Valerii P. Sazonov Solubility, Solubility data series The analytical method was used. A sample of (2) was placed with the appropriate amount of pure solvent in a small flask. The contents of the flask were warmed to 30 to 50 °C, agitated with excess crystals for 15 min, and then placed in a constant temperature bath at 20 °C with intermittent shaking for 6 to 8 h. Crystallization of the supersaturated solution occurred, and when equilibrium was reached the solution was quickly decanted, filtered from the fine crystals, and placed in a stoppered flask at 20 °C for analysis. The International Union of Pure and Applied Chemistry Warner, R. K.; Aust. J. Appl. Sci. 4, 581-9 (1953). paper 75-52-5 1 CH3NO2 InChI=1S/CH3NO2/c1-2(3)4/h1H3 LYGJENNIWJXYER-UHFFFAOYSA-N 61.04 Nitromethane Synthesized by standard method; thoroughly dried and fractionally distilled. 13520-83-7 2 UO2(NO3)2(6H2O) InChI=1S/2HNO3.6H2O.2O.U/c2*2-1(3)4;;;;;;;;;/h2*(H,2,3,4);6*1H2;;; WRIBVRZWDPGVQH-UHFFFAOYSA-N 0.0 Uranyl nitrate hexahydrate Source not specified; A.R. grade; not purified. Nitromethane with Uranyl nitrate hexahydrate