The electrochemical behavior of gentisaldehyde (2,5-dihydroxibenzaldehyde) on a glassy carbon electrode is studied by linear-sweep cyclic voltammetry finding one to three oxidation peaks, depending on both the number of cycles recorded and the pH, and one reduction peak. The oxidation product was the formyl-p-benzoquinone, generated by the oxidation of the biphenolic ring, and not the 2,5-dihydroxybenzoic acid (gentisic acid) that could be formed by oxidation of the aldehyde group. The mechanism proposed at pH < pK(1) (8.42) from the analysis of cyclic and convoluted voltammograms involves the loss of an H+ ion from one hydroxyl group, a first quasi-reversible electron transfer to give a radical, and the release of a proton in a third step (the r. d. s.) followed by the second electron transfer to give the product. At pK(1) < pH < pK(2), the electroactive species is the anion that losses an ion H+ to give the dianion, the process being of the CEE type (chemical-electrochemical-electrochemical steps). At pH > pK(2) (10.93) the process becomes of the EE type (electrochemical-electrochemical steps), no H+ ions being involved. Radicals species found justify the antioxidant capacity of gentisaldehyde. (C) 2016 The Electrochemical Society. All rights reserved.