18-Azido-stearic acid serves as a versatile click chemistry reagent characterized by its azide functional group. It acts as a hydrophobic bioconjugation linker and can be modified at the azido-position via copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it is suitable for ring strain-promoted alkyne-azide cycloaddition (SPAAC) when reacted with DBCO or BCN derivatives. This compound is particularly useful in the fields of bioconjugation and chemical biology for the development of complex biomolecular assemblies.
18-Azido-stearic acid serves as a versatile click chemistry reagent characterized by its azide functional group. It acts as a hydrophobic bioconjugation linker and can be modified at the azido-position via copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it is suitable for ring strain-promoted alkyne-azide cycloaddition (SPAAC) when reacted with DBCO or BCN derivatives. This compound is particularly useful in the fields of bioconjugation and chemical biology for the development of complex biomolecular assemblies.
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