<compilation>
 <compilers>Valerii P. Sazonov</compilers>
 <dataset>
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   <conditions>
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    <unit>$\pu{K}$</unit>
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   </supplemental>
   <supplemental>
    <exponent>-2</exponent>
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   </supplemental>
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    <unit>&amp;deg;C</unit>
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   <conditions>
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  <points>
   <conditions>
    <exponent>1</exponent>
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    <unit>&amp;deg;C</unit>
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   <conditions>
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    <unit>$\pu{K}$</unit>
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   <data>
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    <sigfigs>4</sigfigs>
    <significand>3.510</significand>
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   </data>
   <data>
    <exponent>-1</exponent>
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   </data>
   <pntnum>9</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>5.026e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
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    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>2.313e-01</number>
    <property>Mole fraction - Liquid (2)</property>
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  </points>
  <series>1</series>
  <title>Solubility temperatures of the liquid phases</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The synthetic method (Alekseev [1]) was used. Mixtures of (1), (2) and (3) of total mass 10 g were heated with vigorous stirring to a temperature higher than the homogenization temperature, then slowly cooled until turbidity appeared. Heating and cooling cycles were repeated twice. Temperature values obtained for appearing and disappearing turbidity were averaged.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Alekseev, V. F.; Zh. Russ. Fiz. -Khim. O-va 8, 249 (1876).</citation>
  <pubtype>paper</pubtype>
 </reference>
 <sources>
  <citation>Gudkina, L. V.; Ph.D. Dissertation, Novosibirsk Institute of Inorganic Chemistry, Russia, 1975.</citation>
  <pubtype>dissertation</pubtype>
 </sources>
 <substances>
  <casrn>75-52-5</casrn>
  <constituent>1</constituent>
  <formula>CH3NO2 </formula>
  <inchi>InChI=1S/CH3NO2/c1-2(3)4/h1H3</inchi>
  <inchikey>LYGJENNIWJXYER-UHFFFAOYSA-N</inchikey>
  <molweight>61.04</molweight>
  <name>Nitromethane</name>
  <sample>Source not specified; pure grade reagent; dried and twice distilled in a glass packed column.</sample>
 </substances>
 <substances>
  <casrn>74-95-3</casrn>
  <constituent>2</constituent>
  <formula>CH2Br2</formula>
  <inchi>InChI=1S/CH2Br2/c2-1-3/h1H2</inchi>
  <inchikey>FJBFPHVGVWTDIP-UHFFFAOYSA-N</inchikey>
  <molweight>173.835</molweight>
  <name>Dibromomethane</name>
  <sample>Source not specified; pure grade reagent; dried and twice distilled in a glass packed column.</sample>
 </substances>
 <substances>
  <casrn>107-21-1</casrn>
  <constituent>3</constituent>
  <formula>C2H6O2 </formula>
  <inchi>InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2</inchi>
  <inchikey>LYCAIKOWRPUZTN-UHFFFAOYSA-N</inchikey>
  <molweight>62.0678</molweight>
  <name>1,2-Ethanediol</name>
  <sample>Analytical purity; dried and twice distilled under vacuum; 0.03 mass% water by the Karl Fischer analysis.</sample>
 </substances>
 <system>Nitromethane with Dibromomethane and 1,2-Ethanediol</system>
 <title>Solubility data from IUPAC SDS Volume 72 (page 1532) - Nitromethane with Dibromomethane and 1,2-Ethanediol</title>
</compilation>