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Catalog Number:
33505
CAS Number:
2250433-81-7
Fmoc-N-(4-azidobutyl)glycine
Purity:
≥ 99 % (HPLC)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
Antibiotic
Documents
$161.64 /100 mg
Taille
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Informations sur le produit

Fmoc-N-(4-azidobutyl)glycine is a versatile building block in peptide synthesis, particularly valued for its unique azide functional group, which enables click chemistry applications. This compound is widely utilized in the development of bioconjugates and drug delivery systems, where its ability to form stable linkages with various biomolecules enhances the efficacy of therapeutic agents. The Fmoc protecting group allows for easy incorporation into peptide chains, making it an ideal choice for researchers focused on synthesizing complex peptides with specific functionalities.

In addition to its role in peptide synthesis, Fmoc-N-(4-azidobutyl)glycine is also instrumental in the development of novel materials and surface modifications. Its azide moiety can participate in a variety of reactions, including the well-known Huisgen cycloaddition, facilitating the creation of diverse polymeric structures. This compound's unique properties and functional versatility make it an essential tool for researchers in medicinal chemistry, materials science, and biochemistry, driving innovation in drug design and delivery.

Numéro CAS 
2250433-81-7
Formule moléculaire
C21H22N4O4
Poids moléculaire 
394.4
Point de fusion 
89 - 92 °C
Informations générales
Numéro CAS 
2250433-81-7
Formule moléculaire
C21H22N4O4
Poids moléculaire 
394.4
Point de fusion 
89 - 92 °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

Fmoc-N-(4-azidobutyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, allowing for the incorporation of azide groups that facilitate further chemical modifications.
  • Bioconjugation: Its azide functionality is crucial for click chemistry applications, enabling researchers to attach biomolecules, such as proteins or nucleic acids, to surfaces or other molecules efficiently.
  • Drug Development: The compound can be used in the design of novel therapeutics, particularly in creating targeted drug delivery systems that enhance the efficacy of treatments.
  • Material Science: It is applied in the development of functionalized materials, where the azide group can be used to create polymers with specific properties for various industrial applications.
  • Diagnostics: The compound can be utilized in the development of diagnostic tools, where its unique properties allow for the detection of specific biomolecules in biological samples.

Citations