<compilation>
 <compilers>Marie C. Haulait-Pirson</compilers>
 <dataset></dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A saturated solution of (1) in (2) was vigorously stirred in a 250 mL flask for 24 hrs. and subsequently settled at 25 °C for at least 48 hrs. Then the saturated solution was decanted and filtered and 50-100 mL extracted with approximately 5 mL of cyclohexane in a separatory funnel. After shaking for 2 hrs. the cyclohexane extract was removed for analysis. An Aminco-Browman spectrophotofluorometer (American Instruments Ltd.) was used for analysis. Many details are given in the paper.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Mackay, D.; Shiu, W. Y.; J. Chem. Eng. Data. 1977, 22, 399-402.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/je60075a012</url>
 </sources>
 <substances>
  <casrn>56-49-5</casrn>
  <constituent>1</constituent>
  <formula>C21H16</formula>
  <inchi>InChI=1S/C21H16/c1-13-6-7-15-12-20-17-5-3-2-4-14(17)8-9-18(20)19-11-10-16(13)21(15)19/h2-9,12H,10-11H2,1H3</inchi>
  <inchikey>PPQNQXQZIWHJRB-UHFFFAOYSA-N</inchikey>
  <molweight>268.352</molweight>
  <name>3-Methylcholantrene</name>
  <sample>Aldrich Chemicals, Eastman Kodak, or K and K Laboratories, commercial highest grade; used as received.</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>doubly distilled.</sample>
 </substances>
 <system>3-Methylcholantrene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 38 (page ?) - 3-Methylcholantrene with Water</title>
</compilation>