<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>3.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>3.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>2</exponent>
    <number>7.431e+02</number>
    <property>Mass concentration (m/v) (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.431</significand>
    <unit>g/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>7.458e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.458</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.023e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.023</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Standard trichloroethene solutions of increasing concentration were prepared in volumetric flasks as described elsewhere [1].The aqueous organic liquid phase was 25 mL and the vapor phase above the mixture was 35 mL The system was allowed to reach equilibrium in a constant temperature bath and then a sample was injected into the gas chromatograph. Values reported are an average of at least 5 measurements.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>McNally, M. E.; Grob, R. L.; J. Chromatogr. A 1983, 260, 23-32.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0021-9673(83)80003-x</url>
 </reference>
 <sources>
  <citation>McNally, M. E.; Grob, R. L.; J. Chromatogr. A 1984, 284, 105-16.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/s0021-9673(01)87806-7</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 and run through two Barnstead purification cartridges.</sample>
 </substances>
 <substances>
  <casrn>79-01-6</casrn>
  <constituent>1</constituent>
  <formula>C2HCl3</formula>
  <inchi>InChI=1S/C2HCl3/c3-1-2(4)5/h1H</inchi>
  <inchikey>XSTXAVWGXDQKEL-UHFFFAOYSA-N</inchikey>
  <molweight>131.388</molweight>
  <name>Trichloroethylene</name>
  <sample>Chemical Service, West Chester, PA., USA., purest grade available.</sample>
 </substances>
 <system>Trichloroethene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 466) - Trichloroethene with Water</title>
</compilation>