The electronic structure and magnetic properties of polycrystalline BaTi1-xMnxO3 (x = 0-0.1) compounds prepared by solid-state reactions were studied. The results revealed that the increase in Mn content (x) did not change the oxidation numbers of Ba (+2) and Ti (+4) in BaTi1-xMnxO3. However, there is the change in Mn valence that Mn-3+,Mn-4+ ions coexist in the samples with x = 0.01-0.04 while Mn4+ ions are almost dominant in the samples with x = 0.06-0.1. We also point out that Mn3+ and Mn4+ ions substitute for Ti4+ and prefer locating in the tetragonal and hexagonal BaTiO3 structures, respectively, in which the hexagonal phase constitutes soon as x = 0.01. Particularly, all the samples exhibit room-temperature ferromagnetism. Ferromagnetic order increases with increasing x from 0 to 0.02, but decreases as x >= 0.04. We think that ferromagnetism in BaTi1-xMnxO3 is related to lattice defects and/or exchange interactions between Mn3+ and Mn4+ ions. (C) 2017 Elsevier B.V. All rights reserved.