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Catalog Number:
33505
CAS Number:
2250433-81-7
Fmoc-N-(4-azidobutyl)glycine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-Abg(N3)-OH
Antibiotic
Documents
$161.64 /100MG
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Product Information

Fmoc-N-(4-azidobutyl)glycine is a versatile building block in peptide synthesis, particularly valued for its unique azide functional group, which enables click chemistry applications. This compound is widely utilized in the development of bioconjugates and drug delivery systems, where its ability to form stable linkages with various biomolecules enhances the efficacy of therapeutic agents. The Fmoc protecting group allows for easy incorporation into peptide chains, making it an ideal choice for researchers focused on synthesizing complex peptides with specific functionalities.

In addition to its role in peptide synthesis, Fmoc-N-(4-azidobutyl)glycine is also instrumental in the development of novel materials and surface modifications. Its azide moiety can participate in a variety of reactions, including the well-known Huisgen cycloaddition, facilitating the creation of diverse polymeric structures. This compound's unique properties and functional versatility make it an essential tool for researchers in medicinal chemistry, materials science, and biochemistry, driving innovation in drug design and delivery.

Synonyms
Fmoc-Abg(N3)-OH
CAS Number
2250433-81-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H22N4O4
Molecular Weight
394.4
PubChem ID
127239814
Melting Point
89 - 92 °C
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-Abg(N3)-OH
CAS Number
2250433-81-7
Purity
≥ 99% (HPLC)
Molecular Formula
C21H22N4O4
Molecular Weight
394.4
PubChem ID
127239814
Melting Point
89 - 92 °C
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

Fmoc-N-(4-azidobutyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, allowing for the incorporation of azide groups that facilitate further chemical modifications.
  • Bioconjugation: Its azide functionality is crucial for click chemistry applications, enabling researchers to attach biomolecules, such as proteins or nucleic acids, to surfaces or other molecules efficiently.
  • Drug Development: The compound can be used in the design of novel therapeutics, particularly in creating targeted drug delivery systems that enhance the efficacy of treatments.
  • Material Science: It is applied in the development of functionalized materials, where the azide group can be used to create polymers with specific properties for various industrial applications.
  • Diagnostics: The compound can be utilized in the development of diagnostic tools, where its unique properties allow for the detection of specific biomolecules in biological samples.

Citations