<compilation>
 <compilers>Nikolai V. Sazonov, Valerii P. Sazonov</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The synthetic method was used. Determinations were made in test tubes, which were heated and allowed to cool slowly in air. Thermometers were roughly calibrated.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Comish, R. E.; Archibald, R. C.; Murphy, E. A.; Evans, H. M.; Ind. Eng. Chem. 26, 397-406 (1934).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ie50292a010</url>
 </sources>
 <substances>
  <casrn>75-05-8</casrn>
  <constituent>1</constituent>
  <formula>C2H3N</formula>
  <inchi>InChI=1S/C2H3N/c1-2-3/h1H3</inchi>
  <inchikey>WEVYAHXRMPXWCK-UHFFFAOYSA-N</inchikey>
  <molweight>41.052</molweight>
  <name>Acetonitrile</name>
  <sample>Prepared from sodium cyanide and dimethyl sulfate; the crude product was distilled and successively washed with solid sodium hydroxide and P&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5&lt;/sub&gt;; carefully fractionated in a 6.09 &lt;i&gt;m&lt;/i&gt; column; &lt;i&gt;d&lt;/i&gt;(20&amp;deg;C,4&amp;deg;C)=0.782 15.</sample>
 </substances>
 <substances>
  <casrn>142-82-5</casrn>
  <constituent>2</constituent>
  <formula>C7H16</formula>
  <inchi>InChI=1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3</inchi>
  <inchikey>IMNFDUFMRHMDMM-UHFFFAOYSA-N</inchikey>
  <molweight>100.202</molweight>
  <name>Heptane</name>
  <sample>Source not specified; commercial high-grade reagent.</sample>
 </substances>
 <system>Acetonitrile with Heptane</system>
 <title>Solubility data from IUPAC SDS Volume 78 (page ?) - Acetonitrile with Heptane</title>
</compilation>