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Catalog Number:
33467
CAS Number:
166388-57-4
Tosilato de 1-amino-8-azido-3,6-dioxaoctano
Purity:
99 - 101% (Ensayo por titulación)
Synonym(s):
H2N-PEG(2)-N3·TosOH, Tosilato de azido-PEG2-amina
Antibiotic
Documents
$60.40 /100 mg
Tamaño
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Información del producto

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.

Número CAS
166388-57-4
Fórmula molecular
C6H14N4O2 · C7H8O3S
Peso molecular
346.4
Número MDL
MFCD23380095
Punto de fusión
53 - 63 °C
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
166388-57-4
Fórmula molecular
C6H14N4O2 · C7H8O3S
Peso molecular
346.4
Número MDL
MFCD23380095
Punto de fusión
53 - 63 °C
Condiciones
Conservar entre 2 y 8 °C.
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

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.

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