Product Overview

1-Methylaurestatin E is an important pharmaceutical intermediate widely used in the synthesis of anti-tumor drugs, serving as a key structural unit. This product is primarily used in targeted drug development and the construction of antibody-drug conjugates (ADCs), suitable for various stages including research and development, pilot-scale, and large-scale production. Its high purity and stable chemical properties provide reliable assurance for subsequent process optimization and large-scale production, making it an essential raw material for pharmaceutical companies developing innovative drugs.

Applications

• Antitumor drug synthesis
• Antibody-drug conjugate (ADC) development
• Drug molecule structure modification and optimization
• Customized synthesis of pharmaceutical intermediates
• Innovative drug process development and route validation

Quality & Supply Capability

English Name: MonoMethyl auristatin E Properties: This product is a white to off-white solid with good chemical stability. It contains unique carbamate functional groups, making it suitable for various coupling reaction systems and meeting pharmaceutical-grade standards. 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 offer comprehensive technical support from laboratory research and development to scale-up production, helping customers advance process development, route optimization, and project transformation, ensuring efficient and compliant completion of the drug development process.

Why Choose Bioncan

Focused on pharmaceutical intermediates, with extensive experience in supplying API and ADC-related compounds. Full-scale supply capabilities to meet diverse needs from R&D to commercial production. Comprehensive quality control documentation to ensure product compliance with drug regulatory requirements in various countries. Customized synthesis and packaging solutions available to meet client needs. Supporting process optimization technologies to facilitate a smooth transition from laboratory to production.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 474645-27-7, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.