<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>0</exponent>
    <number>8.7e+00</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>8.7</significand>
    <unit>mol/m3</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>9.96e-03</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.96</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>8.5e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>2</sigfigs>
    <significand>8.5</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A bottle containing a mixture of 50 mL tetrachloromethane and 6 mL water was submerged into a water thermostat bath for two days. The concentration of water in the organic phase was determined by a conventional Karl Fischer deadstop backtitration. The determination was carried out in triplicate. A detailed description of the complete procedure is given in a Ph.D. thesis [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Kirchnerova, J.; Ph. D. Thesis, McGill Univ.; Montreal, Quebec, April 1975, 280 pp.</citation>
  <pubtype>thesis</pubtype>
 </reference>
 <sources>
  <citation>Kirchnerová, J.; Cave, G. C. B.; Can. J. Chem. 1976, 54(24), 3909-16.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1139/v76-562</url>
 </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>Fisher - C199, washed with $\ce{H2SO4}$ and $\ce{K2CO3}$ solutions and finally with water. Dried over silica gel and fractionally distilled. Purity was better than 99.8%.</sample>
 </substances>
 <substances>
  <casrn>56-23-5</casrn>
  <constituent>1</constituent>
  <formula>CCl4</formula>
  <inchi>InChI=1S/CCl4/c2-1(3,4)5</inchi>
  <inchikey>VZGDMQKNWNREIO-UHFFFAOYSA-N</inchikey>
  <molweight>153.823</molweight>
  <name>Tetrachloromethane</name>
  <sample>Distilled and deionized.</sample>
 </substances>
 <system>Tetrachloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Tetrachloromethane with Water</title>
</compilation>