Adam Skrzecz 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 4.875e-01 Mole fraction - Liquid (1) 4 4.875 1 -2 4.25e-02 Mole fraction - Liquid (2) 3 4.25 1 1 -1 7.487e-01 Mass fraction (1) 4 7.487 1 -2 7.59e-02 Mass fraction (2) 3 7.59 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 4.890e-01 Mole fraction - Liquid (1) 4 4.890 1 -2 4.69e-02 Mole fraction - Liquid (2) 3 4.69 1 2 -1 7.451e-01 Mass fraction (1) 4 7.451 1 -2 8.31e-02 Mass fraction (2) 3 8.31 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 5.055e-01 Mole fraction - Liquid (1) 4 5.055 1 -1 1.087e-01 Mole fraction - Liquid (2) 4 1.087 1 3 -1 6.966e-01 Mass fraction (1) 4 6.966 1 -1 1.742e-01 Mass fraction (2) 4 1.742 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 4.980e-01 Mole fraction - Liquid (1) 4 4.980 1 -1 1.840e-01 Mole fraction - Liquid (2) 4 1.840 1 4 -1 6.310e-01 Mass fraction (1) 4 6.310 1 -1 2.711e-01 Mass fraction (2) 4 2.711 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 4.193e-01 Mole fraction - Liquid (1) 4 4.193 1 -1 3.607e-01 Mole fraction - Liquid (2) 4 3.607 1 5 -1 4.700e-01 Mass fraction (1) 4 4.700 1 -1 4.701e-01 Mass fraction (2) 4 4.701 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 2.902e-01 Mole fraction - Liquid (1) 4 2.902 1 -1 5.827e-01 Mole fraction - Liquid (2) 4 5.827 1 6 -1 2.906e-01 Mass fraction (1) 4 2.906 1 -1 6.784e-01 Mass fraction (2) 4 6.784 1 1 6.0e+01 Ambient temperature 2 6.0 °C 2 3.332e+02 Ambient temperature 4 3.332 K -1 1.010e-01 Mole fraction - Liquid (1) 4 1.010 1 -1 8.340e-01 Mole fraction - Liquid (2) 4 8.340 1 7 -2 9.30e-02 Mass fraction (1) 3 9.30 1 -1 8.925e-01 Mass fraction (2) 4 8.925 1 1 Solubility, Solubility data series The titration method was used. The composition of the organic-rich phase was presented; the composition of the water-rich phase was not investigated. The International Union of Pure and Applied Chemistry Morozov, A. V.; Sarkisov, A. G.;Turovskii, V. B.; Ilyaskin, V. I.; Dep. Doc. VINITI 102-78, 1 (1978). paper 71-36-3 1 C4H10O InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3 LRHPLDYGYMQRHN-UHFFFAOYSA-N 74.1216 1-Butanol Source not specified; dried, distilled, n(20°C,D)=1.3991, d(25°C,4°C)=0.8010. 110-54-3 2 C6H14 InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3 VLKZOEOYAKHREP-UHFFFAOYSA-N 86.1754 Hexane Source not specified; twice distilled, n(20°C,D)=1.3748, d(25°C,4°C)=0.6544. 7732-18-5 3 H2O InChI=1S/H2O/h1H2 XLYOFNOQVPJJNP-UHFFFAOYSA-N 18.0153 Water Doubly distilled. 1-Butanol with n-Hexane and Water