<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>7.38e+01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>7.38</significand>
    <unit>mol/m3</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>8.98e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.98</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>5.92e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.92</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Trichloromethane was equilibrated with water in an apparatus described elsewhere [1]. The equilibration was allowed to take place for two days with the entire apparatus immersed in a water bath. The organic phase was analyzed for water by the Karl Fischer method (dead-stop end point). The microburet used for the titration was read to ± 0.01 mL. All titrations were carried out in an atmosphere of dry nitrogen.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Christian, S.; Affsprung, H.; Johanson, J.; J. Chem. Soc. 1963, 1896.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1039/jr9630001896</url>
 </reference>
 <sources>
  <citation>Masterton, W. L.; Gendrano, M. C.; J. Phys. Chem. 1966, 70, 2895-8.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100881a029</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>Distilled.</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>Source not given. Reagent grade, washed with distilled water and the purity was checked with GC.</sample>
 </substances>
 <system>Trichloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Trichloromethane with Water</title>
</compilation>