N 3 Dimethylaminopropyl N Ethylcarbodiimide Hydrochloride, commonly known as EDAC or EDC HCl, represents a highly effective carbodiimide coupling agent specifically designed for fo...

N 3 Dimethylaminopropyl N Ethylcarbodiimide Hydrochloride, commonly known as EDAC or EDC HCl, represents a highly effective carbodiimide coupling agent specifically designed for forming amide bonds in organic and biochemical synthesis processes. With CAS number 25952-53-8 and molecular formula C8H17N3 · HCl, this compound features a molecular weight of 191.70 and falls under organic chemicals classification. The liquid appearance and medicinal grade standard ensure top-tier quality and reliability for demanding applications. The product maintains 100% purity with only 2% admixture, packaged in airtight containers to guarantee stability and extended shelf life. Its proven high effectiveness and absence of side effects make it a trusted choice for critical applications where precision and consistency are non-negotiable requirements.

This coupling agent finds extensive application across pharmaceutical manufacturing, biotechnology development, and research institutions. Within pharmaceutical production, it facilitates efficient peptide synthesis and advanced drug development, enabling the creation of complex therapeutic molecules. Biotechnology companies utilize it for protein conjugation processes and diagnostic assay production, ensuring accurate and reproducible results in sensitive applications. Research laboratories depend on it for molecular biology experiments including nucleic acid modifications and enzyme immobilization techniques. The medicinal grade standard makes it suitable for GMP-compliant environments, supporting industries that demand stringent quality controls and reliable performance in critical processes.

The business value of EDAC HCl lies in its exceptional reliability and operational efficiency, which significantly reduce processing risks while enhancing overall productivity. The high purity level and effectiveness minimize waste and rework requirements, leading to substantial cost savings and accelerated project timelines. The airtight, sturdy packaging ensures complete product integrity during storage and transportation, reducing spoilage risks and maintaining batch-to-batch consistency. Rigorous quality testing guarantees every batch meets exacting standards, providing complete confidence to procurement teams. These combined attributes make it an indispensable tool for organizations aiming to optimize synthesis processes, improve output quality, and maintain competitive advantage in demanding markets.

Key Features:
- High purity grade with 100% purity and minimal 2% admixture for reliable performance
- Medicinal grade standard suitable for pharmaceutical and biotechnology applications
- Liquid form ensuring easy handling and integration into various synthesis processes
- Airtight and sturdy packaging that maintains product stability and extends shelf life
- Quality tested with proven effectiveness and no side effects for consistent results

Benefits:
- High purity ensures reliable amide bond formation with minimal byproducts
- Medicinal grade compliance supports use in regulated manufacturing environments
- Liquid form simplifies handling and integration into synthesis workflows
- Secure packaging protects product integrity during storage and transportation
- Quality testing guarantees consistent performance and reduces operational risks