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Catalog Number:
06162
CAS Number:
33173-53-4
4-Azido-L-phenylalanine
Purity:
≥ 99.9% (Chiral HPLC)
Synonym(s):
L-Phe(4-azido)-OH, p-Azido-L-phenylalanine
Documents
$77.32 /100MG
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Product Information

4-Azido-L-phenylalanine is a versatile amino acid derivative that has gained significant attention in the fields of biochemistry and molecular biology. This compound, characterized by its unique azido group, serves as a powerful tool for bioconjugation and labeling applications. Researchers utilize 4-Azido-L-phenylalanine to incorporate azide functionalities into proteins and peptides, facilitating the study of protein interactions and dynamics. Its ability to undergo click chemistry reactions makes it particularly valuable for creating complex biomolecular structures, enhancing the understanding of cellular processes.

In addition to its applications in protein engineering, 4-Azido-L-phenylalanine is also explored in drug development and delivery systems. The azido group allows for selective modification of therapeutic agents, potentially improving their efficacy and targeting capabilities. With its unique properties and diverse applications, 4-Azido-L-phenylalanine stands out as an essential compound for researchers aiming to innovate in the fields of biotechnology and pharmaceuticals.

Synonyms
L-Phe(4-azido)-OH, p-Azido-L-phenylalanine
CAS Number
33173-53-4
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C9H10N4O2
Molecular Weight
206.1
MDL Number
MFCD00238100
PubChem ID
14443196
Appearance
Off-white crystalline or brownish powder
Conditions
Store at ≤ -20 °C
General Information
Synonyms
L-Phe(4-azido)-OH, p-Azido-L-phenylalanine
CAS Number
33173-53-4
Purity
≥ 99.9% (Chiral HPLC)
Molecular Formula
C9H10N4O2
Molecular Weight
206.1
MDL Number
MFCD00238100
PubChem ID
14443196
Appearance
Off-white crystalline or brownish powder
Conditions
Store at ≤ -20 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Bioconjugation: This compound is often used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Protein Labeling: Researchers employ 4-Azido-L-phenylalanine for the site-specific labeling of proteins, allowing for better tracking and analysis of protein interactions in cellular studies.
  • Photochemistry: Its azido group can undergo photochemical reactions, making it valuable in creating light-responsive materials and in studies involving photo-crosslinking.
  • Drug Development: The compound is explored in the synthesis of novel pharmaceuticals, particularly in creating compounds that can selectively target specific cells or tissues.
  • Research in Neuroscience: It is used in studies related to neurotransmitter pathways, helping to understand the role of amino acids in brain function and potential therapeutic targets.

Citations