Product Overview

Elbasvir is an active pharmaceutical ingredient (API) used in the development of antiviral drugs, widely applied in the innovative drug development for the treatment of hepatitis C. As a core intermediate or key starting material, elbasvir is suitable for all stages of drug synthesis, from research and development to small-scale preparation, pilot-scale amplification, and commercial production. Its high purity and stable chemical properties make it an important choice for pharmaceutical companies in process optimization and product development, meeting diverse application scenarios from laboratory to large-scale production.

Applications

• Antiviral drug synthesis
• Hepatitis C treatment drug development
• Drug intermediate supply
• Process route optimization and validation
• Customized pharmaceutical synthesis services

Quality & Supply Capability

English Name: Elbasvir Properties: This product is a white to off-white crystalline powder with good thermal and chemical stability. It contains a nitrogen-containing heterocyclic structure, is readily soluble in organic solvents, and is 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 sample supply, small-scale preparation, pilot-scale amplification, and customized batch production services. We can provide flexible supply solutions based on customer requirements for purity, impurity control, packaging specifications, delivery time, and quality documentation. Simultaneously, we provide comprehensive technical support from laboratory R&D to scale-up production, helping customers advance process development, route optimization, and project transformation, ensuring efficient and compliant product lifecycle management.

Why Choose Bioncan

Focused on APIs (Active Pharmaceutical Ingredients), possessing a rich product line and professional experience. Full-scale supply capabilities, covering all stages from laboratory to commercial production. Provide complete quality control documentation, complying with GMP and ICH standards. Support customized needs, flexibly addressing different customer application scenarios. Supporting process optimization technology and project scale-up services to help customers achieve technology transfer and product commercialization.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1370468-36-2, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.