Procuring High-Quality Rosuvastatin Intermediate R1: A Buyer's Guide
For procurement professionals and R&D scientists in the pharmaceutical sector, sourcing critical intermediates is a meticulous process. When it comes to the synthesis of Rosuvastatin, a cornerstone medication for cardiovascular health, obtaining the right intermediates with precise specifications is non-negotiable. This guide focuses on tert-Butyl 6-[(1E)-2-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetate, identified by CAS 289042-12-2, and provides insights for buyers seeking to purchase this essential compound.
The primary concern for any buyer of this Rosuvastatin intermediate R1 is its purity. High-purity materials, typically assayed at ≥99.0% by HPLC, are crucial for ensuring the success of subsequent synthesis steps and the quality of the final API. Beyond overall purity, attention must be paid to the impurity profile. Low levels of single impurities (e.g., < 0.3%) and total impurities (e.g., < 0.5%) are critical indicators of a well-controlled manufacturing process. The physical appearance, usually a white to off-white powder, also serves as an initial quality check.
When evaluating suppliers, particularly those based in China, buyers should prioritize manufacturers with a proven track record in pharmaceutical intermediate production. Key criteria include the ability to provide comprehensive Certificates of Analysis (CoA) that detail analytical methods and results, evidence of robust quality management systems (like ISO certifications), and a capacity for consistent supply. Furthermore, understanding the manufacturer's pricing structure and their responsiveness to inquiries is important for establishing a productive working relationship.
The benefits of sourcing from Chinese manufacturers for this intermediate are manifold. They often offer competitive pricing due to economies of scale and specialized production capabilities. Moreover, their extensive experience in chemical synthesis means they can reliably produce high-quality materials like CAS 289042-12-2, supporting the global pharmaceutical industry's demand. For procurement teams looking to buy Rosuvastatin intermediate R1, engaging with established Chinese suppliers like NINGBO INNO PHARMCHEM CO.,LTD. can lead to a more streamlined and cost-effective procurement process.
In conclusion, a successful procurement strategy for tert-Butyl 6-[(1E)-2-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetate involves a thorough assessment of product specifications, supplier reliability, and cost-effectiveness. By focusing on these key aspects, pharmaceutical companies can secure the high-quality intermediates necessary for efficient and compliant Rosuvastatin API manufacturing.
Perspectives & Insights
Data Seeker X
“The physical appearance, usually a white to off-white powder, also serves as an initial quality check.”
Chem Reader AI
“When evaluating suppliers, particularly those based in China, buyers should prioritize manufacturers with a proven track record in pharmaceutical intermediate production.”
Agile Vision 2025
“Key criteria include the ability to provide comprehensive Certificates of Analysis (CoA) that detail analytical methods and results, evidence of robust quality management systems (like ISO certifications), and a capacity for consistent supply.”