The densities and viscosities of Glycine in five aqueous solutions of Sodium Sulphate, were measured in the temperature range from 283.15 to 308.15 K at intervals of 5 K, using a vibrating U-tube densimeter Anton Paar DMA 5000 and the Automatic Microviscosimeter AMVn, respectively. The measured densities were used to calculate the limit-apparent molar volume (V-phi(0)), limit-transfer molar volume (Delta V-tr(phi)0)and hydration number (n(h)). The partial volumes at infinite dilution of the glycine in aqueous solution of sodium sulfate were evaluated through extrapolation at each temperature. The behavior of Delta V-tr(phi)0 was interpreted in terms of solute-solvent interactions on the basis of the cosphere-overlap model. The hydration numbers were positive and interpreted in terms of dehydration and electrostriction effects. The relative viscosity data were adjusted by least-squares for obtain the Jones-Dole equation coefficients A, B and D. To accompany the experimental results, a series of small molecular complexes simulating the interactions present in the glycine + water/sodium sulfate systems were modeled by the Density Functional Theory with the basis function 6-31G(d). From viscosity dates, the activation parameters of the viscous flow (free molar energy of Gibbs Delta G(not equal), enthalpy Delta N-not equal, and entropy Delta S-not equal) were evaluated. The temperature dependence of the partial molar volume at infinite dilution and the viscosity B coefficient were discussed in terms of the dominant interactions in solution; it was found that the glycine has a making effect in the structure of the solvent, and at infinite dilution ion-solvent interactions are dominant between NH3+ and COO- groups of the amino acid with Na+ and SO42- ions. From the theoretical point of view, the complexes studied turned out to be stable and represent a good approximation to rationalize the intermolecular interactions that occur in glycine + water/sodium sulphate mixtures. (C) 2018 Published by Elsevier B.V.