Product Overview

Leadipasvir acetone solvate is a key pharmaceutical intermediate used in the development of antiviral drugs, primarily for the synthesis of the direct-acting antiviral drug ledipasvir. It is widely used in the preparation of drugs for treating hepatitis viruses (especially hepatitis C). This product is suitable for early-stage drug development, small-scale trials, pilot-scale amplification, and commercial production. It exhibits good chemical stability and high reactivity, meeting the needs of process development at different scales and providing customers with efficient and reliable raw material support.

Applications

• Synthesis of antiviral drug intermediates
• Process development of ledipasvir API
• Drug molecule structure modification and optimization
• Customized synthesis services for pharmaceutical companies
• Key starting materials in new drug development

Quality & Supply Capability

English Name: Ledipasvir (acetone) Properties: This product is a white to off-white crystalline powder with good thermal and chemical stability. It contains a specific acetone solvation structure, making it suitable for subsequent drug synthesis processes. 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 a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust the supply plan according to customer requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documentation. Simultaneously, we have a professional technical support team to assist customers in process development, route optimization, and project transformation, ensuring a stable supply and high-quality delivery of products at different stages.

Why Choose Bioncan

Focused on pharmaceutical nucleosides and pharmaceutical intermediates, possessing extensive industry experience. Full-scale supply capabilities, covering needs from laboratory to commercial production. Provides complete quality control documentation support, including key data such as COA, HPLC, and NMR. Supports customized needs, adjusting purity, impurity standards, and packaging according to customer requirements. Provides supporting process optimization and project scale-up technologies to help customers achieve efficient commercialization.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1441674-54-9, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.