Product Overview

1-Methylaurestatin F is an important pharmaceutical intermediate widely used in the synthesis and development of anti-tumor drugs, especially in the field of antibody-drug conjugates (ADCs). As a key linker-drug component, this product is suitable for the entire process of drug development, small-scale preparation, pilot-scale amplification, and commercial production. Its high purity and stable chemical properties make it an important raw material for pharmaceutical companies to optimize processes and transform projects, meeting diverse needs from laboratory research to large-scale production.

Applications

• Antibody-Drug Conjugate (ADC) Synthesis
• Development of Antitumor Drug Intermediates
• Drug Molecular Structure Modification and Functionalization
• Customized Synthesis Services in Pharmaceutical R&D
• Process Route Optimization and Scale-up Production Support

Quality & Supply Capability

English Name: MonoMethylauristatin F Properties: This product is a white to off-white solid with good chemical stability. It contains ester and amino functional groups, making it suitable for various organic synthesis reactions and meeting the purity and impurity control standards for pharmaceutical intermediates. 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 Document Support: COA, MSDS, HPLC, NMR, etc. We provide comprehensive sample supply, small-scale preparation, pilot-scale amplification, and customized batch production services. 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 completing the entire process from laboratory research and development to large-scale production, promoting the smooth transformation and implementation of projects.

Why Choose Bioncan

Focused on pharmaceutical intermediates, with extensive experience in supplying APIs and key intermediates. Full-scale supply capabilities, covering all stages from laboratory to commercial production. Provides complete quality control documentation to ensure product quality compliance and controllability. Supports customized needs, adjusting purity, impurity limits, and packaging according to customer requirements. Provides process optimization and scale-up technical support to help customers improve R&D efficiency and production conversion rates.

Online Consulting

For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 745017-94-1, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.