Valerii P. Sazonov 1 4.45e+01 Ambient temperature 3 4.45 °C 2 3.177e+02 Ambient temperature 4 3.177 $\pu{K}$ 1 1 4.75e+01 Ambient temperature 3 4.75 °C 2 3.207e+02 Ambient temperature 4 3.207 $\pu{K}$ 2 1 5.35e+01 Ambient temperature 3 5.35 °C 2 3.267e+02 Ambient temperature 4 3.267 $\pu{K}$ 3 1 5.95e+01 Ambient temperature 3 5.95 °C 2 3.327e+02 Ambient temperature 4 3.327 $\pu{K}$ 4 1 6.00e+01 Ambient temperature 3 6.00 °C 2 3.332e+02 Ambient temperature 4 3.332 $\pu{K}$ 5 1 6.30e+01 Ambient temperature 3 6.30 °C 2 3.362e+02 Ambient temperature 4 3.362 $\pu{K}$ 6 1 6.35e+01 Ambient temperature 3 6.35 °C 2 3.367e+02 Ambient temperature 4 3.367 $\pu{K}$ 7 1 6.50e+01 Ambient temperature 3 6.50 °C 2 3.382e+02 Ambient temperature 4 3.382 $\pu{K}$ 8 1 6.65e+01 Ambient temperature 3 6.65 °C 2 3.397e+02 Ambient temperature 4 3.397 $\pu{K}$ 9 1 6.75e+01 Ambient temperature 3 6.75 °C 2 3.407e+02 Ambient temperature 4 3.407 $\pu{K}$ 10 1 6.80e+01 Ambient temperature 3 6.80 °C 2 3.412e+02 Ambient temperature 4 3.412 $\pu{K}$ 11 1 6.80e+01 Ambient temperature 3 6.80 °C 2 3.412e+02 Ambient temperature 4 3.412 $\pu{K}$ 12 1 Solubility, Solubility data series The synthetic method was used. A Reichert microscope, type RCH, equipped with a heating stage was used as described in Schmid, et al. [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 75-52-5 1 CH3NO2 InChI=1S/CH3NO2/c1-2(3)4/h1H3 LYGJENNIWJXYER-UHFFFAOYSA-N 61.04 Nitromethane Fisher Scientific Co.; certified, No. N-98; $n_{D}^{20}$ = 1.3820, $\rho^{20} = \pu{1134 g L-1}$. 106-33-2 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-12-13-14(15)16-4-2/h3-13H2,1-2H3 MMXKVMNBHPAILY-UHFFFAOYSA-N 228.371 Ethyl dodecanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 5458-33-3 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-12-13-16-14(15)4-2/h3-13H2,1-2H3 YYOMLCJPYHLLRY-UHFFFAOYSA-N 228.371 Undecyl propanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 5454-09-1 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-13-16-14(15)12-4-2/h3-13H2,1-2H3 PUCQHFICPFUPKW-UHFFFAOYSA-N 228.371 Decyl butanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 487061-22-3 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-12-14(15)16-13-4-2/h3-13H2,1-2H3 ILQYZJGHYZFJPP-UHFFFAOYSA-N 228.371 Undecanoic acid, propyl ester Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 30673-36-0 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-7-8-9-10-11-12-14(15)16-13-6-4-2/h3-13H2,1-2H3 ZRNCNTSXSYXHOW-UHFFFAOYSA-N 228.371 Butyl decanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 4887-30-3 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-7-8-9-11-13-16-14(15)12-10-6-4-2/h3-13H2,1-2H3 CMNMHJVRZHGAAK-UHFFFAOYSA-N 228.371 Octyl hexanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. 1117-55-1 2 C14H28O2 InChI=1S/C14H28O2/c1-3-5-7-9-10-12-14(15)16-13-11-8-6-4-2/h3-13H2,1-2H3 PBGWNXWNCSSXCO-UHFFFAOYSA-N 228.371 Hexyl octanoate Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified. Nitromethane with Esters (C14)