<compilation>
 <compilers>William E. Acree, Jr.</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>2.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>2.92e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.92</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.708e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.708</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>3.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>4.89e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>4.89</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.511e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.511</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>4.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>4.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>7.22e-02</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>7.22</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.278e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.278</significand>
    <unit>1</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Constant temperature bath, a precision thermometer and uv/visible spectrometer. &lt;br&gt;Mixtures of known concentrations sealed in glass ampoules and pre-equilibrated for four days at an elevated temperature. Saturated solutions were then transferred to a special solubility flask and equilibrated for three days at desired temperature. Aliquots removed, diluted ten-fold with solvent and concentrations determined spectrophotometrically at 270 nm.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>McLaughlin, E.; Scott, R. L.; J. Phys. Chem. 1954, 76, 5276-5279.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01650a004</url>
 </sources>
 <substances>
  <casrn>85-01-8</casrn>
  <constituent>1</constituent>
  <formula>C14H10</formula>
  <inchi>InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H</inchi>
  <inchikey>YNPNZTXNASCQKK-UHFFFAOYSA-N</inchikey>
  <molweight>178.229</molweight>
  <name>Phenanthrene</name>
  <sample>White Label, Eastman Kodak Company, Rochester, New York, USA, was recrystallized five times from ethanol to give a melting point of 101&amp;deg;C.</sample>
 </substances>
 <substances>
  <casrn>311-89-7</casrn>
  <constituent>2</constituent>
  <formula>C12F27N</formula>
  <inchi>InChI=1S/C12F27N/c13-1(14,7(25,26)27)4(19,20)10(34,35)40(11(36,37)5(21,22)2(15,16)8(28,29)30)12(38,39)6(23,24)3(17,18)9(31,32)33</inchi>
  <inchikey>RVZRBWKZFJCCIB-UHFFFAOYSA-N</inchikey>
  <molweight>671.092</molweight>
  <name>Heptacosafluorotributanamine</name>
  <sample>Purity not specified, Minnesota Mining &amp; Manufacturing Company, USA, was distilled shortly before use.</sample>
 </substances>
 <system>Phenanthrene with Perfluoro-tri-n-butylamine</system>
 <title>Solubility data from IUPAC SDS Volume 59 (page ?) - Phenanthrene with Perfluoro-tri-n-butylamine</title>
</compilation>