<compilation>
 <compilers>Andrzej Maczynski</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Saturated solutions of tritum labeled (2) in (1) were prepared in two ways. In the first, nitrogen was passed throught the vessel with (2) and next through the vessel with (1) and frozen. In the second, about 500 mL of (1) and 1 mL (2) were stirred. The concentration of (2) in (1) was calculated from scintillation measurements.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Zel'venskii, Ya. D.; Efremov, A. A.; Larin, G. M.; Chem. Technol. Fuels Oils 1965, 1(7) 506.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1007/bf00731391</url>
 </sources>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>2</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Source not specified; commercial; 1 Ci/mL HTO used as received.</sample>
 </substances>
 <substances>
  <casrn>110-82-7</casrn>
  <constituent>1</constituent>
  <formula>C6H12</formula>
  <inchi>InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2</inchi>
  <inchikey>XDTMQSROBMDMFD-UHFFFAOYSA-N</inchikey>
  <molweight>84.1595</molweight>
  <name>Cyclohexane</name>
  <sample>Source not specified; pure grade; shaken with conc. $\ce{H2SO4}$ + $\ce{HNO3}$; washed with water, dried over sodium, and distilled; purity not specified. BP = 80.82&amp;deg;C.</sample>
 </substances>
 <system>Cyclohexane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 239) - Cyclohexane with Water</title>
</compilation>