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Catalog Number:
30456
CAS Number:
1454334-76-9
Chlorhydrate de N ε -Azido-L-Lysine
Purity:
≥ 99 % (dosage par titration, HPLC)
Synonym(s):
Chlorhydrate de ( S )-6-azido-2-amino-hexanoïque, Chlorhydrate de 6-azido-L-norleucine
Documents
$83.32 /100 mg
Taille
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Informations sur le produit

Ne-Azido-L-Lysine hydrochloride is a versatile amino acid derivative that plays a significant role in biochemical research and applications. This compound, characterized by its azido group, is particularly valuable in bioconjugation and click chemistry, enabling researchers to create complex biomolecules with precision. Its unique structure allows for selective labeling and modification of proteins, making it an essential tool in the development of targeted therapeutics and diagnostic agents.

In addition to its applications in drug development, Ne-Azido-L-Lysine hydrochloride is also utilized in the synthesis of peptide-based materials and in the study of protein interactions. Its ability to facilitate the introduction of functional groups into biomolecules opens up new avenues for research in areas such as proteomics and molecular biology. With its robust properties and practical applications, this compound is an indispensable resource for researchers looking to advance their work in chemical biology and related fields.

Numéro CAS 
1454334-76-9
Formule moléculaire
C6H13ClN4O2
Poids moléculaire 
208.6
Point de fusion 
163 - 176 ?C
Rotation optique 
[a] D 20 = 14,0 - 16,5 ° (C = 1 dans H 2 O)
Informations générales
Numéro CAS 
1454334-76-9
Formule moléculaire
C6H13ClN4O2
Poids moléculaire 
208.6
Point de fusion 
163 - 176 ?C
Rotation optique 
[a] D 20 = 14,0 - 16,5 ° (C = 1 dans H 2 O)
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

Ne-Azido-L-Lysine hydrochloride is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile building block for bioconjugation, allowing researchers to attach various biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Protein Labeling: It is employed in the labeling of proteins for visualization and tracking in cellular studies, making it easier to study protein interactions and functions in live cells.
  • Click Chemistry: The azide group in this compound is ideal for click chemistry applications, facilitating the rapid and selective formation of covalent bonds, which is crucial in drug development and materials science.
  • Peptide Synthesis: It is utilized in the synthesis of modified peptides, enabling the incorporation of azide functionality for further chemical modifications, thus expanding the toolbox for peptide research.
  • Biomedical Research: This compound is valuable in the development of novel therapeutic agents, particularly in cancer research, where targeted delivery systems can be enhanced through its unique chemical properties.

Citations