<compilation>
 <compilers>Marie C. Haulait-Pirson</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>(1) was saturated by storing over a layer of (2) in a brown glass bottle without any agitation. The bottle was sealed with serum cap and completely submerged in the water-bath for seven days. A 20 mL sample was withdrawn with a silicone-hydrophobized hypodermic syringe. Stabilized Karl Fischer reagent diluted to a titer of 1.0-1.3 mg (2)/mL was used to titrate (2) in (1) directly in the presence of methanol to a 'dead-stop' end-point using a Beckman KF3 automatic titrimeter.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Schatzberg, P.; J. Phys. Chem. 1963, 67, 776-9.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100798a014</url>
 </sources>
 <substances>
  <casrn>142-82-5</casrn>
  <constituent>1</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>Eastman Organic Chemicals; doubly distilled; passed repeatedly through a column of silica gel until no absorption occurred in the 220 to 340 nm spectral range.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>2</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Distilled and deionized.</sample>
 </substances>
 <system>Heptane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 37 (page 498) - Heptane with Water</title>
</compilation>