EDC Hydrochloride丨CAS 25952-53-8

EDC Hydrochloride丨CAS 25952-53-8
Product Introduction:
CAS No.: 25952-53-8
Product Name: EDC hydrochloride
Molecular Formula: C8H18ClN3
Molecular Weight: 191.70
Synonyms: 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
Send Inquiry
Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of edc hydrochloride丨cas 25952-53-8 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

High Purity EDC hydrochloride丨CAS 25952-53-8

 

EDC Hydrochloride, also known as 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC·HCl), is a water-soluble carbodiimide coupling reagent widely used in organic synthesis, peptide chemistry, and bioconjugation research. It activates carboxyl groups to facilitate the formation of amide bonds and other linkages under suitable reaction conditions. Its water compatibility makes it particularly valuable in aqueous coupling workflows, including protein modification, biomolecule conjugation, and surface functionalization.

 

Chemical Identifiers

 

InChI InChI=1S/C8H17N3.ClH/c1-4-9-8-10-6-5-7-11(2)3;/h4-7H2,1-3H3;1H
InChI Key FPQQSJJWHUJYPU-UHFFFAOYSA-N
Smiles CCN=C=NCCCN(C)C.Cl
EC No. 247-361-2
MDL No. MFCD00012503
PubChem CID 2723939

 

 

 

Applications

 

Peptide Synthesis and Amide Bond Formation

EDC Hydrochloride is commonly used to promote peptide bond formation and the coupling of carboxylic acids with amines. In peptide synthesis and related research, it supports the preparation of peptides, modified amino acids, and other amide-containing compounds. Reaction conditions and, where appropriate, coupling additives can be optimized to improve efficiency and limit unwanted side reactions.

Pharmaceutical Research and Drug Discovery

In pharmaceutical research, EDC Hydrochloride can support the synthesis of amide-containing intermediates, molecular conjugates, and specialized compounds for drug discovery. Researchers may use it during synthetic route development, molecular functionalization, and the preparation of structures for biological evaluation. Its suitability depends on the target molecule, substrate compatibility, and requirements for purification and impurity control.

Bioconjugation and Biomolecule Modification

EDC·HCl is widely applied in bioconjugation workflows that link carboxyl-containing molecules to compounds bearing primary amino groups. These reactions can support the preparation of protein conjugates, biomolecule-linked probes, and other research constructs. Its compatibility with aqueous reaction systems makes it useful for selected applications involving proteins and other biological materials, subject to appropriate control of pH and reaction conditions.

Surface Functionalization and Materials Science

EDC·HCl is used in selected materials research workflows to facilitate the attachment of molecules to carboxyl-functionalized surfaces or particles. It can support the preparation of functionalized polymers, biomaterial surfaces, and research materials designed for molecular recognition or immobilization studies. Applications may include laboratory investigations involving biosensors, separation materials, and surface-bound biomolecules.

 

 

 

Send Inquiry
Beyond Your Expectation
From Science to Life with LEAPChem
contact us