Valerii P. Sazonov 1 2.25e+01 Ambient temperature 3 2.25 °C 2 2.957e+02 Ambient temperature 4 2.957 $\pu{K}$ 1 1 2.90e+01 Ambient temperature 3 2.90 °C 2 3.022e+02 Ambient temperature 4 3.022 $\pu{K}$ 2 1 3.50e+01 Ambient temperature 3 3.50 °C 2 3.082e+02 Ambient temperature 4 3.082 $\pu{K}$ 3 1 3.95e+01 Ambient temperature 3 3.95 °C 2 3.127e+02 Ambient temperature 4 3.127 $\pu{K}$ 4 1 4.50e+01 Ambient temperature 3 4.50 °C 2 3.182e+02 Ambient temperature 4 3.182 $\pu{K}$ 5 1 5.00e+01 Ambient temperature 3 5.00 °C 2 3.232e+02 Ambient temperature 4 3.232 $\pu{K}$ 6 1 5.55e+01 Ambient temperature 3 5.55 °C 2 3.287e+02 Ambient temperature 4 3.287 $\pu{K}$ 7 1 6.60e+01 Ambient temperature 3 6.60 °C 2 3.392e+02 Ambient temperature 4 3.392 $\pu{K}$ 8 1 Solubility, Solubility data series The synthetic method was used. A Reichert microscope, type RCH, equipped with a heating stage was used as described elsewhere [1]. The disappearance and reappearance of the interface between (1) and (2) could be observed without difficulty. The International Union of Pure and Applied Chemistry Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; J. Am. Oil Chem. Soc. 42, 372 (1965). paper https://doi.org/10.1007/bf02635572 Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; Microchem. J. 9, 134-144 (1965). paper https://doi.org/10.1016/0026-265x(65)90094-9 75-05-8 1 C2H3N InChI=1S/C2H3N/c1-2-3/h1H3 WEVYAHXRMPXWCK-UHFFFAOYSA-N 41.052 Acetonitrile Baker Chemical Co.; reagent No. 9011; $n_{D}^{20}$ = 1.3445, $d_{4}^{20}$ = 0.780. 2 C11H24O - C19H40O 0.0 2-Alcohols (C11-C19) Some alcohols obtained from Aldrich Chemical Co.; all other alcohols prepared by reduction of the corresponding methyl ketones with lithium aluminum hydride; purified by gas-liquid partition chromatography. Acetonitrile with 2-Alcohols