Product Overview

Niraparib tosylate monohydrate is a key intermediate in the synthesis of the antitumor drug niraparib, widely used in the research and development and production of targeted therapies, suitable for research, pilot-scale, and large-scale production stages. This product exhibits excellent chemical stability and operability, meeting the stringent requirements of the pharmaceutical industry for high-purity, high-quality intermediates, providing customers with reliable raw material supply and process support.

Applications

• Synthetic precursor of the antitumor drug niraparib
• Drug molecular structure modification and optimization research
• Customized synthesis services for pharmaceutical intermediates
• Preclinical research and formulation development support
• Development and validation of innovative drug process routes

Quality & Supply Capability

English Name: Niraparib Tosylate Properties: White to off-white crystalline powder, readily soluble in organic solvents, with a stable aromatic sulfonate structure, suitable for various drug synthesis pathways. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches. Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging. Document Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust the supply plan according to the customer's specific requirements for purity, impurity control, packaging specifications, delivery cycle, and quality documents. Simultaneously, we have a professional technical support team to assist customers in completing process optimization and project transformation from laboratory R&D to large-scale production, ensuring product quality and delivery efficiency, and meeting the needs of scientific research and industrialization at different stages.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive experience and technical expertise in drug synthesis. Full-scale supply capabilities, covering all stages from laboratory to commercialization. Comprehensive quality control documentation support, including key data such as COA, HPLC, and NMR. Customization support available, enabling process adjustments and product optimization based on specific customer requirements. Comprehensive process optimization and scale-up technical support to help customers efficiently advance their R&D and production processes.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 1613220-15-7, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.