High Purity Pharmaceutical Intermediate CAS 1012341-50-2: Manufacturer & Supplier for Sacubitril Synthesis

Source high-quality Pharmaceutical Intermediate CAS 1012341-50-2, a critical building block for Sacubitril synthesis. We are a trusted manufacturer and supplier in China, offering superior purity and reliable supply for your pharmaceutical R&D and production needs. Get a quote for bulk purchase and ensure your supply chain stability.

Get a Quote & Sample

Key Advantages of Sourcing Our Pharmaceutical Intermediates

Exceptional Purity and Quality Control

Our Pharmaceutical Intermediate CAS 1012341-50-2 boasts a purity of ≥99%, with a specific specification of 99.5%. Each batch is rigorously tested to meet stringent quality standards, providing a reliable foundation for your pharmaceutical synthesis. We understand the critical role of purity in API manufacturing.

Strategic Importance in Pharmaceutical Synthesis

This intermediate is indispensable for the synthesis of Sacubitril, a cornerstone in modern heart failure treatment. By sourcing from us, you gain access to a critical precursor that supports the development of life-saving medications. Secure your supply of this vital chemical raw material.

Reliable Supply Chain and Manufacturing Expertise

As an experienced manufacturer in China, we guarantee a stable and consistent supply of Pharmaceutical Intermediate CAS 1012341-50-2. Our production processes are optimized for efficiency and quality, ensuring you can meet your manufacturing timelines without disruption. We are your trusted partner for bulk chemical sourcing.

Diverse Applications in Pharmaceutical Development

Active Pharmaceutical Ingredient (API) Synthesis

This intermediate serves as a fundamental building block for the synthesis of Active Pharmaceutical Ingredients (APIs), particularly in the development of cardiovascular drugs like Sacubitril. Its precise structure is key to the efficacy of the final API.

Research and Development

Essential for pharmaceutical research and development teams exploring novel therapeutic agents and optimizing existing synthesis routes. Its availability supports innovation in drug discovery and process chemistry.

Impurity Reference Standards

High-purity intermediates can also serve as crucial reference standards for identifying and quantifying impurities in the final drug product, ensuring regulatory compliance and patient safety.

Process Optimization Studies

Used in studies aimed at optimizing chemical synthesis processes, including exploring new catalysts, reaction conditions, and yield improvement strategies for Sacubitril and related compounds.