<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>
   <conditions>
    <exponent>0</exponent>
    <number>7.95e+00</number>
    <property>Mass density</property>
    <sigfigs>3</sigfigs>
    <significand>7.95</significand>
    <unit>g/L</unit>
   </conditions>
   <data></data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>7.973e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>7.973</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-3</exponent>
    <number>1.21e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.21</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>An excess quantity of trichloromethane was added to water and stirred vigorously for 24 hours. After settling at 25 °C for 48 hours, the solution was extracted with cyclohexane. The samples were analyzed using an Aminco-Bowman spectrophotofluorometer. A detailed description of the method has been reported elsewhere [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Mackay, D.; Shiu, W. Y.; J. Chem. Eng. Data. 1977, 22, 399-402.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/je60075a012</url>
 </reference>
 <sources>
  <citation>Hutchinson, T. C.; Hellebust, J. A.; Tam, D.; Mackay, D.; Mascarenhas, R. A.; Shiu, W. Y.; 'Hydrocarbons and Halogenated Hydrocarbons in the Aquatic Environment' Plenum Press, 1980, p. 577-586.</citation>
  <pubtype>chapter</pubtype>
  <url>https://doi.org/10.1007/978-1-4684-3617-4_45</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>Aldrich Chemicals, highest grade, 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>Double distilled.</sample>
 </substances>
 <system>Trichloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Trichloromethane with Water</title>
</compilation>