<compilation>
 <compilers>Valerii P. Sazonov</compilers>
 <dataset>
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    <unit>&amp;deg;C</unit>
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    <property>Ambient temperature</property>
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    <exponent>-2</exponent>
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   <conditions>
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    <exponent>1</exponent>
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   <supplemental>
    <exponent>-1</exponent>
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   <conditions>
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    <property>Ambient temperature</property>
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    <unit>&amp;deg;C</unit>
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   <conditions>
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    <unit>K</unit>
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   <pntnum>11</pntnum>
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    <exponent>-1</exponent>
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    <unit>1</unit>
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   <supplemental>
    <exponent>-2</exponent>
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    <property>Mole fraction - Liquid (2)</property>
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  <points>
   <conditions>
    <exponent>1</exponent>
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    <property>Ambient temperature</property>
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    <unit>&amp;deg;C</unit>
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   <conditions>
    <exponent>2</exponent>
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    <property>Ambient temperature</property>
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    <unit>K</unit>
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    <property>Mass fraction (1)</property>
    <sigfigs>3</sigfigs>
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    <unit>1</unit>
   </data>
   <data>
    <exponent>-2</exponent>
    <number>5.5e-02</number>
    <property>Mass fraction (2)</property>
    <sigfigs>2</sigfigs>
    <significand>5.5</significand>
    <unit>1</unit>
   </data>
   <pntnum>12</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>8.86e-01</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
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    <unit>1</unit>
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   <supplemental>
    <exponent>-2</exponent>
    <number>4.5e-02</number>
    <property>Mole fraction - Liquid (2)</property>
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    <unit>1</unit>
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  </points>
  <series>1</series>
  <title>Mutual solubility of nitromethane, benzene and cyclohexane</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The titration method, as described in Dunnery and Atwood,&lt;sup&gt;2&lt;/sup&gt; was used. Solutions and solvents were thermally equilibrated and held at constant temperature during titrations. Enough solution was taken to give a titer of 10 to 20 mL.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Dunnery, D. A.; Atwood, G. R.; Talanta 15, 855 (1968).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0039-9140(68)80181-x</url>
 </reference>
 <sources>
  <citation>Suri, S. K.; Talanta 17, 577 (1970).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0039-9140(70)80005-4</url>
 </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; purified by methods as in Weissberger&lt;sup&gt;1&lt;/sup&gt;; &amp;rho;(30&amp;deg;C) = 1125.0 g  L&lt;sup&gt;-1&lt;/sup&gt;,&amp;rho;(40&amp;deg;C) = 1110.8 g &amp;middot; L&lt;sup&gt;-1&lt;/sup&gt;.</sample>
 </substances>
 <substances>
  <casrn>71-43-2</casrn>
  <constituent>2</constituent>
  <formula>C6H6</formula>
  <inchi>InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H</inchi>
  <inchikey>UHOVQNZJYSORNB-UHFFFAOYSA-N</inchikey>
  <molweight>78.1118</molweight>
  <name>Benzene</name>
  <sample>Source not specified; purified by methods as in Weissberger&lt;sup&gt;1&lt;/sup&gt;; &amp;rho;(30&amp;deg;C) = 868.5 g L&lt;sup&gt;-1&lt;/sup&gt;, &amp;rho;(40&amp;deg;C) = 857.5 g&amp;middot;L&lt;sup&gt;-1&lt;/sup&gt;.</sample>
 </substances>
 <substances>
  <casrn>110-82-7</casrn>
  <constituent>3</constituent>
  <formula>C6H12</formula>
  <inchi>InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2</inchi>
  <inchikey>XDTMQSROBMDMFD-UHFFFAOYSA-N</inchikey>
  <molweight>84.1595</molweight>
  <name>Cyclohexane</name>
  <sample>Source not specified; purified by methods as in Weissberger&lt;sup&gt;1&lt;/sup&gt;; &amp;rho;(30&amp;deg;C) = 769.4 g L&lt;sup&gt;-1&lt;/sup&gt;.&amp;rho;(40&amp;deg;C) = 759.6 g&amp;middot;L&lt;sup&gt;-1&lt;/sup&gt; .</sample>
 </substances>
 <system>Nitromethane with Benzene and Cyclohexane</system>
 <title>Solubility data from IUPAC SDS Volume 72 (page ?) - Nitromethane with Benzene and Cyclohexane</title>
</compilation>