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Catalog Number:
37073
CAS Number:
866363-70-4
Ester N- hydroxysuccinimidylique de l'acide 6-azidocaproïque
Purity:
≥ 99 % (HPLC)
Synonym(s):
N 3 -Aca-OSu
Documents
$181.67 /100 mg
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Product Information

6-Azidocaproic acid N-hydroxysuccinimidyl ester is a versatile compound widely utilized in bioconjugation and labeling applications. This reactive ester is particularly valuable for researchers looking to attach azide groups to biomolecules, facilitating the development of novel bioconjugates for drug delivery, imaging, and diagnostics. Its unique azido functionality allows for click chemistry reactions, enabling efficient and selective conjugation with alkyne-containing partners. This property makes it an essential tool in the fields of biochemistry and molecular biology, where precise modifications of proteins and nucleic acids are crucial.

In addition to its applications in bioconjugation, 6-Azidocaproic acid N-hydroxysuccinimidyl ester can be employed in the synthesis of various functionalized materials, enhancing the performance of biomaterials and drug formulations. Its stability and reactivity under physiological conditions make it an ideal candidate for developing targeted therapies and advanced diagnostic tools. Researchers and industry professionals can leverage this compound to create innovative solutions that meet the growing demands of modern science and healthcare.

Synonyms
N 3 -Aca-OSu
CAS Number
866363-70-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H14N4O4
Molecular Weight
254.2
MDL Number
MFCD25968077
PubChem ID
11594035
Appearance
Huile jaune clair
Conditions
Conserver à - 20 °C
General Information
Synonyms
N 3 -Aca-OSu
CAS Number
866363-70-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H14N4O4
Molecular Weight
254.2
MDL Number
MFCD25968077
PubChem ID
11594035
Appearance
Huile jaune clair
Conditions
Conserver à - 20 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Azidocaproic acid N-hydroxysuccinimidyl ester is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing the functionality of diagnostics and therapeutics.
  • Drug Development: In pharmaceutical research, it is used to create targeted drug delivery systems, improving the efficacy of drugs by ensuring they reach specific cells or tissues, which is crucial in cancer therapy.
  • Protein Labeling: The compound is valuable for labeling proteins with azide groups, facilitating the study of protein interactions and functions through techniques like click chemistry, which is efficient and selective.
  • Material Science: It finds applications in the development of smart materials that respond to environmental stimuli, such as temperature or pH changes, making it useful in creating advanced sensors and actuators.
  • Diagnostics: Its ability to form stable conjugates makes it a key player in the development of diagnostic tools, such as imaging agents for medical imaging techniques, enhancing the detection of diseases.

Citations