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Catalog Number:
33481
CAS Number:
172531-37-2
Acide 11-azido-3,6,9-trioxaundécanoïque cyclohexylamine
Purity:
99 - 101 % (dosage par titrage)
Synonym(s):
Azido-PEG3-carboxylate, N3-AEEEA·CHA
Documents
$65.40 /100 mg
Taille
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Informations sur le produit

11-Azido-3,6,9-trioxaundecanoic acid cyclohexylamine is a versatile compound known for its unique azido functional group, which enhances its reactivity and potential applications in various fields. This compound is particularly valuable in the synthesis of bioconjugates and drug delivery systems, where its ability to participate in click chemistry reactions allows for the efficient attachment of biomolecules. Researchers in medicinal chemistry and materials science can leverage its properties to develop innovative therapeutic agents and functional materials.

Additionally, the presence of the cyclohexylamine moiety contributes to the compound's solubility and stability, making it suitable for use in aqueous environments. Its unique structure positions it as a promising candidate for applications in polymer chemistry and surface modification, where it can be utilized to create functionalized surfaces with tailored properties. Overall, 11-Azido-3,6,9-trioxaundecanoic acid cyclohexylamine offers significant advantages in the development of advanced materials and biomedical applications, making it an essential addition to any researcher's toolkit.

Numéro CAS 
172531-37-2
Formule moléculaire
C8H15N3O5 · C6H13N
Poids moléculaire 
332.4
Informations générales
Numéro CAS 
172531-37-2
Formule moléculaire
C8H15N3O5 · C6H13N
Poids moléculaire 
332.4
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

11-Azido-3,6,9-trioxaundecanoic acid cyclohexylamine is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Click Chemistry: Its azide functional group makes it an excellent candidate for click chemistry reactions, facilitating the rapid and efficient formation of stable covalent bonds. This is particularly useful in creating complex molecular architectures in pharmaceutical research.
  • Polymer Chemistry: The compound can be incorporated into polymer chains to create functional materials with specific properties, such as increased biocompatibility or improved mechanical strength, which are essential in the development of medical devices.
  • Diagnostic Applications: By enabling the attachment of diagnostic agents to biological targets, this chemical plays a crucial role in the design of biosensors and imaging agents, improving the sensitivity and specificity of medical diagnostics.
  • Drug Development: Its unique structure allows for modifications that can enhance the solubility and bioavailability of pharmaceutical compounds, addressing common challenges in drug formulation and development.

Citations