<compilation>
 <compilers>Ari L. Horvath</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>-1</exponent>
    <number>3.7e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>3.7</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>4.87e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>4.87</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>2.69e-05</number>
    <property>Mole (1) per 100 gram</property>
    <sigfigs>3</sigfigs>
    <significand>2.69</significand>
    <unit>mol/g</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>-1</exponent>
    <number>2.5e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>2.5</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>3.29e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>3.29</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>1.82e-05</number>
    <property>Mole (1) per 100 gram</property>
    <sigfigs>3</sigfigs>
    <significand>1.82</significand>
    <unit>mol/g</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>-1</exponent>
    <number>1.6e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>1.6</significand>
    <unit>1</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>2.10e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.10</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>1.17e-05</number>
    <property>Mole (1) per 100 gram</property>
    <sigfigs>3</sigfigs>
    <significand>1.17</significand>
    <unit>mol/g</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>7.0e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>7.0</significand>
    <unit>1</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental>
    <exponent>-5</exponent>
    <number>9.19e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.19</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-6</exponent>
    <number>5.10e-06</number>
    <property>Mole (1) per 100 gram</property>
    <sigfigs>3</sigfigs>
    <significand>5.10</significand>
    <unit>mol/g</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The organic compound was condensed into a degassed liquid water sample up to saturation at which two phases appeared. After shaking the mixture for several hours, equilibrium was achieved and the respective phases were analysed in a gas chro-matograph. The original report is not obtainable; therefore, the details were taken from Junge [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Junge, C.; Z. Naturforsch. A 1976, 31, 482.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1515/zna-1976-0510</url>
 </reference>
 <sources>
  <citation>Zeininger, H.; Hoechst A. G.; Internat Report, 1975.</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 (compiler).</sample>
 </substances>
 <substances>
  <casrn>75-69-4</casrn>
  <constituent>1</constituent>
  <formula>CCl3F</formula>
  <inchi>InChI=1S/CCl3F/c2-1(3,4)5</inchi>
  <inchikey>CYRMSUTZVYGINF-UHFFFAOYSA-N</inchikey>
  <molweight>137.368</molweight>
  <name>Trichlorofluoromethane</name>
  <sample>Source and purity not given.</sample>
 </substances>
 <system>Trichlorofluoromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Trichlorofluoromethane with Water</title>
</compilation>