Pullulan derivative was synthesized by coupling carboxymethylpullulan (degree of substitution DS0in = 0.7) and dimethylaminopropylamine (DMAPA), activated by a hydrosoluble carbodiimide N'-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (EDAC). FTIR and C-13 and H-1 NMR spectroscopic analyses have evidenced that the polysaccharide has been successfully modified. 1 H NMR, nitrogen analysis, and conductimetric measurements allow determination of the degree of substitution in both carboxylic acid and amine functions. We have found that both functions present a similar DS of 0.35, which is characteristic of an ampholytic polymer with possible zwitterionic-type properties. Solution properties have been studied by flow field flow fractionation (F4) coupled on-line with multiangle laser light scattering (MALLS) and quasi elastic light scattering (QELS), surface tension, and viscosity measurements. The behavior has been found largely pH dependent and an amphiphilic behavior has been evidenced in alkaline media. (c) 2007 Elsevier Inc. All rights reserved.