Valerii P. Sazonov, Nikolai V. Sazonov 1 6.40e+01 Ambient temperature 3 6.40 °C 2 3.372e+02 Ambient temperature 4 3.372 $\pu{K}$ 1 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. 112-92-5 2 C18H38O InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3 GLDOVTGHNKAZLK-UHFFFAOYSA-N 270.494 1-Octadecanol Some alcohols obtained from the Hormel Institute and from Lachat Chemicals; all other alcohols prepared by reduction of the corresponding methyl esters with lithium aluminum hydride; purified by gas-liquid partition chromatography. Acetonitrile with 1-Octadecanol