<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>3.7e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>3.7</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <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>7.8e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>7.8</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <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>-1</exponent>
    <number>1.20e-01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.20</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <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>-1</exponent>
    <number>1.95e-01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>1.95</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>4</pntnum>
   <supplemental></supplemental>
  </points>
  <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>-1</exponent>
    <number>3.3e-01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>3.3</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>5</pntnum>
   <supplemental></supplemental>
  </points>
  <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>-1</exponent>
    <number>9.2e-01</number>
    <property>Amount concentration (1)</property>
    <sigfigs>2</sigfigs>
    <significand>9.2</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>6</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Constant temperature bath, and an ultraviolet/visible spectrophotometer. Excess solute and binary solvent equilibrated in a constant temperature vessel. Aliquots of saturated solution withdrawn and concentrations determined spectrometrically at 283 nm. Attainment of equilibrium verified by several repetitive measurements.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Burgess, J.; Haines, R. I.; Chem. Ind. (London) 1980, 289.</citation>
  <pubtype>paper</pubtype>
 </sources>
 <substances>
  <casrn>366-18-7</casrn>
  <constituent>1</constituent>
  <formula>C10H8N2</formula>
  <inchi>InChI=1S/C10H8N2/c1-3-7-11-9(5-1)10-6-2-4-8-12-10/h1-8H</inchi>
  <inchikey>ROFVEXUMMXZLPA-UHFFFAOYSA-N</inchikey>
  <molweight>156.184</molweight>
  <name>2,2-Bipyridine</name>
  <sample>Purity and chemical source not specified, was recrystallized from aqueousethanol.</sample>
 </substances>
 <substances>
  <casrn>75-65-0</casrn>
  <constituent>2</constituent>
  <formula>C4H10O</formula>
  <inchi>InChI=1S/C4H10O/c1-4(2,3)5/h5H,1-3H3</inchi>
  <inchikey>DKGAVHZHDRPRBM-UHFFFAOYSA-N</inchikey>
  <molweight>74.1216</molweight>
  <name>2-Methyl-2-propanol</name>
  <sample>Purity and chemical source not specified in paper.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>3</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Purity and chemical source not specified in paper.</sample>
 </substances>
 <system>2,2'-Bipyridine with 2-Methyl-2-propanol and Water</system>
 <title>Solubility data from IUPAC SDS Volume 58 (page 205) - 2,2'-Bipyridine with 2-Methyl-2-propanol and Water</title>
</compilation>