<compilation>
 <compilers>Marie C. Haulait-Pirson, Andrzej Maczynski</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>0</exponent>
    <number>0e+00</number>
    <property>Ambient temperature</property>
    <sigfigs>0</sigfigs>
    <significand>0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>4.6e-03</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>2</sigfigs>
    <significand>4.6</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/100 g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.79e-04</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>1.79</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <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>8.6e-03</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>2</sigfigs>
    <significand>8.6</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/100 g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>3.35e-04</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>3.35</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>-2</exponent>
    <number>1.42e-02</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>3</sigfigs>
    <significand>1.42</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/100 g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>5.53e-04</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>5.53</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>-2</exponent>
    <number>2.49e-02</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>3</sigfigs>
    <significand>2.49</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/100 g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>9.69e-04</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>9.69</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>4.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>4.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>3.98e-02</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>3</sigfigs>
    <significand>3.98</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/100 g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>5</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.548e-03</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.548</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
  <title>Solubility of water in cyclopentane</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Component (1) was introduced into a thermostatted flask and saturated for 5 hours with (2). Next, calcium hydride was added and the evolving hydrogen volume measured and hence the concentration of (2) in (1) was evaluated.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Englin, B. A.; Plate, A. F.; Tugolukov, V. M. Pryanishnikova, M. A.; Chem. Technol. Fuels Oils, 1965, 1(9), 722-726.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1007/bf00721855</url>
 </sources>
 <substances>
  <casrn>287-92-3</casrn>
  <constituent>1</constituent>
  <formula>C5H10</formula>
  <inchi>InChI=1S/C5H10/c1-2-4-5-3-1/h1-5H2</inchi>
  <inchikey>RGSFGYAAUTVSQA-UHFFFAOYSA-N</inchikey>
  <molweight>70.1329</molweight>
  <name>Cyclopentane</name>
  <sample>Not specified.</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>not specified.</sample>
 </substances>
 <system>Cyclopentane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 17) - Cyclopentane with Water</title>
</compilation>