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Catalog Number:
35116
CAS Number:
1306615-47-3, 1951424-99-9
Azoture de desthiobiotine
Purity:
≥ 95 % (RMN)
Documents
$86.23 /5 mg
Taille
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Informations sur le produit

Desthiobiotin azide is a versatile chemical compound that serves as a valuable tool in bioconjugation and labeling applications. This compound is particularly notable for its azide functional group, which allows for efficient click chemistry reactions, enabling researchers to attach various biomolecules, such as proteins or nucleic acids, to surfaces or other molecules. Its unique structure, featuring a hexanamide backbone and a biotin moiety, enhances its affinity for streptavidin, making it an excellent choice for applications in proteomics and diagnostics.

In the field of drug development and molecular biology, Desthiobiotin azide can be utilized for the synthesis of bioconjugates, facilitating the study of protein interactions and cellular processes. Its ability to form stable conjugates with a wide range of biomolecules opens up possibilities for targeted drug delivery systems and the development of novel therapeutic agents. Researchers will find this compound particularly beneficial for enhancing the specificity and efficacy of their experiments, ultimately leading to more accurate results and advancements in their respective fields.

Numéro CAS 
1306615-47-3, 1951424-99-9
Formule moléculaire
C18H34N6O5
Poids moléculaire 
414.5
Informations générales
Numéro CAS 
1306615-47-3, 1951424-99-9
Formule moléculaire
C18H34N6O5
Poids moléculaire 
414.5
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

Desthiobiotin azide is widely utilized in research focused on:

  • Bioconjugation: This compound is essential for attaching biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted therapies and diagnostics.
  • Labeling and Imaging: Its azide functional group allows for click chemistry applications, making it useful in labeling biomolecules for imaging studies in cellular biology, aiding researchers in tracking molecular interactions.
  • Drug Development: In pharmaceutical research, it serves as a tool for synthesizing new drug candidates, particularly in the creation of biotinylated compounds that can improve drug delivery systems.
  • Protein Purification: The compound can be used in affinity chromatography, where it helps in the purification of proteins by binding to biotinylated targets, streamlining the process for researchers.
  • Diagnostics: Its applications extend to the development of diagnostic assays, where it can be integrated into tests for various diseases, providing a reliable method for detecting specific biomolecules.

Citations