<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>0</exponent>
    <number>1.10e+00</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.10</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.8e-01</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>2</sigfigs>
    <significand>1.8</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>2.02e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.02</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>9.81e-03</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>9.81</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The mutual solubility data were determined by a method described by Othmer, et al. [1]. A 10 mL 1,2-dichloroethane sample was added to water from a buret and agitated until the solution became turbid. The appearance of the turbidity indicated the formation of a second phase. The solubility was calculated using the known densities and volumes.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Othmer, D. F.; White, R. E.; Trueger, E.; Ind. Eng. Chem. 1941, 33(10), 1240-8.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ie50382a007</url>
 </reference>
 <sources>
  <citation>Coca, J.; Diaz, R. M.; Pazos, C.; Fluid Phase Equilib. 1980, 4, 123-136.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0378-3812(80)80010-0</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>Distilled.</sample>
 </substances>
 <substances>
  <casrn>107-06-2</casrn>
  <constituent>1</constituent>
  <formula>C2H4Cl2</formula>
  <inchi>InChI=1S/C2H4Cl2/c3-1-2-4/h1-2H2</inchi>
  <inchikey>WSLDOOZREJYCGB-UHFFFAOYSA-N</inchikey>
  <molweight>98.9592</molweight>
  <name>1,2-Dichloroethane</name>
  <sample>Probus Chemicals reagent, further purified by distillation in a heli-packing column.</sample>
 </substances>
 <system>1,2-Dichloroethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 601) - 1,2-Dichloroethane with Water</title>
</compilation>