<compilation>
 <compilers>M. Elizabeth Derrick, H. Lawrence Clever</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.9815e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>5</sigfigs>
    <significand>2.9815</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>4.39e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>4.39</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>2.63e+00</number>
    <property>Ostwald coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>2.63</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>2.41e+00</number>
    <property>Bunsen Coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>2.41</significand>
    <unit>$\pu{cm3(g) cm-3(l) atm-1}$</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A commercial Van Slyke blood gas apparatus (E. H. Sargent Co.) was modified by the authors. The total pressure of the gas and the solvent vapor in the solution chamber was adjusted to a pressure of 1 atm. The pressure was maintained at 1 atm during the solution process. The saturated solution was transferred to a bulb below the lower stopcock of the extraction vessel and sealed off. The gas and solvent vapor were then brought to volume over mercury. See [2] for details of the extraction procedure.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Peters, J. P.; Van Slyke, D. D.; Quantitative Clinical Chemistry, Baltimore, MD, 1932, Volume II.</citation>
  <pubtype>book</pubtype>
 </reference>
 <sources>
  <citation>Boyer, F. L.; Bircher, L. J.; J. Phys. Chem. 1960, 64, 1330 - 1331.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100838a501</url>
 </sources>
 <substances>
  <casrn>74-85-1</casrn>
  <constituent>1</constituent>
  <formula>C2H4</formula>
  <inchi>InChI=1S/C2H4/c1-2/h1-2H2</inchi>
  <inchikey>VGGSQFUCUMXWEO-UHFFFAOYSA-N</inchikey>
  <molweight>28.0532</molweight>
  <name>Ethene</name>
  <sample>Ethene. Matheson Co. Stated to be 99.5 mol%.</sample>
 </substances>
 <substances>
  <casrn>67-56-1</casrn>
  <constituent>2</constituent>
  <formula>CH4O</formula>
  <inchi>InChI=1S/CH4O/c1-2/h2H,1H3</inchi>
  <inchikey>OKKJLVBELUTLKV-UHFFFAOYSA-N</inchikey>
  <molweight>32.0419</molweight>
  <name>Methanol</name>
  <sample>Methanol. Source not given. Treated by standard methods to remove aldehydes and ketones, then dried and distilled.</sample>
 </substances>
 <system>Ethene with Methanol</system>
 <title>Solubility data from IUPAC SDS Volume 57 (page ?) - Ethene with Methanol</title>
</compilation>