<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>-3</exponent>
    <number>7.435e-03</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.435</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>-1</exponent>
    <number>7.435e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.435</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.3613e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>5</sigfigs>
    <significand>1.3613</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>-3</exponent>
    <number>7.137e-03</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.137</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>-1</exponent>
    <number>7.137e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.137</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.3069e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>5</sigfigs>
    <significand>1.3069</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>-3</exponent>
    <number>6.13e-03</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>6.13</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>-1</exponent>
    <number>6.130e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>6.130</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.1216e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>5</sigfigs>
    <significand>1.1216</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 deionized water and sealed. Measured volumes of 1,1-dichloroethane were injected into the bottles through each bottle septum using a microliter syringe. The solute 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 three weeks. Samples were then injected into a gas chromatograph equipped with a Carbopack column and a FID detector.The GC responses were compared with calibration plots to establish concentrations.</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>75-34-3</casrn>
  <constituent>1</constituent>
  <formula>C2H4C12</formula>
  <inchi>InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3</inchi>
  <inchikey>SCYULBFZEHDVBN-UHFFFAOYSA-N</inchikey>
  <molweight>98.9592</molweight>
  <name>1,1-Dichloroethane</name>
  <sample>Probable a commercial reagent at least 99% pure, used as received.</sample>
 </substances>
 <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>
 <system>1,1-Dichloroethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 575) - 1,1-Dichloroethane with Water</title>
</compilation>