Abstract A series of twelve 2, 5-bis (alkylamino)-1, 4-benzoquinones were prepared in yields ranging from 9–58% via the reaction between p-benzoquinone and various amines. The structures of the synthesized compounds were confirmed by IR, 1 H-and 13 C-NMR and MS analyses. The phytotoxicity of the 2, 5-bis (alkylamino)-1, 4-benzoquinones was evaluated against two crop species, Cucumis sativus and Sorgum bicolor, at 1.0× 10-3 mol/L. In ...