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Catalog Number:
35151
CAS Number:
80667-36-3
Ácido azido mirístico
Purity:
≥ 95%
Documents
$239.60 /5 mg
Tamaño
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Información del producto

Azido myristic acid is a versatile compound recognized for its unique azide functional group, which enhances its reactivity and applicability in various chemical processes. This fatty acid derivative is particularly valuable in the synthesis of bioactive molecules and can serve as a precursor in the development of pharmaceuticals and agrochemicals. Its ability to participate in click chemistry reactions makes it an attractive option for researchers looking to create complex molecular architectures efficiently.

In addition to its synthetic applications, azido myristic acid is also utilized in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other compounds, which is essential in drug delivery systems and diagnostic tools. Its unique properties enable it to function effectively in lipid modification, providing opportunities for the development of novel materials with tailored functionalities. Researchers and industry professionals can leverage the benefits of azido myristic acid to enhance their projects, making it a valuable addition to any chemical toolkit.

Número CAS
80667-36-3
Fórmula molecular
C12H23N3O2
Peso molecular
241.33
Condiciones
Conservar a -10 °C, desecar y enviar a temperatura ambiente.
Información general
Número CAS
80667-36-3
Fórmula molecular
C12H23N3O2
Peso molecular
241.33
Condiciones
Conservar a -10 °C, desecar y enviar a temperatura ambiente.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Azido myristic acid is widely utilized in research focused on various innovative applications:

  • Bioconjugation: This compound serves as a versatile tool for attaching biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Click Chemistry: Its azide functional group makes it ideal for click chemistry reactions, allowing for the rapid and efficient formation of stable compounds, which is beneficial in creating complex molecular architectures.
  • Antimicrobial Agents: Researchers are exploring its potential as a precursor for synthesizing antimicrobial agents, which can be crucial in developing new treatments for resistant bacterial strains.
  • Polymer Chemistry: Azido myristic acid can be incorporated into polymer matrices, leading to materials with unique properties for applications in coatings, adhesives, and biomedical devices.
  • Fluorescent Probes: It can be modified to create fluorescent probes for imaging applications in biological research, helping scientists visualize cellular processes with greater clarity.

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