Nickel benzoate trihydrate (1) was prepared in singlecrystalline form by the reaction of nickel carbonate with benzoic acid in boiling aqueous solution. Its crystal structure comprises positively charged [Ni(Bz)(H2O)2]n n+ chains, benzoate anions and one independent water molecule of solvation. The hexacoordinated Ni(II) centres in the chains are triply bridged by one syn-syn carboxylato and two aqua bridges. Adjacent chains are linked by O-H•••O hydrogen bonds [O•••O distances in the range 2.647(3) -2.684 (3) Å] through solvate water molecules and benzoate anions. Thermal analysis revealed that 1 is stable up to 100 °C; further heating leads to full dehydration accompanied by an additional decomposition reaction, as characterized by IR spectra of the intermediates. Geometrical features about the Ni centers are compared to similar features at the active sites of urease. The effective magnetic moment per formula unit µeff has a value of 3.17 µB at room temperature and upon cooling reaches a maximum value of 12.39 µB at T = 4.6 K, indicating ferromagnetic coupling between the nearest Ni(II) atoms [3.0671(1) Å] within the chains; at lower temperature this is counteracted by zero-field splitting.