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Catalog Number:
23140
CAS Number:
6427-66-3
4-Azidobenzoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
p-Azidobenzoic acid
Hazmat
Documents
$134.70 /1G
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Product Information

4-Azidobenzoic acid is a versatile compound widely recognized for its applications in organic synthesis and materials science. This aromatic azide features a carboxylic acid functional group, making it an excellent candidate for various chemical reactions, including coupling reactions and as a precursor for the synthesis of more complex molecules. Its unique azide functional group allows for click chemistry applications, which are invaluable in bioconjugation and drug development. Researchers utilize 4-Azidobenzoic acid to create functionalized polymers and nanomaterials, enhancing the properties of materials for electronics and biomedical applications.

In addition to its synthetic utility, 4-Azidobenzoic acid serves as a valuable tool in the development of photoresponsive materials and sensors. Its ability to undergo thermal decomposition into nitrogen gas makes it an effective blowing agent in polymer processing. With its diverse range of applications, 4-Azidobenzoic acid stands out as a crucial compound for researchers and industry professionals seeking innovative solutions in chemistry and materials science.

Synonyms
p-Azidobenzoic acid
CAS Number
6427-66-3
Purity
≥ 98% (HPLC)
Molecular Formula
C7H5N3O2
Molecular Weight
163.14
MDL Number
MFCD00013987
PubChem ID
3034184
Appearance
Light yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
p-Azidobenzoic acid
CAS Number
6427-66-3
Purity
≥ 98% (HPLC)
Molecular Formula
C7H5N3O2
Molecular Weight
163.14
MDL Number
MFCD00013987
PubChem ID
3034184
Appearance
Light yellow powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Azidobenzoic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the synthesis of various azide-containing compounds, which are crucial for creating complex molecules.
  • Click Chemistry: Its azide functional group makes it ideal for click chemistry applications, allowing for efficient and selective reactions with alkynes, which are valuable in drug development and materials science.
  • Bioconjugation: In biochemistry, it is used to label biomolecules, enabling the study of protein interactions and cellular processes, which is essential for developing new therapeutic strategies.
  • Polymer Chemistry: The compound can be incorporated into polymer matrices to create materials with specific properties, such as enhanced reactivity or functionality, beneficial in the development of smart materials.
  • Photochemistry: It can be utilized in photochemical reactions, where its azide group can undergo transformations upon light exposure, making it useful in creating light-responsive materials.

Citations