<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-2</exponent>
    <number>3.17e-02</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>3.17</significand>
    <unit>mol/dm&lt;sup&gt;3&lt;/sup&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>3.82e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>3.82</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>5.71e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.71</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The modified generator column method was used. A chromatographic column was coated with liquid 3-bromo-1-propene. An aqueous phase was generated by pumping water through the coated generator column. The aqueous solution was analyzed by a high pressure liquid chromatographic procedure, which has been described elsewhere [1]. The result is an average of at least three measurements.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>DeVoe, H.; Miller, M. M.; Wasik, S. P.; J. Res. Natl. Bur. Stan. 86, 361 (1981).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.6028/jres.086.015</url>
 </reference>
 <sources>
  <citation>Tewari, Y. B.; Miller, M. M.; Wasik, S. P.; Martire, D. E.; J. Chem. Eng. Data 1982, 27, 451-4.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/je00030a025</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>Baker-analysed HPLC grade.</sample>
 </substances>
 <substances>
  <casrn>106-95-6</casrn>
  <constituent>1</constituent>
  <formula>C3H5Br</formula>
  <inchi>InChI=1S/C3H5Br/c1-2-3-4/h2H,1,3H2</inchi>
  <inchikey>BHELZAPQIKSEDF-UHFFFAOYSA-N</inchikey>
  <molweight>120.976</molweight>
  <name>3-Bromo-1-propene</name>
  <sample>Source not given. At least 99% pure by GC analysis.</sample>
 </substances>
 <system>3-Bromo-1-propene with Water</system>
 <title>Solubility data from IUPAC SDS Volume 68 (page ?) - 3-Bromo-1-propene with Water</title>
</compilation>