<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.485e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.485</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>5.046e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>5.046</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>9.410e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>9.410</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-2</exponent>
    <number>1.50e-02</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>1.50</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The original method and apparatus for the determination of Henry's law constants are described elsewhere [1]. The general procedure was to add an excess quantity of 1,1-dichloroethene to distilled deionized water, place the sample in a thermostat bath, and provide overnight mixing. A portion of this solution was returned to the stripping vessel. The 1,1-dichloroethene was stripped isothermally from the solution at a know gas flow rate. The Henry's law constant was calculated fromthe log of the concentration versus time plot. The experimental data values are averages of two or more replicates.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Warner, H. P.; Cohen, J. M.; Ireland, J. C.; 'Determination of Henry's Law Constants of Selected Priority Pollutants' U.S. EPA Technical Report, PB87-212684, Cincinnati, OH.; July 1987.</citation>
  <pubtype>report</pubtype>
  <url>https://ntrl.ntis.gov/NTRL/dashboard/searchResults/titleDetail/PB87212684.xhtml</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 deionized.</sample>
 </substances>
 <substances>
  <casrn>75-35-4</casrn>
  <constituent>1</constituent>
  <formula>C2H2Cl2</formula>
  <inchi>InChI=1S/C2H2Cl2/c1-2(3)4/h1H2</inchi>
  <inchikey>LGXVIGDEPROXKC-UHFFFAOYSA-N</inchikey>
  <molweight>96.9433</molweight>
  <name>1,1-Dichloroethene</name>
  <sample>Purest quality available, used as received, stated purity greater than 99%.</sample>
 </substances>
 <system>1,1-Dichloroethene (1,1-dichloroethylene) with Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 489) - 1,1-Dichloroethene (1,1-dichloroethylene) with Water</title>
</compilation>