<compilation>
 <compilers>Colin L. Young</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.8815e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>5</sigfigs>
    <significand>2.8815</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <conditions>
    <exponent>1</exponent>
    <number>1.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>1.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>2.38e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.38</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>4.445e+00</number>
    <property>Ostwald coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>4.445</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>1</exponent>
    <number>4.20e+01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>4.20</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>All glass apparatus used at very low gas partial pressures, containing a replaceable degassed solvent ampule equipped with a breakable point which could be broken by means of a magnetically activated plunger. Quantity of gas fed into system determined by measuring the pressure change in a known volume. Quantity of liquid measured by weight. Pressure change observed after solvent released. Experimental details described by Rzad and Claes, [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Claes, P.; Rzad, S.; Bull. Soc. Chim. Belg. 1964, 73, 689.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1002/bscb.19640730707</url>
 </reference>
 <sources>
  <citation>Tilquin, B.; Decanniere, L.; Fontaine, R.; Claes, P.; Ann. Soc. Sc. Bruxelles 1967, 81, 191-199.</citation>
  <pubtype>paper</pubtype>
 </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>Source not given; minimum purity specified as 99.0 mole%.</sample>
 </substances>
 <substances>
  <casrn>110-54-3</casrn>
  <constituent>2</constituent>
  <formula>C6H14</formula>
  <inchi>InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3</inchi>
  <inchikey>VLKZOEOYAKHREP-UHFFFAOYSA-N</inchikey>
  <molweight>86.1754</molweight>
  <name>Hexane</name>
  <sample>Fluka pure grade; minimum purity specified as 99.0 mole%.</sample>
 </substances>
 <system>Ethene with Hexane</system>
 <title>Solubility data from IUPAC SDS Volume 57 (page 86) - Ethene with Hexane</title>
</compilation>