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Catalog Number:
33467
CAS Number:
166388-57-4
Tosylate de 1-Amino-8-azido-3,6-dioxaoctane
Purity:
99 - 101 % (dosage par titrage)
Synonym(s):
H2N-PEG(2)-N3·TosOH, Azido-PEG2-amine tosylate
Antibiotic
Documents
$60.40 /100 mg
Taille
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Informations sur le produit

1-Amino-8-azido-3,6-dioxaoctane tosylate is a versatile compound that plays a significant role in various fields, particularly in chemical synthesis and pharmaceutical research. This compound, with its unique azido group, is particularly valuable for click chemistry applications, allowing for the efficient formation of covalent bonds in the development of new materials and drug candidates. Its dioxaoctane backbone enhances solubility and stability, making it an excellent choice for researchers looking to create complex molecular architectures.

In addition to its utility in synthetic chemistry, 1-Amino-8-azido-3,6-dioxaoctane tosylate can be employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules. This capability is crucial in the development of targeted drug delivery systems and diagnostic tools. The compound's favorable properties, such as its ease of handling and compatibility with various reaction conditions, make it an attractive option for both academic and industrial applications.

Numéro CAS 
166388-57-4
Formule moléculaire
C6H14N4O2 · C7H8O3S
Poids moléculaire 
346.4
Point de fusion 
53 - 63 °C
Informations générales
Numéro CAS 
166388-57-4
Formule moléculaire
C6H14N4O2 · C7H8O3S
Poids moléculaire 
346.4
Point de fusion 
53 - 63 °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

1-Amino-8-azido-3,6-dioxaoctane tosylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing novel pharmaceuticals, particularly in the development of azide-containing drugs, which can enhance therapeutic efficacy.
  • Bioconjugation Techniques: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating targeted drug delivery systems.
  • Material Science: The compound is used in the creation of functionalized polymers, which can improve the properties of materials used in coatings, adhesives, and other industrial applications.
  • Click Chemistry: This chemical plays a significant role in click chemistry reactions, enabling the rapid and efficient formation of complex molecular structures, which is crucial in various fields including drug discovery.
  • Diagnostic Applications: It is also utilized in developing diagnostic agents, particularly in imaging techniques where azide functionalities can enhance the visibility of biological markers.

Citations