Simultaneous calculation of the dipole moment μ_j and the relaxation time τ_j of a certain number of non-spherical rigid aliphatic polar liquid molecules (j) in non-polar solvents (i) under 9.8 GHz electric field is possible from real ε′_ij and imaginary ε″_ij parts of the complex relative permittivity ε*_ij. The low frequency and infinite frequency permittivities ε_0ij and ε_∞ij measured by Purohitet al [1,2] and Srivastava and Srivastava [3] at 25, 35 and 30°C respectively are used to obtain static μ_s. The ratio of the individual slopes of imaginary σ″_ij and real σ′_ij parts of high frequency (hf) complex conductivity σ*_ij with weight fractionsw_jatw_j → 0 and the slopes of σ″_ij— σ′_ij curves for differentw_js [4] are employed to obtain τ_js. The former method is better in comparison to the existing one as it eliminates polar-polar interaction. The hf μ_js in Coulomb metre (C m) when compared with static and reported μs indicate that μ_s s favour the monomer formations which combine to form dimers in the hf electric field. The comparison among μs shows that a part of the molecule is rotating under X-band electric field [5]. The theoretical μ_theos from available bond angles and bond moments of the substituent polar groups attached to the parent molecules differ from the measured μ_js and μs to establish the possible existence of mesomeric, inductive and electromeric effects in polar liquid molecules.