<compilation>
 <compilers>William E. Acree, Jr.</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.730e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.730</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>1.272e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.272</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>8.728e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>8.728</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>2.844e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>2.844</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>1.654e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.654</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>8.346e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>8.346</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.259e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.259</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>4.219e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>4.219</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>5.783e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>5.783</significand>
    <unit>1</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Experimental procedure only marginally described by author. Excess solute and solvent were equilibrated in a constant temperature water bath for between 10-30 minutes. Saturated solution was withdrawn through a coarse filter and analyzed by specific gravity. Author noted that evaporation to dryness and weighing the residue was subject to too much decomposition.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Speyers, C. L.; Am. J. Sci. 1902, 14, 293-302.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.2475/ajs.s4-14.82.293</url>
 </sources>
 <substances>
  <casrn>83-32-9</casrn>
  <constituent>1</constituent>
  <formula>C12H10</formula>
  <inchi>InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2</inchi>
  <inchikey>CWRYPZZKDGJXCA-UHFFFAOYSA-N</inchikey>
  <molweight>154.208</molweight>
  <name>Acenaphthene</name>
  <sample>Purity not given, Kahlbaum, was recrystallized from alcohol to a melting point temperature of 93.5&amp;deg;C.</sample>
 </substances>
 <substances>
  <casrn>67-66-3</casrn>
  <constituent>2</constituent>
  <formula>CHCl3</formula>
  <inchi>InChI=1S/CHCl3/c2-1(3)4/h1H</inchi>
  <inchikey>HEDRZPFGACZZDS-UHFFFAOYSA-N</inchikey>
  <molweight>119.378</molweight>
  <name>Trichloromethane</name>
  <sample>Purity unknown, several sources listed, washed with water, sulfuric acid, dried over calcium chloride and distilled.</sample>
 </substances>
 <system>Acenaphthene with Trichloromethane</system>
 <title>Solubility data from IUPAC SDS Volume 58 (page 17) - Acenaphthene with Trichloromethane</title>
</compilation>