<compilation>
 <compilers>Marie C. Haulait-Pirson</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A mixture of (1) and (2) was equilibrated for at least 12 hrs in a 200 mL Teflon stoppered vessel with gentle shaking. The solution was allowed to settle for 6 hrs and the aqueous phase was tested (Tyndall effect). Both phases were analyzed by the gas chromatographic technique of internal standardization. The (1) in the aqueous phase was extracted into 5 mL of heptane and the extract analysed by GLC. The instrument was a Hewlett-Packard model equiped with a flame ionization detector.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Leinonen, P. J.; Mackay, D.; Can. J. Chem. Eng. 1973, 51, 230-3.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1002/cjce.5450510213</url>
 </sources>
 <substances>
  <casrn>110-54-3</casrn>
  <constituent>1</constituent>
  <formula>C6H14</formula>
  <inchi>InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3</inchi>
  <inchikey>VLKZOEOYAKHREP-UHFFFAOYSA-N</inchikey>
  <molweight>86.1754</molweight>
  <name>Hexane</name>
  <sample>Phillips Petroleum Co.; research grade; purity 99%+; used without further purification.</sample>
 </substances>
 <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>doubly distilled.</sample>
 </substances>
 <system>Hexane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 344) - Hexane with Water</title>
</compilation>