Andrzej Maczynski, Z. Maczynska 1 6.77e+01 Ambient temperature 3 6.77 °C 1 6.44e+01 Ambient temperature 3 6.44 °C 1 7.11e+01 Ambient temperature 3 7.11 °C 1 -5 5.90e-05 Mole fraction - Liquid (1) 3 5.90 1 -2 3.48e-02 Relative mass - solution (1) 3 3.48 g₁/100 g sln 2 1.073e+02 Ambient temperature 4 1.073 °C 2 1.056e+02 Ambient temperature 4 1.056 °C 2 1.090e+02 Ambient temperature 4 1.090 °C 2 -4 1.127e-04 Mole fraction - Liquid (1) 4 1.127 1 -2 6.64e-02 Relative mass - solution (1) 3 6.64 g₁/100 g sln 2 1.242e+02 Ambient temperature 4 1.242 °C 2 1.227e+02 Ambient temperature 4 1.227 °C 2 1.256e+02 Ambient temperature 4 1.256 °C 3 -4 1.749e-04 Mole fraction - Liquid (1) 4 1.749 1 -1 1.031e-01 Relative mass - solution (1) 4 1.031 g₁/100 g sln 2 1.642e+02 Ambient temperature 4 1.642 °C 2 1.627e+02 Ambient temperature 4 1.627 °C 2 1.656e+02 Ambient temperature 4 1.656 °C 4 -4 4.265e-04 Mole fraction - Liquid (1) 4 4.265 1 -1 2.509e-01 Relative mass - solution (1) 4 2.509 g₁/100 g sln 2 1.864e+02 Ambient temperature 4 1.864 °C 2 1.856e+02 Ambient temperature 4 1.856 °C 2 1.873e+02 Ambient temperature 4 1.873 °C 5 -4 7.825e-04 Mole fraction - Liquid (1) 4 7.825 1 -1 4.595e-01 Relative mass - solution (1) 4 4.595 g₁/100 g sln 2 1.899e+02 Ambient temperature 4 1.899 °C 2 1.878e+02 Ambient temperature 4 1.878 °C 2 1.900e+02 Ambient temperature 4 1.900 °C 6 -4 7.762e-04 Mole fraction - Liquid (1) 4 7.762 1 -1 4.559e-01 Relative mass - solution (1) 4 4.559 g₁/100 g sln 2 2.666e+02 Ambient temperature 4 2.666 °C 2 2.644e+02 Ambient temperature 4 2.644 °C 2 2.689e+02 Ambient temperature 4 2.689 °C 7 -3 4.956e-03 Mole fraction - Liquid (1) 4 4.956 1 0 2.852e+00 Relative mass - solution (1) 4 2.852 g₁/100 g sln 2 2.706e+02 Ambient temperature 4 2.706 °C Ambient temperature °C - 2 2.706e+02 Ambient temperature 4 2.706 °C 8 -3 5.00e-03 Mole fraction - Liquid (1) 3 5.00 1 0 2.88e+00 Relative mass - solution (1) 3 2.88 g₁/100 g sln 1 Solubility, Solubility data series Mixture of (1) and (2) were carefully weighed into glass ampoules. The ampoules were sealed allowing just enough space for thermal expansion. The ampoule, observed through a telescope from behind a safety barrier, was suspended in a 4-liter stirred silicone oil bath, and the bath was heated until the (1) dissolved. On cooling, a cloud of fine (1) droplets appeared, making the suspension opaque. The temperature was raised until the cloud disappeared. The cycle was repeated three to four times until reliable appearance and dissapearance temperatures for the cloud were recorded. The International Union of Pure and Applied Chemistry Pryor, W. A.; Jentoft, R. E.; J. Chem. Eng. Data 1961, 6, 36-7. paper https://doi.org/10.1021/je60009a011 108-38-3 1 C8H10 InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3 IVSZLXZYQVIEFR-UHFFFAOYSA-N 106.165 1,3-Dimethylbenzene Source not specified; 99.8% by freezing point; main impurities are isomeric xylenes; used as received. 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water not specified. m-Xylene with Water