer both quality and cost-effectiveness. We understand the importance of timely delivery and consistent product quality for your critical projects. Therefore, we encourage you to order 3-oxo atorvastatin from us, knowing you are receiving a product that meets the stringent demands of the pharmaceutical industry.
In conclusion, the 98% purity of 3-Oxo Atorvastatin is not merely a specification but a critical enabler for pharmaceutical quality control, regulatory compliance, and cutting-edge research. By partnering with an experienced and quality-focused manufacturer, you can ensure that you have access to this vital compound, facilitating the development and production of safe and effective medications. We offer competitive pricing for 3-oxo atorvastatin and are ready to discuss your specific needs.
Perspectives & Insights
Alpha Spark Labs
“This specific impurity/intermediate, with its molecular formula C33H33FN2O5 and molecular weight of 556.”
Future Pioneer 88
“62 g/mol, demands meticulous manufacturing processes to meet the exacting standards of drug development and production.”
Core Explorer Pro
“Firstly, it is a known impurity generated during the synthesis of Atorvastatin calcium, a widely prescribed statin.”