Sodium tetrachloroaurate is used wherever chloroauric acid would be but the free acid is a nuisance. In nanoparticle synthesis it gives the same citrate-, borohydride- and seed-mediated products with less pH drift, and in the deposition–precipitation preparation of supported gold catalysts (Au/TiO₂, Au/CeO₂, Au/Fe₂O₃) it reduces the amount of base needed to reach the pH 7–9 window at which [AuCl₄]⁻ hydrolyses to the hydroxo species that deposit on the support.
In homogeneous catalysis sodium tetrachloroaurate is a convenient gold(III) source for alkyne hydration, hydroamination and Friedel–Crafts-type additions, and for the oxidative coupling chemistry of gold(III). It is reduced by dimethyl sulfide, thiodiglycol or triphenylphosphine to the gold(I) chlorides used to make phosphine and N-heterocyclic carbene gold catalysts and luminescent gold complexes.
Other uses are electroless and immersion gold plating baths, the gold loading of resins and polymers, gold recovery and refining test work, and medicinal-chemistry research into gold(III) complexes. Its sodium content is irrelevant for most of these and an advantage where a chloride-rich, metal-ion-containing solution is being prepared anyway.