By using the instantaneous probability density distribution for 1D Fokker-P
lanck equation, the internal-spatially local entropy density and entropy fl
ux for chemically reacting species in solution are defined for the first ti
me without the local equilibrium assumption. The local heat flux is then de
fined via the entropy flux and kinetic temperature. It is proved that such
heat flux should reasonably coincide with that under the local equilibrium
if the local equilibrium probability distribution is utilized. The internal
-spatially local entropy production rate is defined at the same time. These
quantities should offer helpful measures for understanding transient dynam
ics of chemical reactions in solution.