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Catalog Number:
33480
CAS Number:
1993176-75-2
N- (2-azidoacétyl)glycylglycine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Azidotriglycine, N -3-Gly-Gly-Gly-OH
Antibiotic
Documents
$127.79 /100 mg
Taille
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Informations sur le produit

N-(2-azidoacetyl)glycylglycine is a versatile compound that plays a significant role in various fields, particularly in biochemistry and medicinal chemistry. This compound, characterized by its azido group, is particularly valuable for researchers focusing on bioconjugation and click chemistry applications. Its unique structure allows for the selective labeling of biomolecules, making it an essential tool in the development of targeted drug delivery systems and imaging agents. The azido functionality enables efficient reactions with alkyne-containing compounds, facilitating the synthesis of complex molecular architectures that are crucial in pharmaceutical research.

In addition to its applications in drug development, N-(2-azidoacetyl)glycylglycine can also be utilized in the synthesis of peptide-based therapeutics and as a building block in the creation of novel biomaterials. Its ability to participate in bioorthogonal reactions enhances its utility in the design of smart materials that respond to biological stimuli. Researchers and industry professionals will find this compound particularly advantageous for its ease of use and the potential to streamline complex synthesis processes, ultimately accelerating the pace of innovation in drug discovery and development.

Numéro CAS 
1993176-75-2
Formule moléculaire
C6H9N5O4
Poids moléculaire 
215.2
Point de fusion 
150 - 154 °C
Informations générales
Numéro CAS 
1993176-75-2
Formule moléculaire
C6H9N5O4
Poids moléculaire 
215.2
Point de fusion 
150 - 154 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

N-(2-azidoacetyl)glycylglycine is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules like proteins or antibodies to various surfaces or carriers, enhancing drug delivery systems.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating targeted therapies that can selectively bind to specific cells, improving treatment efficacy.
  • Peptide Synthesis: This chemical is used in the synthesis of peptides, facilitating the incorporation of azide groups that can be further modified for various applications in medicinal chemistry.
  • Click Chemistry: As a part of click chemistry reactions, it enables the rapid and efficient formation of complex molecules, streamlining the development of new materials and therapeutics.
  • Diagnostic Tools: It is utilized in the development of diagnostic agents, particularly in imaging techniques, where its unique properties allow for enhanced visualization of biological processes.

Citations