<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>-1</exponent>
    <number>1.010e-01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.010</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>1.15e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.15</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-2</exponent>
    <number>1.06e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.06</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Samples of the organic-water solutions were equilibrated in isothermal waterbaths. A solute isopiestic apparatus was used which has been described elsewhere [1]. The water solubilities were determined using a Beckman Model KF-3 Aquameter.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Christian, S. D.; Affsprung, H. E.; Johnson,J. R.; Worley, J. D.; J. Chem. Educ. 1963, 40, 419.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ed040p419</url>
 </reference>
 <sources>
  <citation>Johnson, J. R.; Christian, S. D.; Affsprung, H. E.; J. Chem. Soc. A. 1966, 77-8.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1039/j19660000077</url>
 </sources>
 <substances>
  <casrn>79-34-5</casrn>
  <constituent>2</constituent>
  <formula>C2H2C14</formula>
  <inchi>InChI=1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H</inchi>
  <inchikey>QPFMBZIOSGYJDE-UHFFFAOYSA-N</inchikey>
  <molweight>167.849</molweight>
  <name>1,1,2,2-Tetrachloroethane</name>
  <sample>Source not given. Reagent grade, distilled in an Oldershaw column before use.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>1</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Distilled (compiler).</sample>
 </substances>
 <system>Water with 1,1,2,2-Tetrachloroethane</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 508) - Water with 1,1,2,2-Tetrachloroethane</title>
</compilation>