<compilation>
 <compilers>Andrzej Maczynski, Z. Maczynska</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Equilibration of (1) and (2) was allowed to take place for at least two days. The organic phase was analyzed for water by the Karl Fischer method.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Masterton, W. L.; Gendrano, M. C.; J. Phys. Chem. 1966, 70, 2895-8.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100881a029</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>not specified.</sample>
 </substances>
 <substances>
  <casrn>71-43-2</casrn>
  <constituent>1</constituent>
  <formula>C6H6</formula>
  <inchi>InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H</inchi>
  <inchikey>UHOVQNZJYSORNB-UHFFFAOYSA-N</inchikey>
  <molweight>78.1118</molweight>
  <name>Benzene</name>
  <sample>source not specified; free from thiophene; used as received.</sample>
 </substances>
 <system>Benzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 145) - Benzene with Water</title>
</compilation>