<compilation>
 <compilers>William E. Acree, Jr.</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.062e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.062</significand>
    <unit>K</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>5.02e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.02</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.498e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.498</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.198e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.198</significand>
    <unit>K</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>9.10e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.10</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.090e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.090</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.318e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.318</significand>
    <unit>K</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>1.515e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.515</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>8.485e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>8.485</significand>
    <unit>1</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.422e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.422</significand>
    <unit>K</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>2.435e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>2.435</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>7.565e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>7.565</significand>
    <unit>1</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Constant temperature bath and a precision thermometer. &lt;br&gt;Mixtures of known concentrations sealed in glass ampoules and placed in constant temperature to equilibrate. Samples were rotated while bath temperature slowly increased. Solubility determined by visual noting the same temperature at which the last trace of solid solute disappeared.*</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>McLaughlin, E.; Zainal, H. A.; J. Chem. Soc. 1960, 2485-2488.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1039/jr9600002485</url>
 </sources>
 <substances>
  <casrn>86-73-7</casrn>
  <constituent>1</constituent>
  <formula>C13H10</formula>
  <inchi>InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2</inchi>
  <inchikey>NIHNNTQXNPWCJQ-UHFFFAOYSA-N</inchikey>
  <molweight>166.219</molweight>
  <name>Fluorene</name>
  <sample>Purity not given, Gesellschaft fur Teerverwertung, was passed over an alumina column with benzene as eluant.</sample>
 </substances>
 <substances>
  <casrn>110-82-7</casrn>
  <constituent>2</constituent>
  <formula>C6H12</formula>
  <inchi>InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2</inchi>
  <inchikey>XDTMQSROBMDMFD-UHFFFAOYSA-N</inchikey>
  <molweight>84.1595</molweight>
  <name>Cyclohexane</name>
  <sample>Purity, source and purification method was not specified.</sample>
 </substances>
 <system>Fluorene with Cyclohexane</system>
 <title>Solubility data from IUPAC SDS Volume 59 (page 34) - Fluorene with Cyclohexane</title>
</compilation>