Azidoacetic Acid is a versatile click chemistry reagent characterized by its azide group functionality. It serves as a valuable tool for the synthesis of protein-targeting chimeras, such as PROTACs. Azidoacetic Acid can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds, as well as ring strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN moieties, enabling the rapid assembly of bioconjugates and labeled biomolecules for various research applications.
Azidoacetic Acid is a versatile click chemistry reagent characterized by its azide group functionality. It serves as a valuable tool for the synthesis of protein-targeting chimeras, such as PROTACs. Azidoacetic Acid can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds, as well as ring strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN moieties, enabling the rapid assembly of bioconjugates and labeled biomolecules for various research applications.
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