Valerii P. Sazonov 2 1.145e+02 Ambient temperature 4 1.145 °C 2 3.877e+02 Ambient temperature 4 3.877 $\pu{K}$ 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.; Microchem. J. 7, 287-96 (1963). paper https://doi.org/10.1016/0026-265x(63)90053-5 Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; Microchem. J. 7, 297-302 (1963). paper https://doi.org/10.1016/0026-265x(63)90054-7 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 C51H92O6 801.3 1,2,3-Tri(cis-9-hexadecenoyloxy)propane Monoacid triglycerides obtained from the Hormel Foundation, other triglycerides from Procter & Gamble Co.; purity verified by thin-layer adsorption chromatography. Acetonitrile with 1,2,3-Tri(cis-9-hexadecenoyloxy)propane