Product Overview

Daclatasvir dihydrochloride is an important pharmaceutical intermediate widely used in the research and development and production of antiviral drugs, especially playing a key role in the synthesis of hepatitis C virus (HCV) treatments. This product is suitable for small-scale, pilot-scale, and large-scale production during the research and development phase, providing customers with stable, high-quality raw material support to meet the needs of process development and commercialization at different scales. It is a crucial basic material for pharmaceutical companies to optimize drug synthesis routes and validate processes.

Applications

• Antiviral drug synthesis
• Intermediates for hepatitis C treatment drugs
• Small-scale preparation in pharmaceutical R&D laboratories
• Pilot-scale process development and validation
• Optimization and improvement of drug process routes

Quality & Supply Capability

English Name: Daclatasvir dihydrochloride Properties: White to off-white crystalline powder, readily soluble in organic solvents, exhibiting good chemical stability. Contains a core amino and piperidine structure, suitable for various synthetic routes. Storage Recommendations: Store in a sealed, light-protected, and dry place, referring to the COA/MSDS for specific details. 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 flexibly adjust purity standards, impurity control requirements, packaging specifications, and delivery cycles according to customer needs, and provide complete quality documentation support. Simultaneously, we offer full-process technical support from laboratory R&D to scale-up production, helping customers achieve process development, route optimization, and project transformation, ensuring efficient and compliant project progress.

Why Choose Bioncan

Focused on the pharmaceutical intermediates field, possessing extensive industry experience and technological expertise. Full-scale supply capabilities, covering all stages from laboratory to commercial production. Provides complete quality control documentation to ensure controllable product quality and compliance with regulatory requirements. Flexible fulfillment of customized customer needs, including purity, impurity control, and packaging specifications. Supporting process optimization and scale-up technologies to help customers improve R&D efficiency and production conversion capabilities.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1009119-65-6, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.