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Catalog Number:
33479
CAS Number:
855750-87-7(net)
N-(2-azidoacetyl)glycine·DCHA salt
Purity:
>98%
Synonym(s):
Azido diglycine dicyclohexylamine salt, N3-Gly-Gly-OH·DCHA
Antibiotic
Documents
$65.40 /100MG
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Product Information

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.

Synonyms
Azido diglycine dicyclohexylamine salt, N3-Gly-Gly-OH·DCHA
CAS Number
855750-87-7(net)
Purity
>98%
Molecular Formula
C4H6N4O3·C12H23N
Molecular Weight
339.4
MDL Number
MFCD31720295
Melting Point
162 - 165 ?C (Dec.)
Appearance
White crystalline powder
Conditions
Store at 2-8 °C
General Information
Synonyms
Azido diglycine dicyclohexylamine salt, N3-Gly-Gly-OH·DCHA
CAS Number
855750-87-7(net)
Purity
>98%
Molecular Formula
C4H6N4O3·C12H23N
Molecular Weight
339.4
MDL Number
MFCD31720295
Melting Point
162 - 165 ?C (Dec.)
Appearance
White crystalline powder
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
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