<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>3.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>3.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-4</exponent>
    <number>6.08e-04</number>
    <property>Relative mass - solution (1)</property>
    <sigfigs>3</sigfigs>
    <significand>6.08</significand>
    <unit>g&lt;sub&gt;1&lt;/sub&gt;/g&lt;sub&gt;2&lt;/sub&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>6.08e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>6.08</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>8.00e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.00</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>An excess of 1-bromobutane in 500 g water was shaken for 12 hours in a waterbath thermostat. Samples were then withdrawn and read against pure water in an interferometer made by Zeiss [1]. A detailed description of the complete procedure is given in a Ph.D. thesis [2].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Saylor, J. H.; Ph.D. Dissertation, Duke University, Durham, NC, 1930.</citation>
  <pubtype>dissertation</pubtype>
 </reference>
 <sources>
  <citation>Gross, P. M.; Saylor, J. H.; J. Am. Chem. Soc. 1931, 53, 1744-51.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01356a016</url>
 </sources>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>2</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>distilled.</sample>
 </substances>
 <substances>
  <casrn>109-65-9</casrn>
  <constituent>1</constituent>
  <formula>C4H9Br</formula>
  <inchi>InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3</inchi>
  <inchikey>MPPPKRYCTPRNTB-UHFFFAOYSA-N</inchikey>
  <molweight>137.018</molweight>
  <name>1-Bromobutane</name>
  <sample>Eastman Kodak Company. Purified by fractional distillation before use.</sample>
 </substances>
 <system>1-Bromobutane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 68 (page ?) - 1-Bromobutane with Water</title>
</compilation>