<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>1.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>1.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>0</exponent>
    <number>5.9e+00</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>5.9</significand>
    <unit>mol/m3</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>6.64e-03</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>6.64</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>5.66e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.66</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <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>2</pntnum>
   <supplemental>
    <exponent>-3</exponent>
    <number>9.89e-03</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.89</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>8.44e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.44</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The solute isopiestic method was used without modification. The apparatus employed consisted of a closed vessel divided into two compartments, one for water and the other for the organic solvent. Equilibrium was attained often for a period of 6 to 8 hours. The solution was analyzed for water with the Beckman KF-3 Aquameter. The Karl Fisher reagent was standardized against crystalline sodium tartarate dihydrate.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Christian, S. D.; Affsprung, H. E.; Hunter, W. J. A.; Gillam, W. S.; McCoy, W. H.; 'Solute Properties of Water', U.S. Office of Saline Water Research and Development Program, Report No. 301 1968, p. 71, 79.</citation>
  <pubtype>report</pubtype>
 </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>Source not given, certified or reagent grade, distilled through a 30 plate Oldershaw column before use.</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.</sample>
 </substances>
 <system>Tetrachloromethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Tetrachloromethane with Water</title>
</compilation>