<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>5.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>5.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-5</exponent>
    <number>1.912e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.912</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.56e-01</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.56</significand>
    <unit>g/kg</unit>
   </data>
   <data>
    <exponent>-3</exponent>
    <number>1.061e-03</number>
    <property>Molality (1 in 2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.061</significand>
    <unit>mol/kg</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>6.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-5</exponent>
    <number>1.998e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.998</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.63e-01</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.63</significand>
    <unit>g/kg</unit>
   </data>
   <data>
    <exponent>-3</exponent>
    <number>1.109e-03</number>
    <property>Molality (1 in 2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.109</significand>
    <unit>mol/kg</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The determination of the solubility was based upon volumetric principles applied to the measurement of excess solute in a calibrated apparatus as described by Rex [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Rex, A.; Z. Phys. Chem. 1906, 55U, 355-70.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1515/zpch-1906-5519</url>
 </reference>
 <sources>
  <citation>Klemenc, A.; Löw, M.; Rec. Trav. Chim. Pays-Bas 1930, 49(4), 629-40.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1002/recl.19300490705</url>
 </sources>
 <substances>
  <casrn>106-46-7</casrn>
  <constituent>1</constituent>
  <formula>C6H4Cl2</formula>
  <inchi>InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H</inchi>
  <inchikey>OCJBOOLMMGQPQU-UHFFFAOYSA-N</inchikey>
  <molweight>147.002</molweight>
  <name>1,4-Dichlorobenzene</name>
  <sample>Prepared by chlorination of benzene using iodine as catalyst. The preparate was recrystalized several times in ethanol before use, MP = 52.7&amp;deg;C.</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.</sample>
 </substances>
 <system>1,4-Dichlorobenzene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 20 (page 101) - 1,4-Dichlorobenzene with Water</title>
</compilation>