<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>-3</exponent>
    <number>2.57e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.57</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.974e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.974</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>-3</exponent>
    <number>4.02e-03</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>4.02</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>9.960e-01</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>4</sigfigs>
    <significand>9.960</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</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 placed in special solubility flask and equilibrated in a constant temperature bath for 48 hours. The entire saturated solution was withdrawn by suction. Solubility based upon weight of undissolved solid, which remained in the solubility flask after solution was removed.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Simons, J. H.; Linevsky, M. J.; J. Am. Chem. Soc. 1952, 74, 4750-4751.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01139a007</url>
 </sources>
 <substances>
  <casrn>91-20-3</casrn>
  <constituent>1</constituent>
  <formula>C10H8</formula>
  <inchi>InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H</inchi>
  <inchikey>UFWIBTONFRDIAS-UHFFFAOYSA-N</inchikey>
  <molweight>128.171</molweight>
  <name>Naphthalene</name>
  <sample>Purity and source not given, was recrystallized two times from ethanol.</sample>
 </substances>
 <substances>
  <casrn>308-48-5</casrn>
  <constituent>2</constituent>
  <formula>C8F18O</formula>
  <inchi>InChI=1S/C8F18O/c9-1(10,5(17,18)19)3(13,14)7(23,24)27-8(25,26)4(15,16)2(11,12)6(20,21)22</inchi>
  <inchikey>LOJJTTDNNWYSGX-UHFFFAOYSA-N</inchikey>
  <molweight>454.056</molweight>
  <name>Perfluoro-dibutyl ether</name>
  <sample>Purity and specific isomer not specified by authors and distilled shortly before use.</sample>
 </substances>
 <system>Naphthalene with Perfluoro-dibutyl ether</system>
 <title>Solubility data from IUPAC SDS Volume 59 (page ?) - Naphthalene with Perfluoro-dibutyl ether</title>
</compilation>