<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <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></data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>8.05e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.05</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>9.44e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.44</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>0</exponent>
    <number>1.05e+00</number>
    <property>Ostwald coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>1.05</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>3.7e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>3.7</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>6.82e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>6.82</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>7.99e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>7.99</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>4.5e-01</number>
    <property>Ostwald coefficient</property>
    <sigfigs>2</sigfigs>
    <significand>4.5</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A tetrachloromethane - air mixture was bubbled through 50 mL distilled water contained in a gas absorption bottle with a sintered glass plate. Equilibrium was reached in 3/4 hour with a gas flow of 50 mL/mim. The saturated solution was transferred to a measuring cylinder and shaken with toluene. The toluene extraction was allowed to settle and then analyzed for tetrachloromethane by the addition of pyridine and alkali; see [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Habgood, S.; Powell, J. F.; Br. J. Industr. Med. 1944, 1, 39.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1136/oem.2.1.39</url>
 </reference>
 <sources>
  <citation>Powell, J. F.; Br. J. Industr. Med. 1945, 2, 212-6.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1136/oem.2.4.212</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>distilled.</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>Source and purity not given.</sample>
 </substances>
 <system>Tetrachloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Tetrachloromethane with Water</title>
</compilation>