Andrzej Maczynski 0 6.3e+00 Ambient temperature 2 6.3 °C 1 -10 6.61e-10 Mole fraction - Liquid (1) 3 6.61 1 -7 7.06e-07 Relative mass - solution (1) 3 7.06 g₁/100 g sln 0 9.1e+00 Ambient temperature 2 9.1 °C 2 -10 7.94e-10 Mole fraction - Liquid (1) 3 7.94 1 -7 8.48e-07 Relative mass - solution (1) 3 8.48 g₁/100 g sln 1 1.08e+01 Ambient temperature 3 1.08 °C 3 -10 8.83e-10 Mole fraction - Liquid (1) 3 8.83 1 -7 9.43e-07 Relative mass - solution (1) 3 9.43 g₁/100 g sln 1 1.39e+01 Ambient temperature 3 1.39 °C 4 -9 1.04e-09 Mole fraction - Liquid (1) 3 1.04 1 -6 1.11e-06 Relative mass - solution (1) 3 1.11 g₁/100 g sln 1 1.83e+01 Ambient temperature 3 1.83 °C 5 -9 1.36e-09 Mole fraction - Liquid (1) 3 1.36 1 -6 1.45e-06 Relative mass - solution (1) 3 1.45 g₁/100 g sln 1 2.31e+01 Ambient temperature 3 2.31 °C 6 -9 1.79e-09 Mole fraction - Liquid (1) 3 1.79 1 -6 1.91e-06 Relative mass - solution (1) 3 1.91 g₁/100 g sln 1 2.50e+01 Ambient temperature 3 2.50 °C 7 -9 1.99e-09 Mole fraction - Liquid (1) 3 1.99 1 -6 2.13e-06 Relative mass - solution (1) 3 2.13 g₁/100 g sln 1 2.70e+01 Ambient temperature 3 2.70 °C 8 -9 2.27e-09 Mole fraction - Liquid (1) 3 2.27 1 -6 2.42e-06 Relative mass - solution (1) 3 2.42 g₁/100 g sln 1 3.11e+01 Ambient temperature 3 3.11 °C 9 -9 3.01e-09 Mole fraction - Liquid (1) 3 3.01 1 -6 3.21e-06 Relative mass - solution (1) 3 3.21 g₁/100 g sln 1 Solubility, Solubility data series The dynamic coupled column liquid chromatography (DCCLC) method was based on generating saturated solutions by pumping water through a column packed with glass beads that have been coated with the component [1] (generator column). The concentration of [1] in the effluent of the generator column was measured by a modification of the coupled column liquid chromatographic process that has been described in [1]. The International Union of Pure and Applied Chemistry May, W.; Chesler, S.; Cram, S.; Gump, B.; Hertz, H.; Enagonio, D.; Dyszel, S.; J. Chromatogr. Sci. 1975, 13, 535. paper https://doi.org/10.1093/chromsci/13.11.535 May, W. E.; Wasik, S. P.; Freeman, D. H.; Anal. Chem. 1978, 50, 997-1000 paper https://doi.org/10.1021/ac50029a042 7732-18-5 2 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water Distilled over $\ce{KMnO4}$ and $\ce{NaOH}$ and passed through a column packed with XAD-2 (Rohm and Hass, Philadelphia, Pa). 613-12-7 1 C15H12 InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3 GYMFBYTZOGMSQJ-UHFFFAOYSA-N 192.256 2-Methylanthracene Commercial product; less than 3% impurities. 2-Methylanthracene with Water