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Catalog Number:
47697
CAS Number:
159610-92-1
6-Azido-L-lysine
Purity:
≥ 99% (HPLC)
Synonym(s):
H-Lys(N3)-OH, 6-Azido-L-norleucine
Documents
$65.00 /25MG
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Product Information

6-Azido-L-lysine is a versatile amino acid derivative that plays a crucial role in various biochemical applications, particularly in the fields of bioconjugation and drug development. This compound is recognized for its unique azido functional group, which allows for selective reactions in click chemistry, making it an invaluable tool for researchers looking to create complex biomolecules. Its ability to participate in bioorthogonal reactions enables the labeling and tracking of proteins and other biomolecules in live cells, facilitating advancements in cellular imaging and targeted therapy.

In addition to its applications in research, 6-Azido-L-lysine is also utilized in the synthesis of peptide-based drugs and in the development of novel therapeutic agents. Its stability and reactivity make it an ideal candidate for incorporation into various drug delivery systems, enhancing the efficacy of therapeutic compounds. Researchers and industry professionals can leverage the unique properties of 6-Azido-L-lysine to innovate in areas such as vaccine development, cancer therapy, and the creation of diagnostic tools, making it a valuable asset in modern biochemical research.

Synonyms
H-Lys(N3)-OH, 6-Azido-L-norleucine
CAS Number
159610-92-1
Purity
≥ 99% (HPLC)
Molecular Formula
C6H12N4O2
Molecular Weight
172.2
Appearance
White powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
H-Lys(N3)-OH, 6-Azido-L-norleucine
CAS Number
159610-92-1
Purity
≥ 99% (HPLC)
Molecular Formula
C6H12N4O2
Molecular Weight
172.2
Appearance
White powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Azido-L-lysine is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile building block for bioconjugation, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing drug delivery systems.
  • Click Chemistry: It plays a crucial role in click chemistry reactions, which are used to create complex molecular structures quickly and efficiently, making it valuable in drug discovery and development.
  • Protein Labeling: The azido group enables specific labeling of proteins in biological studies, aiding in the visualization and tracking of protein interactions within cells.
  • Peptide Synthesis: As a modified amino acid, it is used in peptide synthesis to create novel peptides with unique properties, which can be used in therapeutic applications.
  • Research in Neuroscience: It is being explored for its potential in neuroscience research, particularly in studying neuronal signaling and the development of neuroprotective agents.

Citations