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Catalog Number:
30513
CAS Number:
333366-32-8
Nα- Azido - -Boc-L-Lysine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide ( S )-(-)-2-azido-6-(boc-amino)hexanoïque, N3-L-Lys(Boc)-OH
Documents
$35.00 /100 mg
Taille
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Informations sur le produit

Na-Azido-Ne-Boc-L-Lysine is a versatile amino acid derivative that plays a crucial role in bioconjugation and peptide synthesis. This compound features an azido group, which is highly reactive and allows for efficient click chemistry applications, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. The Boc (tert-butyloxycarbonyl) protecting group enhances its stability and facilitates the selective deprotection during synthesis, providing flexibility in various experimental setups.

This compound is particularly valuable in the development of targeted drug delivery systems and the synthesis of complex biomolecules. Its unique properties enable the incorporation of azido groups into peptides, allowing for the creation of novel conjugates that can be used in therapeutic applications, including cancer treatment and vaccine development. Researchers can leverage Na-Azido-Ne-Boc-L-Lysine to explore new avenues in drug design and development, making it a significant addition to any laboratory focused on innovative chemical research.

Numéro CAS 
333366-32-8
Formule moléculaire
C11H20N4O4
Poids moléculaire 
272.3
Point de fusion 
59 - 64 °C
Rotation optique 
[a] D 20 = -42 à -46 º (C=1 dans DMF)
Informations générales
Numéro CAS 
333366-32-8
Formule moléculaire
C11H20N4O4
Poids moléculaire 
272.3
Point de fusion 
59 - 64 °C
Rotation optique 
[a] D 20 = -42 à -46 º (C=1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

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

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to introduce azide groups for further functionalization, which is crucial in drug development.
  • Click Chemistry: Its azido group enables applications in click chemistry, facilitating the rapid and efficient formation of bioconjugates, which are important in creating targeted therapies and diagnostics.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to labels or drugs, enhancing the specificity and efficacy of therapeutic agents in fields like cancer treatment.
  • Protein Engineering: Researchers employ it to modify proteins, improving their stability and activity, which is essential in the development of biopharmaceuticals.
  • Material Science: Its unique properties allow for the creation of functionalized materials, which can be applied in the development of smart materials and sensors.

Citations