In this study, the physicochemical properties of [NH3(CH2)5NH3]ZnCl4 crystals were investigated using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and nuclear magnetic resonance (NMR). The crystals had a monoclinic structure with C2/c space group and lattice constants are a=21.4175 Å, b=7.3574 Å, c=19.1079 Å, β=120.5190°, and Z=8. Phase-transition temperatures in the DSC curve were 256 K, 390 K, and 481 K. Additionally, a small change near 340 K, related to phase transition, was observed in the XRD pattern. NMR studies indicated no change in 1H chemical shifts, but a change in the chemical shifts for C2, located between C1 and C3 of the cation at 340 K. Increase in molecular motion caused an increase in the spin-lattice relaxation time, T1ρ, at low spinning rates, under magic-angle spinning (MAS) rate conditions. The inorganic anion was composed of octahedral BCl6, when the metal ion (B) was Mn, Cu, and Cd, and tetrahedral BCl4, when B was Zn and Co. The coordination geometries of BCl6 and BCl4, connected by N−H∙∙∙Cl hydrogen bonds between Cl and the organic cation, were investigated.