A differential pulse voltammetric method was developed for the sensitive and selective determination of Cu(Ⅱ) at 4-methoxy-2,6-bis(3,5-dimethylpyrazoyl)-l,3,5-triazine modified carbon paste electrode in 0.05 mol/L KHC8H4O4 solution (pH = 4.02). The oxidation peak of Cu(Ⅱ) was observed at 0.065 V(vs Ag/AgCl) by scanning the potential in positive direc-tion. The analysis procedure consisted of an open circuit accumulation step in stirred sample solution. It was followed by medium exchange to a clean solution and subsequently an anodic potential scan was affected to obtain the voltammetric peak. The current was proportional to the concentration of the Cu(Ⅱ) ion in a range of 1× 10-7-1×10-4 mol/L for 6 min accumulation; the most of metal ions did not interfere with the determination. The developed method was applied to Cu(Ⅱ) determination in coal-ash sample, the results agreed with that of atomic adsorption spectroscopy(AAS). A differential pulse voltammetric method was developed for the sensitive and selective determination of Cu (II) at 4-methoxy-2,6-bis (3,5-dimethylpyrazoyl) -l, 3,5-triazine modified carbon paste electrode in 0.05 mol / L KHC8H4O4 solution (pH = 4.02). The analysis peak consisted of an open circuit accumulation step in The was was followed by medium exchange to a clean solution and subsequently an anodic potential scan was affected to obtain the voltammetric peak. The current was proportional to the concentration of the Cu (II) ion in a range of 1 × 10- 7-1 × 10-4 mol / L for 6 min accumulation; the most of metal ions did not interfere with the determination. The developed method was applied to Cu (Ⅱ) determination in coal-ash sample, the results agreed with that of atomic adsorption spectroscopy (AAS).