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Catalog Number:
35109
CAS Number:
824426-32-6
Éster NHS del ácido azidoacético
Purity:
≥ 95% (RMN)
Documents
$214.00 /100 mg
Tamaño
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Información del producto

Azidoacetic acid NHS ester is a versatile compound widely utilized in bioconjugation and peptide synthesis. This NHS (N-hydroxysuccinimide) ester form enhances the reactivity of azidoacetic acid, making it an excellent choice for labeling biomolecules, including proteins and nucleic acids. Its unique azide functional group allows for efficient click chemistry reactions, facilitating the formation of stable conjugates that are crucial in drug development and diagnostic applications. Researchers appreciate its ability to create covalent bonds under mild conditions, which preserves the integrity of sensitive biomolecules.

In addition to its applications in bioconjugation, Azidoacetic acid NHS ester is also employed in the synthesis of various azide-containing compounds, which are valuable in materials science and organic synthesis. Its ease of use and compatibility with a range of substrates make it a preferred choice for chemists looking to explore innovative pathways in their research. With its robust performance and broad applicability, this compound stands out as a key reagent for advancing scientific discovery and development.

Número CAS
824426-32-6
Fórmula molecular
C6H6N4O4
Peso molecular
198.14
Número MDL
MFCD24452499
Condiciones
Conservar a -10 °C, desecar y enviar a temperatura ambiente.
Información general
Número CAS
824426-32-6
Fórmula molecular
C6H6N4O4
Peso molecular
198.14
Número MDL
MFCD24452499
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
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Aplicaciones

Azidoacetic acid NHS ester 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 drug delivery systems and diagnostics.
  • Labeling Techniques: It serves as a reactive probe in labeling experiments, allowing researchers to track biological molecules in live cells, which is crucial for understanding cellular processes.
  • Peptide Synthesis: The compound is used in the synthesis of peptides, facilitating the development of new therapeutic agents in pharmaceuticals, particularly in cancer treatment.
  • Click Chemistry: Its azide functional group enables efficient 'click' reactions, which are valuable in creating complex molecular structures quickly and reliably in materials science.
  • Biomedical Research: This ester is utilized in the development of novel imaging agents and drug candidates, providing a pathway for innovative treatments and diagnostic tools.

Citas