<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>2.959e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>2.959</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>2.90e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.90</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>3.51e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.51</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>4.234e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>4.234</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>4.11e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>4.11</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>4.506e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>4.506</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>5.567e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>5.567</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>5.35e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.35</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Equilibrium experiments were carried out in a constant temperature water bath using a stirrer. An equilibration period of at least five days was allowed. The total water content in the organic phase was determined by a Karl Fischer titration. Each reported water solubility was obtained as an average of at least two independent determinations.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Goldman, S.; Ph.D. Dissertation, McGill University, Montreal, Canada 1969, p 84.</citation>
  <pubtype>dissertation</pubtype>
 </sources>
 <substances>
  <casrn>108-90-7</casrn>
  <constituent>1</constituent>
  <formula>C6H5C1</formula>
  <inchi>InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H</inchi>
  <inchikey>MVPPADPHJFYWMZ-UHFFFAOYSA-N</inchikey>
  <molweight>112.557</molweight>
  <name>Chlorobenzene</name>
  <sample>Distilled.</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>Reagent grade, washed with conc. $\ce{H2SO4}$ and with 1 M $\ce{NaHCO3}$ and then fractionally distilled over silica gel.</sample>
 </substances>
 <system>Chlorobenzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 20 (page 173) - Chlorobenzene with Water</title>
</compilation>