Hydrotalcite-like compounds with general formula [M(II)(1-x)M(III)(x)(OH)(2)](x+)(A(x/n)(n-)) mH(2)O, where A(n-) is the compensation anion, were promoted with lanthanum and used as precursors for active catalysts for dry reforming of methane. Four precursors were prepared by co-precipitation and characterized by X-ray diffraction (XRD) and temperature programmed oxidation (TPO-MS). Three of them showed pure hydrotalcite structure. However, Mg/Al molar ratio of 4 provoked the formation of hydromagnesite phase. N-2 physisorption, X-ray diffraction (XRD), temperature programmed reduction (TPR-MS) and X-ray photoelectron spectroscopy (XPS) provided structural, morphological and compositional information about the catalysts. Post-reaction characterization by TPO-MS and scanning electron microscopy (SEM) was also performed in order to evaluate whether carbon actually deposited during reaction. As Mg/Al molar ratio rose, some properties changed: thermal stability increased, BET surface area, and reducibility of Mg(Ni,Al)O decreased while free or segregated NiO reducibility increased. Even though high Mg/Al molar ratios did not favour catalytic activities, it led to enhanced stability during reaction tests, as a consequence of lower deactivation and/or carbon deposition rates. The best stability was achieved at Mg/Al = 3, during a 120 h test. Reduction of Ni inside Ni(Mg,Al)O phase led to a decrease on catalysts' stability. Copyright (c) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.