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Catalog Number:
35109
CAS Number:
824426-32-6
Azidoacetic acid NHS ester
Purity:
≥ 95% (NMR)
Documents
$214.00 /100MG
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Product Information

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.

CAS Number
824426-32-6
Purity
≥ 95% (NMR)
Molecular Formula
C6H6N4O4
Molecular Weight
198.14
MDL Number
MFCD24452499
PubChem ID
59248176
Appearance
White to off-white solid
Conditions
Store at -10 °C, desiccate and shipped at ambient temperature
General Information
CAS Number
824426-32-6
Purity
≥ 95% (NMR)
Molecular Formula
C6H6N4O4
Molecular Weight
198.14
MDL Number
MFCD24452499
PubChem ID
59248176
Appearance
White to off-white solid
Conditions
Store at -10 °C, desiccate and shipped at ambient temperature
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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.

Citations