<compilation>
 <compilers>William E. Acree, Jr.</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.2e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.2</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-4</exponent>
    <number>9.1e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>2</sigfigs>
    <significand>9.1</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>High performance liquid chromatograph system equipped with an ultraviolet detector and integrator. Excess solute and solvent placed in 1-dram glass bottle and allowed to equilibrate for 24 hours at ambient room temperature with agitation. Saturated solution was filtered through a 0.45 micrometer poly-(tetrafluoroethylene) filter. Concentrations determined via HPLC with uv detection at 340 nm. Stationary phase was a dinitroanilinopropyl column, and a binary toluene/hexane (20:80 by volume) mobile phase was used.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Ruoff, R. S.; Tse, D. S.; Malhotra, R.; Lorents, D. C.; J. Phys. Chem. 1993, 97, 3379-3383.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100115a049</url>
 </sources>
 <substances>
  <casrn>99685-96-8</casrn>
  <constituent>1</constituent>
  <formula>C60</formula>
  <inchi>InChI=1S/C60/c1-2-5-6-3(1)8-12-10-4(1)9-11-7(2)17-21-13(5)23-24-14(6)22-18(8)28-20(12)30-26-16(10)15(9)25-29-19(11)27(17)37-41-31(21)33(23)43-44-34(24)32(22)42-38(28)48-40(30)46-36(26)35(25)45-39(29)47(37)55-49(41)51(43)57-52(44)50(42)56(48)59-54(46)53(45)58(55)60(57)59</inchi>
  <inchikey>XMWRBQBLMFGWIX-UHFFFAOYSA-N</inchikey>
  <molweight>720.642</molweight>
  <name>Buckminsterfullerene</name>
  <sample>Graphite soot obtained by passing an ac discharge between spectroscopic grade graphite, and sample purified by chromatographic separation on alumina column. Final purity of 99.95% as determined by mass spectrometry.</sample>
 </substances>
 <substances>
  <casrn>554-14-3</casrn>
  <constituent>2</constituent>
  <formula>C5H6S</formula>
  <inchi>InChI=1S/C5H6S/c1-5-3-2-4-6-5/h2-4H,1H3</inchi>
  <inchikey>XQQBUAPQHNYYRS-UHFFFAOYSA-N</inchikey>
  <molweight>98.1661</molweight>
  <name>2-methylthiophene</name>
  <sample>Reagent grade, 99% (or better), chemical source not given, used as received from manufacturer.</sample>
 </substances>
 <system>Buckminsterfullerene with 2-Methylthiophene</system>
 <title>Solubility data from IUPAC SDS Volume 58 (page 241) - Buckminsterfullerene with 2-Methylthiophene</title>
</compilation>