<compilation>
 <compilers>Walter Hayduk</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.9315e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>5</sigfigs>
    <significand>2.9315</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <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>
    <exponent>-3</exponent>
    <number>9.50e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.50</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>2.52e+00</number>
    <property>Ostwald coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>2.52</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <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>
   <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>-3</exponent>
    <number>8.64e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.64</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>0</exponent>
    <number>2.32e+00</number>
    <property>Ostwald coefficient</property>
    <sigfigs>3</sigfigs>
    <significand>2.32</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The solvent was held in a jacketed burette. Constant temperature water was circulated through the jacket. Gas was bubbled through the solvent until saturated. The dissolved gas content was determined by an electrometric dead-stop titration technique which yielded the bromine number. The electrometric titrator was based on a design given in [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Dubois, H. D.; Skoog, D. A.; Anal. Chem. 1948, 20, 624.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ac60019a008</url>
 </reference>
 <sources>
  <citation>Narasimhan, S.; Natarajan, G. S.; Nageshwar, G. D.; Indian J. Technol. 1981, 19, 298-299.</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>Ethene prepared by catalytic dehydration of ethanol over activated alumina at 350-400&amp;deg;C and analyzed by chromatography. Purity not given.</sample>
 </substances>
 <substances>
  <casrn>71-36-3</casrn>
  <constituent>2</constituent>
  <formula>C4H10O</formula>
  <inchi>InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3</inchi>
  <inchikey>LRHPLDYGYMQRHN-UHFFFAOYSA-N</inchikey>
  <molweight>74.1216</molweight>
  <name>1-Butanol</name>
  <sample>1-Butanol was treated for the removal of aldehydes and ketones and then distilled twice in a packed column.</sample>
 </substances>
 <system>Ethene with 1-Butanol</system>
 <title>Solubility data from IUPAC SDS Volume 57 (page ?) - Ethene with 1-Butanol</title>
</compilation>