The voltammetric behavior of synthetic food antioxidants, such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), propyl gallate (PG) and tert-butylhydroquinone (TBHQ), at a glassy carbon electrode in solution of 0.1 mol l(-1) perchloric acid containing 1% methanol has been investigated. The obtained linear sweep voltammograms (LSV) showed that all these four compounds have well-defined oxidation waves with peak potentials of 629, 818, 599 and 501 mV for BHA, BHT, PG and TBHQ, respectively. Linear calibration graphs were also obtained in the concentration ranges of 0.5-15.0, 0.5-8.0, 1.0-15.0 and 1.0-15.0 mg l(-1) for BHA, BHT, PG and TBHQ, respectively However, the voltammetric peaks of these antioxidants seriously overlap and it is difficult to determine them individually from a mixture without prior separation. In this work, a method for simultaneous determination of these antioxidants, based on their oxidation at the grassy carbon electrode, with the aid of chemometric approaches, such as classical least squares (CLS), principal component regression (PCR) and partial least squares (PLS), has been developed. The method was applied to determine the four antioxidants in a set of synthetic mixtures and several commercial food samples; in general, satisfactory results were obtained. (C) 2000 Elsevier Science B.V. All rights reserved.