For other salt forms please inquire. The azide-containing 7-N₃Ac-AParg-7-C-dATP is an analogue of dATP and a suitable molecular tool for the copper(I)-catalysed Huisgen azide-alkyne [3+2] cycloaddition (CuAAC) or copper(I)-free strain-promoted Alkyne-Azide Click Chemistry (SPAAC) with strained alkynes, respectively. Both reactions have attracted particular interest for the introduction of reporter groups and for the labelling of various biomolecules like dATP-binding proteins by the so-called click-chemistry technique. Azide-functionalised 7-deaza purine nucleotides can replace their natural counterpart dATP in polymerase reactions, resulting in functionalized DNA that can subsequently be further reacted and modified using click chemistry methods. References for CuAAC and SPAAC click chemistry: Dommerholt et al., Top. Curr. Chem., 374:16 (2016); Presolski et al., Curr. Protoc. Chem. Biol., 3, 153 - 162 (2011); Hong et al., Angew. Chem. Int. Ed. Engl., 48, 9879 - 9883 (2009)

Vial containing 250 µl of 1 mM aqueous solution of pH 7.6