Product Overview

Oseltamivir is an important antiviral active pharmaceutical ingredient (API) primarily used for the prevention and treatment of influenza viruses, and is widely applied in pharmaceutical research and development and manufacturing. As a neuraminidase inhibitor, its core mechanism of action is well-defined, making it suitable for intervention against various influenza virus strains. This product supports the entire supply chain from laboratory research and development, small-scale trials to pilot-scale amplification and commercial production, meeting the process development and quality control requirements at different stages. It is an important raw material choice for pharmaceutical companies and custom synthesis service providers.

Applications

• Research and development and production of influenza vaccines and antiviral drugs
• Synthesis and preparation of antiviral drug intermediates
• Procurement of active pharmaceutical ingredients and formulation process development for pharmaceutical companies
• Customized synthesis services and process route optimization
• Drug registration application and quality standard establishment

Quality & Supply Capability

English Name: Oseltamivir Properties: This product is a white to off-white crystalline powder with good chemical stability. Its main functional group is a carboxylic acid ester structure. It is readily soluble in organic solvents and suitable for various synthetic routes. Storage Recommendations: Store in a sealed, light-protected, and dry place, referring to the COA/MSDS for specific requirements. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide comprehensive sample supply, small-scale preparation, pilot-scale amplification, and customized batch production services. We can flexibly adjust the supply plan according to customer requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documentation. We also provide technical support from laboratory R&D to scale-up production, helping customers advance process development, route optimization, and project transformation, ensuring stable product quality and compliance with regulatory requirements.

Why Choose Bioncan

Focused on antiviral active pharmaceutical ingredients (APIs), possessing extensive R&D and manufacturing experience. Full-scale supply capabilities, covering all stages from laboratory to commercialization. Provides complete quality control documentation, including COA, MSDS, HPLC, NMR, etc. Supports customized needs, enabling process adjustments and product optimization based on specific customer requirements. Supports scale-up technology to help customers smoothly transition from R&D to mass production.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 196618-13-0, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.