Product Overview

Taltobulin is an important pharmaceutical intermediate widely used in the synthesis of anti-tumor drugs, exhibiting excellent reactivity and structural stability. This product is suitable for various stages of drug development, from small-scale preparation to pilot-scale amplification and commercial production, serving as a key raw material for constructing specific drug molecular skeletons. Its high purity and reliable supply capacity can meet the diverse needs of customers in process development, route optimization, and project transformation, helping pharmaceutical companies efficiently advance the process of new drug research and development and industrialization.

Applications

• Antitumor drug synthesis
• Drug molecule skeleton construction
• Process development and route optimization
• Pilot-scale production and commercial production
• Customized intermediate synthesis

Quality & Supply Capability

English Name: Taltobulin Properties: Taltobulin is a white to off-white crystalline powder with a stable chemical structure. It is readily soluble in common organic solvents, suitable for various organic synthesis reactions, and exhibits good thermal and storage stability. 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 Document Support: COA, MSDS, HPLC, NMR, etc. We provide comprehensive supply services from laboratory samples to industrial-scale production. We can flexibly adjust purity standards, impurity control requirements, packaging specifications, and delivery cycles according to customer needs to ensure product compliance with GMP and industry standards. Simultaneously, we have a professional technical team that can provide customers with full-process technical support from experimental research to process scale-up, helping customers achieve efficient, safe, and compliant drug development and production.

Why Choose Bioncan

Focused on pharmaceutical intermediates, possessing extensive synthesis experience and technological expertise. Full-scale supply capability, covering all stages from laboratory to commercial production. Provides complete quality testing documentation, including COA, MSDS, HPLC, NMR, etc. Supports customized needs, enabling process adjustments and product customization based on specific customer requirements. Comprehensive process optimization and scale-up technical support to improve customer R&D efficiency and production conversion rates.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 228266-40-8, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.