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Catalog Number:
05752
CAS Number:
163217-43-4
Fmoc-4-azido-L-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Phe(4-azido)-OH, Fmoc-p-azido-L-Phe-OH, (S-Fmoc-2-amino-3-(4-azidophenyl)propionic acid
Documents
$120.88 /250MG
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Product Information

Fmoc-4-azido-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique azido group, which allows for efficient click chemistry reactions, making it an excellent choice for researchers looking to develop novel biomaterials or drug delivery systems. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group provides stability during synthesis, ensuring high purity and yield in peptide formation.

In the pharmaceutical and biotechnology sectors, Fmoc-4-azido-L-phenylalanine is particularly valuable for creating labeled peptides and studying protein interactions. Its ability to facilitate the incorporation of azide functionalities into peptides opens up new avenues for research in targeted therapies and diagnostic applications. With its favorable properties and practical applications, this compound stands out as an essential tool for professionals in the fields of medicinal chemistry and molecular biology.

Synonyms
Fmoc-L-Phe(4-azido)-OH, Fmoc-p-azido-L-Phe-OH, (S-Fmoc-2-amino-3-(4-azidophenyl)propionic acid
CAS Number
163217-43-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20N4O4
Molecular Weight
428.5
MDL Number
MFCD00237665
PubChem ID
20674486
Appearance
Off-white to brownish powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Phe(4-azido)-OH, Fmoc-p-azido-L-Phe-OH, (S-Fmoc-2-amino-3-(4-azidophenyl)propionic acid
CAS Number
163217-43-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20N4O4
Molecular Weight
428.5
MDL Number
MFCD00237665
PubChem ID
20674486
Appearance
Off-white to brownish powder
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

Fmoc-4-azido-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various studies in biochemistry and molecular biology.
  • Click Chemistry: Its azide functional group enables efficient click chemistry reactions, facilitating the attachment of other molecules in drug development and biomolecular research.
  • Fluorescent Labeling: The unique properties of Fmoc-4-azido-L-phenylalanine make it suitable for fluorescent labeling applications, helping scientists track and visualize proteins in live cells.
  • Drug Development: This compound can be used in the design of new pharmaceuticals, particularly in targeting specific proteins or pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: It plays a significant role in bioconjugation processes, allowing for the attachment of therapeutic agents to antibodies or other biomolecules, improving targeted delivery systems.

Citations