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Catalog Number:
10621
CAS Number:
103489-33-4
4-(4-Azidophenyl)butyric acid
Purity:
≥ 98% (TLC)
Documents
$58.39 /100MG
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Product Information

4-(4-Azidophenyl)butyric acid is a versatile compound recognized for its unique azide functional group, which enhances its reactivity and applicability in various fields. This compound is particularly valuable in organic synthesis, where it serves as a key intermediate for the development of pharmaceuticals and agrochemicals. Its ability to participate in click chemistry reactions makes it an excellent candidate for bioconjugation applications, allowing researchers to create targeted drug delivery systems and diagnostic tools. Additionally, the compound's structural features enable its use in materials science, particularly in the development of functional polymers and nanomaterials.

The practical applications of 4-(4-Azidophenyl)butyric acid extend to the fields of medicinal chemistry and biotechnology, where it can be utilized in the synthesis of novel compounds with potential therapeutic effects. Its unique properties allow for the modification of biomolecules, enhancing their stability and efficacy. Researchers can leverage this compound to explore new avenues in drug discovery and development, making it a valuable addition to any laboratory focused on innovative chemical research.

CAS Number
103489-33-4
Purity
≥ 98% (TLC)
Molecular Formula
C10H11N3O2
Molecular Weight
205.22
MDL Number
MFCD00798800
PubChem ID
13581615
Appearance
Beige powder
Conditions
Store at RT
General Information
CAS Number
103489-33-4
Purity
≥ 98% (TLC)
Molecular Formula
C10H11N3O2
Molecular Weight
205.22
MDL Number
MFCD00798800
PubChem ID
13581615
Appearance
Beige powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(4-Azidophenyl)butyric 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 targeted delivery in drug development.
  • Photochemistry: It is used in photochemical studies due to its azide functional group, which can undergo photolysis, making it valuable for creating reactive intermediates in synthetic chemistry.
  • Polymer Chemistry: The compound can be incorporated into polymer matrices to enhance properties like thermal stability and mechanical strength, benefiting industries that require durable materials.
  • Medicinal Chemistry: Researchers explore its potential in drug design, particularly in creating prodrugs that can be activated under specific conditions, improving therapeutic efficacy and reducing side effects.
  • Diagnostics: It is utilized in the development of diagnostic tools, where its ability to selectively bind to certain biomolecules can aid in the detection of diseases or pathogens.

Citations