<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <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>1.9e-03</number>
    <property>Mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>1.9</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>1</exponent>
    <number>1.228e+01</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>4</sigfigs>
    <significand>1.228</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-4</exponent>
    <number>2.36e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>2.36</significand>
    <unit>1</unit>
   </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>-4</exponent>
    <number>4.3e-04</number>
    <property>Mass fraction (1)</property>
    <sigfigs>2</sigfigs>
    <significand>4.3</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>1</exponent>
    <number>2.157e+01</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>4</sigfigs>
    <significand>2.157</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-5</exponent>
    <number>5.67e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.67</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>A 20 mL 1,2-dibromoethane sample was mixed with 40 mL aqueous electrolyte solution in a flask fitted with a thermostat jacket and a powerful stirrer. After a stirring time of 2-3 days, samples were taken from both phases for analysis. The bromine concentration was determined by adding $\ce{HNO3}$ to the solution and the free bromine was titrated with $\ce{AgNO3}$ solution. The water content of the organic rich phase was calculated by the method of Kariusu [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Shostakovskii, M. F.; Druzhinin, I. G.; Zh. Obshch. Khim. 12, 42-47 (1942).</citation>
  <pubtype>paper</pubtype>
 </reference>
 <sources>
  <citation>Druzhinin, I. G.; Shostakovskii, M. F.; J. Gen. Chem. USSR 12, 48-54 (1942).</citation>
  <pubtype>paper</pubtype>
 </sources>
 <substances>
  <casrn>7786-30-3</casrn>
  <constituent>2</constituent>
  <formula>MgCl2</formula>
  <inchi>InChI=1S/2ClH.Mg/h2*1H;/q;;+2/p-2</inchi>
  <inchikey>TWRXJAOTZQYOKJ-UHFFFAOYSA-L</inchikey>
  <molweight>95.211</molweight>
  <name>Magnesium chloride</name>
  <sample>Source and purity not given.</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>Distilled.</sample>
 </substances>
 <substances>
  <casrn>106-93-4</casrn>
  <constituent>1</constituent>
  <formula>C2H4Br2</formula>
  <inchi>InChI=1S/C2H4Br2/c3-1-2-4/h1-2H2</inchi>
  <inchikey>PAAZPARNPHGIKF-UHFFFAOYSA-N</inchikey>
  <molweight>187.861</molweight>
  <name>1,2-Dibromoethane</name>
  <sample>Source and purity not given.</sample>
 </substances>
 <system>1,2-Dibromoethane with Magnesium chloride and Water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 561) - 1,2-Dibromoethane with Magnesium chloride and Water</title>
</compilation>