Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
33479
CAS Number:
855750-87-7
Sel de N- (2-azidoacétyl)glycine·DCHA
Purity:
>98%
Synonym(s):
Sel d'azido-diglycine-dicyclohexylamine, N3-Gly-Gly-OH·DCHA
Antibiotic
Documents
$65.40 /100 mg
Taille
Request Bulk Quote
Informations sur le produit

N-(2-azidoacetyl)glycine·DCHA salt is a versatile compound that has garnered attention in various fields, particularly in medicinal chemistry and bioconjugation applications. This compound, also known as 2-[(2-azidoacetyl)amino]acetic acid, features a unique azido group that enables it to participate in click chemistry reactions, making it an invaluable tool for researchers looking to create complex molecular structures efficiently. Its ability to form stable conjugates with biomolecules allows for innovative approaches in drug development, targeted delivery systems, and the synthesis of novel materials.

The DCHA salt form enhances the compound's solubility and stability, making it suitable for a range of laboratory applications. Researchers can leverage its properties for the development of bioconjugates, which are essential in the creation of targeted therapies and diagnostics. Additionally, its potential use in the synthesis of peptide-based drugs highlights its relevance in pharmaceutical research. With its unique reactivity and stability, N-(2-azidoacetyl)glycine·DCHA salt stands out as a valuable asset for professionals seeking to advance their work in chemical biology and related fields.

Numéro CAS 
855750-87-7
Formule moléculaire
C4H6N4O3 · C12H23N
Poids moléculaire 
339.4
Point de fusion 
162 - 165 °C (déc.)
Informations générales
Numéro CAS 
855750-87-7
Formule moléculaire
C4H6N4O3 · C12H23N
Poids moléculaire 
339.4
Point de fusion 
162 - 165 °C (déc.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

N-(2-azidoacetyl)glycine·DCHA salt is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation reactions, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing drug delivery systems.
  • Click Chemistry: Its azide functional group makes it ideal for click chemistry applications, facilitating the rapid and selective formation of covalent bonds, which is beneficial in developing new materials and pharmaceuticals.
  • Peptide Synthesis: The compound is used in the synthesis of modified peptides, providing unique functionalities that can improve stability and efficacy in therapeutic applications.
  • Diagnostic Applications: It can be employed in the development of diagnostic agents, where its ability to form stable complexes with target biomolecules enhances the sensitivity and specificity of detection methods.
  • Research in Medicinal Chemistry: The compound is valuable in medicinal chemistry for designing new drugs, particularly in targeting specific biological pathways due to its unique structural properties.

Citations