We demonstrate that non-equilibrium nuclear spin order survives precipitation from solution and redissolution. The effect is demonstrated on 13 C-and 2 H-labeled sodium fumarate, with precipitation and dissolution achieved by altering the pH. The lifetimeo ft he spin magnetization in the precipitate suspension is found to be much longert han in solution. Our preliminary results showa nextension of the effective relaxation time T 1 for the metabolite fumarate by af actor of % 6. We show that when the free radical agent TEMPO is present in the solution, it is not incorporatedi nto the precipitate, suggesting that this procedure mayp rovide am eans to store and transport agents polarized by dynamic nuclear polarization. Although the relaxation time, T 1 ,o ft he precipitate suspensioni sl onger than that of the same molecules in solution, it is significantly shorter than that observed in the immobilizeds olid state.Nuclearm agnetic resonance (NMR) provides valuable chemical, structural,a nd dynamical information, but suffers from low signal strength.H yperpolarization can be used to enhancet he nuclear spin order in molecules by factors of % 10 5 compared to highfield thermalequilibrium magnetization, to give greatly enhanced signals. [1][2][3][4][5][6][7][8][9][10] Clinical studies involving hyperpolarized [1-13 C]pyruvate have been used to monitor tumour metabolism. [2] In vivo imaging studies have also been performed using hyperpolarized [1-13 C]fumarate. [3] Hyperpolarization methods are limited by an intrinsic longitudinalr elaxation time (T 1 )t hat governst he return of nonequilibriumm agnetization to thermal equilibrium.T he time for extractingt he sample from the hyperpolarizatione quipment, purification, transport, delivery,a nd signal acquisition is often similar to the nuclear T 1 ,m eaning that the polarizer needs to be located close to the point of use.Efforts have been made towards the goal of storing hyperpolarizedm agnetization in the solid state. [11,12] This is difficult in the case of dynamic nuclear polarization( DNP) where radicals are used for the polarization step, because they can induce rapid nuclear spin relaxation, especiallyi nt he solid state. [13] Onea pproach employs heterogeneousm aterials, in which the hyperpolarized spin order is transportedb ys pin diffusion to regions distant from the unpaired electron sites. [4] Another approach is to induce radical formation at low temperature by ultraviolet irradiation. The UV-induced radicals are quenched when the sample is warmed. [5] It is also possible to immobilize the radicals by attachment to am atrix, so that they remain behind when the polarizedm ateriali sf lushedo ut. [9,10] In this paper we demonstrate the possibility of ad ifferent procedure, in which ap olarized solution is prepared and the sample precipitated to form as uspension of microcrystals. We show that non-equilibrium magnetization is substantially preservedi nt his process,a llowing the polarized substance to be liberated into solution by redissolving the solid at al a...