<compilation>
 <compilers>Marie C. Haulait-Pirson</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.7e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.7</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.7e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.7</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.7e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.7</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
  <title>Solubility of triphenylene in water</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The method consisted of preparing serial dilutions of a suspension of [1] in [2] and determining nephelometrically the amount of [1] per unit volume beyond which further dilution caused no reduction in light scattering, which remained equal to that of pure [2]. A Bausch and Lomb Dubosque colorimeter model 100-mm was employed. Many details are reported in [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Davis, W. W.; Krahl, M. E.; Cloves, G. H. A., J. Am. Chem. Soc. 1940, 62, 3086.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01868a054</url>
 </reference>
 <sources>
  <citation>Davis, W. W.; Krahl, M. E.; Cloves, G. H. A.; J. Am. Chem. Soc. 1942, 64, 108-10.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01253a028</url>
 </sources>
 <substances>
  <casrn>217-59-4</casrn>
  <constituent>1</constituent>
  <formula>C18H12</formula>
  <inchi>InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H</inchi>
  <inchikey>SLGBZMMZGDRARJ-UHFFFAOYSA-N</inchikey>
  <molweight>228.288</molweight>
  <name>Triphenylene</name>
  <sample>Prepared at Harvard University; MP = 197.5-197.9&amp;deg;C (cf. [2]).</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>Dust-free.</sample>
 </substances>
 <system>Triphenylene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 38 (page ?) - Triphenylene with Water</title>
</compilation>