<compilation>
 <compilers>Andrzej Maczynski, Z. Maczynska</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A small excess of (1) was equilibrated with (2) by shaking at 20 °C until saturation was attained. The saturated aqueous phase was analysed by ultraviolet spectrophotometry.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Corby, T. C.; Elworthy, P. H.; J. Pharm. Pharmacol. 1971, 23 suppl. 39 S-48 S.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1111/j.2042-7158.1971.tb08767.x</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>Distilled once from glass.</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>W. Jarvie Ltd., crystalizable; distilled before use; $n_{D}^{18}$ 1.5028.</sample>
 </substances>
 <system>Benzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 154) - Benzene with Water</title>
</compilation>