<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>7.5e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>7.5</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>8.0e-02</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>2</sigfigs>
    <significand>8.0</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.139e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.139</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>5.278e-03</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>5.278</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>5.61e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>5.61</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>8.0e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>8.0</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.7e-01</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>2</sigfigs>
    <significand>1.7</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.216e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.216</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-2</exponent>
    <number>1.116e-02</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.116</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A flask was charged with a trichloromethane and water mixture of approximately the desired composition. The system was allowed to equilibrate in a water bath at the desired temperature. Samples were withdrawn from the two layers and concentrations were determined. The analytical techniques are described elsewhere [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Conti, J. J.; Othmer, D. F. Unpublished data.</citation>
  <pubtype>unpublished</pubtype>
 </reference>
 <sources>
  <citation>Conti, J. J.; Othmer, D. F.; Gilmont, R.; J. Chem. Eng. Data 1960, 5, 301-7.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/je60007a019</url>
 </sources>
 <substances>
  <casrn>67-66-3</casrn>
  <constituent>1</constituent>
  <formula>CHCl3</formula>
  <inchi>InChI=1S/CHCl3/c2-1(3)4/h1H</inchi>
  <inchikey>HEDRZPFGACZZDS-UHFFFAOYSA-N</inchikey>
  <molweight>119.378</molweight>
  <name>Trichloromethane</name>
  <sample>U. S. P. grade. Washed with $\ce{H2SO4}$ and $\ce{K2CO3}$ solutions and then distilled. Only the center cut was used.</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>Deionized, distilled twice before use.</sample>
 </substances>
 <system>Trichloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Trichloromethane with Water</title>
</compilation>