<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>-5</exponent>
    <number>1.261e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.261</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.029e-01</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.029</significand>
    <unit>g/kg</unit>
   </data>
   <data>
    <exponent>-4</exponent>
    <number>7.00e-04</number>
    <property>Molality (1 in 2)</property>
    <sigfigs>3</sigfigs>
    <significand>7.00</significand>
    <unit>mol/kg</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Equilibrium was established between the water and the 1,3-dichlorobenzene in a sealed flask [1] with the aid of a magnetic stirrer during 48 hours under isothermal conditions. After the sample was filtered through a glass-wool plug, the 1,3-dichlorobenzene was extracted with 2,2, 4-trimethylpentene. Sample optical densities were determined spectrophotometrically [2]. Five parallel determinations were done. The reported work was based upon a Ph.D. dissertation [3].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Vesala, A.; Ph.D. Dissertation, University of Turku, Turku, 1973.</citation>
  <pubtype>dissertation</pubtype>
 </reference>
 <sources>
  <citation>Vesala, A.; Acta Chem. Scand. 1974, 28A(8), 839-845.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.3891/acta.chem.scand.28a-0839</url>
 </sources>
 <substances>
  <casrn>541-73-1</casrn>
  <constituent>1</constituent>
  <formula>C6H4C12</formula>
  <inchi>InChI=1S/C6H4Cl2/c7-5-2-1-3-6(8)4-5/h1-4H</inchi>
  <inchikey>ZPQOPVIELGIULI-UHFFFAOYSA-N</inchikey>
  <molweight>147.002</molweight>
  <name>1,3-Dichlorobenzene</name>
  <sample>Commercial reagent of analytical grade distilled through a column resulting in a more than 99% pure sample.</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>Distilled, deionized, and degassed.</sample>
 </substances>
 <system>1,3-Dichlorobenzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 20 (page 94) - 1,3-Dichlorobenzene with Water</title>
</compilation>