<compilation>
 <compilers>Colin L. Young</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.982e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.982</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>9.00e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.00</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>4.71e+00</number>
    <property>Henry's Constant (ln)</property>
    <sigfigs>3</sigfigs>
    <significand>4.71</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.982e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.982</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>9.10e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.10</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>4.70e+00</number>
    <property>Henry's Constant (ln)</property>
    <sigfigs>3</sigfigs>
    <significand>4.70</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.982e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.982</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>7.01e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>7.01</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>4.96e+00</number>
    <property>Henry's Constant (ln)</property>
    <sigfigs>3</sigfigs>
    <significand>4.96</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.982e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.982</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>3.182e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>3.182</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>5.75e+00</number>
    <property>Henry's Constant (ln)</property>
    <sigfigs>3</sigfigs>
    <significand>5.75</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.982e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.982</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>1.592e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.592</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>4.14e+00</number>
    <property>Henry's Constant (ln)</property>
    <sigfigs>3</sigfigs>
    <significand>4.14</significand>
    <unit>$\pu{atm}$</unit>
   </data>
   <pntnum>5</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Solubilities were determined by a volumetric method described as 'the Ostwald method'. No other details given.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Brückl, N.; Kim, J. I.; Z. Phys. Chem. 1981, 126, 133-150.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1524/zpch.1981.126.2.133</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>Linde Co. sample, purity 99.8 volume%.</sample>
 </substances>
 <substances>
  <casrn>100-47-0</casrn>
  <constituent>2</constituent>
  <formula>C7H5N</formula>
  <inchi>InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H</inchi>
  <inchikey>JFDZBHWFFUWGJE-UHFFFAOYSA-N</inchikey>
  <molweight>103.121</molweight>
  <name>Benzonitrile</name>
  <sample>Uvasol and analytical grade. Serlabo sample, purity 99 mole%.</sample>
 </substances>
 <substances>
  <casrn>123-91-1</casrn>
  <constituent>2</constituent>
  <formula>C4H8O2</formula>
  <inchi>InChI=1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2</inchi>
  <inchikey>RYHBNJHYFVUHQT-UHFFFAOYSA-N</inchikey>
  <molweight>88.1051</molweight>
  <name>1,4-Dioxane</name>
  <sample>Uvasol and analytical grade. Serlabo sample, purity 99 mole%.</sample>
 </substances>
 <substances>
  <casrn>98-95-3</casrn>
  <constituent>2</constituent>
  <formula>C6H5NO2   </formula>
  <inchi>InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H</inchi>
  <inchikey>LQNUZADURLCDLV-UHFFFAOYSA-N</inchikey>
  <molweight>123.109</molweight>
  <name>Nitrobenzene</name>
  <sample>Uvasol and analytical grade. Serlabo sample, purity 99 mole%.</sample>
 </substances>
 <substances>
  <casrn>67-68-5</casrn>
  <constituent>2</constituent>
  <formula>C2H6OS</formula>
  <inchi>InChI=1S/C2H6OS/c1-4(2)3/h1-2H3</inchi>
  <inchikey>IAZDPXIOMUYVGZ-UHFFFAOYSA-N</inchikey>
  <molweight>78.1334</molweight>
  <name>Dimethylsulfoxide</name>
  <sample>Uvasol and analytical grade. Serlabo sample, purity 99 mole%.</sample>
 </substances>
 <substances>
  <casrn>680-31-9</casrn>
  <constituent>2</constituent>
  <formula>C6H18N3OP</formula>
  <inchi>InChI=1S/C6H18N3OP/c1-7(2)11(10,8(3)4)9(5)6/h1-6H3</inchi>
  <inchikey>GNOIPBMMFNIUFM-UHFFFAOYSA-N</inchikey>
  <molweight>179.2</molweight>
  <name>Hexamethylphosphoric triamide</name>
  <sample>Uvasol and analytical grade. Serlabo sample, purity 99 mole%.</sample>
 </substances>
 <system>Ethene with Benzonitrile, 1,4-Dioxane, Nitrobenzene, Dimethylsulfoxide, or Hexamethylphosphoric triamide</system>
 <title>Solubility data from IUPAC SDS Volume 57 (page ?) - Ethene with Benzonitrile, 1,4-Dioxane, Nitrobenzene, Dimethylsulfoxide, or Hexamethylphosphoric triamide</title>
</compilation>