651324-08-2 Oseltamivir Intermediates About
Presenting the affordable and top-tier Oseltamivir Intermediate (CAS No: 651324-08-2), featured for its resplendent purity (98%) and rigorous quality standards (In-house/USP). This pharmaceutical-grade intermediate is available in solid, odorless white to off-white powder, boasting stable, soaring performance and a glorious shelf life of two years. Expertly packed in HDPE drums with double PE bags (1kg, 5kg, 25kg customized), it dissolves effortlessly in DMSO, methanol, and ethanol. Every batch is identified and tested using IR, HPLC, and NMR, ensuring low impurity (1.0%), micronized availability, and strict compliance on all critical parameters-making it a leading choice for Oseltamivir Phosphate (Tamiflu) synthesis.
Site of Application and Material Excellence
The featured Oseltamivir Intermediate is primarily applied in pharmaceutical manufacturing for the synthesis of Oseltamivir Phosphate (Tamiflu)-a renowned anti-viral. Crafted to meet stringent international standards, its top physical forms and resplendent white-to-off-white appearance ensure consistent, dependable results. The material's principal feature lies in its high purity and excellent solubility, tailored for industry use. Ideal for drug formulation, this intermediate supports efficient synthesis processes and glorious end-product yield, proving its value to manufacturers worldwide.
Certifications, Delivery & Main Market Focus
Certified under both in-house and USP quality norms, our Oseltamivir Intermediate assures clients of premium product standards. We charge competitively for our supplies, serving an export market spanning China, India, and beyond. Delivery timelines are strictly maintained for reliable order fulfillment. Our main domestic market remains Asia, with prompt supply and logistical support designed for pharmaceutical companies needing timely, compliant intermediates in bulk. The glorious combination of quality and service underpins our soaring export performance.
FAQ's of 651324-08-2 Oseltamivir Intermediates:
Q: How can Oseltamivir Intermediate (651324-08-2) be identified for quality assurance?
A: Quality assurance is achieved through IR, HPLC, and NMR confirmation. Each batch is tested for optical rotation, purity, impurity, and physical characteristics to ensure compliance with in-house or USP standards.
Q: What is the primary usage of Oseltamivir Intermediate?
A: The intermediate is chiefly used in the synthesis of Oseltamivir Phosphate (Tamiflu), a widely administered anti-viral medication.
Q: When should Oseltamivir Intermediate be stored to maintain stability?
A: It is best stored in a cool, dry place with the container tightly closed to ensure stability and preserve its resplendent quality throughout its two-year shelf life.
Q: Where is the Oseltamivir Intermediate primarily supplied from?
A: This product is manufactured and exported from India, with an extensive supply network covering China and other regions globally.
Q: What is the benefit of using a pharmaceutical-grade intermediate with 98% purity?
A: Employing a pharmaceutical-grade intermediate of this purity guarantees a reliable and soaring yield in Tamiflu synthesis, reducing impurities and optimizing the quality of the final pharmaceutical product.
Q: How is Oseltamivir Intermediate shipped to ensure safety and product integrity?
A: The intermediate is securely packed in HDPE drums with double PE bags, available in 1kg, 5kg, and 25kg sizes to maintain safety and prevent contamination during transport.
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