<compilation>
 <compilers>Adam Skrzecz</compilers>
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    <property>Mass fraction (2)</property>
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    <property>Ambient temperature</property>
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    <property>Ambient temperature</property>
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    <unit>$\pu{K}$</unit>
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   <data>
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    <property>Mass fraction (2)</property>
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    <number>2.84e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>2.84</significand>
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   <conditions>
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   <data>
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    <property>Mole fraction - Liquid (2)</property>
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    <property>Mass fraction (2)</property>
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    <number>3.22e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.22</significand>
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   <conditions>
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    <property>Ambient temperature</property>
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    <unit>$\pu{K}$</unit>
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   <data>
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    <property>Mass fraction (2)</property>
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    <significand>9.8148</significand>
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    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>4.46</significand>
    <unit>&amp;deg;C</unit>
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   <conditions>
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    <property>Ambient temperature</property>
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    <unit>$\pu{K}$</unit>
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   <data>
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    <property>Mole fraction - Liquid (1)</property>
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   <data>
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    <property>Mole fraction - Liquid (2)</property>
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   <pntnum>18</pntnum>
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    <property>Mass fraction (1)</property>
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    <property>Mass fraction (2)</property>
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    <number>5.20e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>5.20</significand>
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   <conditions>
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    <property>Ambient temperature</property>
    <sigfigs>5</sigfigs>
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    <property>Mass fraction (1)</property>
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    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
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    <property>Ambient temperature</property>
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    <property>Ambient temperature</property>
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    <property>Ambient temperature</property>
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    <significand>4.11</significand>
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  <points>
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  <points>
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   <supplemental>
    <exponent>-1</exponent>
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  </points>
  <series>1</series>
  <title>Compositions along the saturation curve</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The synthetic method was used. Mixtures were prepared in sealed tubes; water was added from a weighed pipette to a known mass of alcohol-benzene mixture.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Staveley, L. A. K.; Johns, R. G. S.; Moore, B. C.; J. Chem. Soc. 1951, 2516-23.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1039/jr9510002516</url>
 </sources>
 <substances>
  <casrn>67-56-1</casrn>
  <constituent>1</constituent>
  <formula>CH4O</formula>
  <inchi>InChI=1S/CH4O/c1-2/h2H,1H3</inchi>
  <inchikey>OKKJLVBELUTLKV-UHFFFAOYSA-N</inchikey>
  <molweight>32.0419</molweight>
  <name>Methanol</name>
  <sample>Source not specified; dried by refluxing over freshly ignited lime, and then with magnesium, distilled.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>3</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>2</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; chemically purified, crystallized, distilled, dried over phosphoric anhydride.</sample>
 </substances>
 <system>Methanol with Benzene and Water</system>
 <title>Solubility data from IUPAC SDS Volume 69 (page ?) - Methanol with Benzene and Water</title>
</compilation>