112668-54-9
Chemical Structure
16-Azidohexadecanoic acid
- CAS No.: 112668-54-9
- Formula:C16H31N3O2
- Molecular Weight:297.44
IUPAC Name: 16-azidohexadecanoic acid
InChIKey: VLFHDUVVGCRNIZ-UHFFFAOYSA-N
SMILES: O=C(O)CCCCCCCCCCCCCCCN=[N+]=[N-]
Biological Activity: 16-Azidohexadecanoic acid, a synthetic fatty acid, can be used as a modification marker for nucleotides and a molecular probe for fatty acid metabolism[1][2]. 16-Azidohexadecanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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16-Azidohexadecanoic acid | 98.0% | 16-Azidohexadecanoic acid, a synthetic fatty acid, can be used as a modification marker for nucleotides and a molecular probe for fatty acid metabolism. 16-Azidohexadecanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | ||||||||||||||||||||
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- [1]. J Balintová, et al. Antibody-nucleotide conjugate as a substrate for DNA polymerases. Chem Sci. 2018 Jul 24;9(35):7122-7125. [Content Brief]
- [2]. Alexander J Pérez, et al. ω-Azido fatty acids as probes to detect fatty acid biosynthesis, degradation, and modification. J Lipid Res. 2014 Sep;55(9):1897-901. [Content Brief]
Keywords
