Nitrogen-containing volatile organic compounds (NVOCs) can cause great damage to human health and the atmospheric environment. However, the efficient oxidation of nbutylamine at low temperature and effective inhibition of the production of hazardous NH 3 and NO x byproducts remain a great challenge. Herein, hierarchical Cu−Mn composite oxide catalysts with diverse Cu−Mn ratios were rationally prepared, and the intrinsic role of Cu and Mn sites in n-butylamine oxidation was elucidated. As a powerful catalyst, n-butylamine (1000 ppm; GHSV = 60 000 h −1 ) can be completely mineralized over Cu 0.25 Mn 0.75 at 280 °C with greatly enhanced N 2 selectivity (95%) and low yield of nitrogen-containing byproducts (NH 3 , NO, NO 2 , and N 2 O). The superior n-butylamine conversion and mineralization rate of Cu 0.25 Mn 0.75 is owing to its high content of Mn 4+ species and the formation of preferred crystal face for nbutylamine absorption. The proper Cu−Mn ratio of catalyst can inhibit the production of NH 3 in low temperature, and its high pore volume promote the diffusion of NH x species which further suppress NH x oxidation to NO x . Hence, the proper Cu/Mn ratio is conducive to enhancing N 2 selectivity. In situ DRIFTS results show that amides, alcohols, and acids are the main intermediates during n-butylamine combustion. The C−N breakage is the rate-controlling step, and the mineralization rate of intermediates can be remarkably boosted over Cu 0.25 Mn 0.75 due to its high content of Mn 4+ species. This study enriches our understanding of designing efficacious catalysts combining high activity and N 2 selectivity for industrial NVOC purification.