<compilation>
 <compilers>Andrzej Maczynski, Z. Maczynska, A. Szafranski</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A mixture of (1) and (2) was equilibrated at 25 ± 0.1 °C for a minimum of 12 hrs in a 200-mL Teflon-stoppered vessel (25 cm long and 3.5 cm across) with gentle shaking, allowed to settle for 6 hrs and tested for the absence of emulsion (Tyndall effect). The aqueous and organic phases were analyzed by GLC with internal standardization) on a Hewlett-Packard Model 700 instrument equipped with a 15% SE-30 on 60/80 mesh acid-washed $\ce{(CH3)2Cl2Si}$-treated Chromosorb P column (steel capillary 10 ft x 0.125 inch). The (1) in the aqueous phase was extracted into 5 mL of heptane and the extract analyzed by glc.</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>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>
 <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>Phillip Petroleum Co. research grade, 99+ mole%; used as received.</sample>
 </substances>
 <system>Benzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 160) - Benzene with Water</title>
</compilation>