<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>1.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>1.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-4</exponent>
    <number>1.52e-04</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.52</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>1.52e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.52</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>2.825e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>2.825</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-4</exponent>
    <number>2.73e-04</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.73</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>2.73e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.73</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>5.075e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>5.075</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <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>-4</exponent>
    <number>1.76e-04</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.76</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>1.76e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.76</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>3.271e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>3.271</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>250 cm&lt;sup&gt;3&lt;/sup&gt; bottles were filled with distilled and deionized water and sealed. A measured volume of cis-1,2-dichloroethene was injected into the bottles through each septum using a microliter syringe. The cis-1,2-dichloroethene was in excess of the anticipated solubility limit. The bottles were shaken for 1 hour with a wrist-action shaker and allowed to equilibrate for about 3 weeks. Samples were then injected into a gas chromatograph equipped with a Carbopac Column and a FIDdetector. The GC response was compared with calibration plots.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Howe, G. B.; Mullins, M. E.; Rogers, T. N.; AFESC Tyndall Air Force Base, Report ESL-TR-86-66, Vol. 1, Florida, Sept. 1987, 86 pp. (AD-A188 571).</citation>
  <pubtype>report</pubtype>
 </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>156-59-2</casrn>
  <constituent>1</constituent>
  <formula>C2H2Cl2</formula>
  <inchi>InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-</inchi>
  <inchikey>KFUSEUYYWQURPO-UPHRSURJSA-N</inchikey>
  <molweight>96.9433</molweight>
  <name>cis-1,2-Dichloroethene</name>
  <sample>Probably a commercial reagent at least 99% pure, used as received.</sample>
 </substances>
 <system>cis-1,2-Dichloroethene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 493) - cis-1,2-Dichloroethene with Water</title>
</compilation>