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Catalog Number:
29577
CAS Number:
1257063-35-6
15-Azido-4,7,10,13-tetraoxapentadecanoic acid
Purity:
≥ 97% (NMR)
Synonym(s):
N3-(PEG)4-COOH, Azido-(PEG)4-acid
Documents
$127.79 /25MG
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Product Information

15-Azido-4,7,10,13-tetraoxapentadecanoic acid is a versatile compound that has garnered attention in various fields, particularly in bioconjugation and drug delivery systems. This unique azido fatty acid derivative is characterized by its multiple ether linkages, which enhance its solubility and reactivity, making it an excellent candidate for applications in medicinal chemistry and materials science. Researchers can leverage its azide functional group for click chemistry, facilitating the attachment of biomolecules or drug moieties to surfaces or polymers, thereby improving the efficacy of therapeutic agents.

The compound's structure allows for easy modification and functionalization, which is crucial in the development of targeted drug delivery systems. Its potential applications extend to the synthesis of biocompatible materials and the creation of advanced nanocarriers for pharmaceuticals. With its unique properties, 15-Azido-4,7,10,13-tetraoxapentadecanoic acid stands out as a valuable tool for researchers aiming to innovate in drug formulation and delivery technologies.

Synonyms
N3-(PEG)4-COOH, Azido-(PEG)4-acid
CAS Number
1257063-35-6
Purity
≥ 97% (NMR)
Molecular Formula
C11H21N3O6
Molecular Weight
291.3
MDL Number
MFCD12406155
PubChem ID
22731907
Appearance
Light yellow to colorless thick liquid
Conditions
Store at 0-8 °C
General Information
Synonyms
N3-(PEG)4-COOH, Azido-(PEG)4-acid
CAS Number
1257063-35-6
Purity
≥ 97% (NMR)
Molecular Formula
C11H21N3O6
Molecular Weight
291.3
MDL Number
MFCD12406155
PubChem ID
22731907
Appearance
Light yellow to colorless thick liquid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

15-Azido-4,7,10,13-tetraoxapentadecanoic acid is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules, such as proteins or antibodies, to surfaces or other molecules for enhanced functionality in drug delivery systems.
  • Click Chemistry: Its azide functional group makes it ideal for click chemistry applications, facilitating the rapid and selective formation of covalent bonds, which is crucial in developing new materials and pharmaceuticals.
  • Nanotechnology: In the field of nanotechnology, it is used to modify nanoparticles for targeted drug delivery, improving the efficacy and reducing side effects of therapeutic agents.
  • Biomedical Research: The compound plays a significant role in the development of imaging agents and contrast materials, enhancing the visualization of biological processes in medical diagnostics.
  • Polymer Chemistry: It is employed in synthesizing functionalized polymers, which can be tailored for specific applications in coatings, adhesives, and biomedical devices, providing unique properties compared to traditional materials.

Citations