<compilation>
 <compilers>Valerii P. Sazonov</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>
   <conditions>
    <exponent>2</exponent>
    <number>3.03e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.03</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data>
    <exponent>0</exponent>
    <number>2.1e+00</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>2</sigfigs>
    <significand>2.1</significand>
    <unit>g&lt;sub&gt;2&lt;/sub&gt;/100 g&lt;sub&gt;1&lt;/sub&gt;</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>0</exponent>
    <number>2.0e+00</number>
    <property>Percent mass fraction (2)</property>
    <sigfigs>2</sigfigs>
    <significand>2.0</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
  <title>Solubility of polymers in nitromethanenitromethane (1) + Poly(vinyl chloride-vinyl acetate) (Vinylite) (2)</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The method described in Marvel, et al. [1]. was used. The solubility determinations were made by adding an excess of the polymer to the solvent in a glass-stoppered bottle. The stoppered bottle was placed in a rotating device in a thermostat at 30 °C for 48 h. The saturated solution was removed weighed, evaporated and the residue weighed. This method worked well in cases where the solubility was low. In other cases, a weighed amount of solvent was added to a weighed sample of polymer. The mixture was shaken and allowed to stand at 25 °C for 48 h to see whether it became homogeneous. It was impossible to make accurate measurements even by this procedure. Hence the values given in the table for these high solubilities are to be regarded as minimum values.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Marvel, C. S.; Dietz, F. C.; Copley, M. J.; J. Am. Chem. Soc. 62, 2273 (1940).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01866a006</url>
 </reference>
 <sources>
  <citation>Marvel, C. S.; Harkema, J.; Copley, M. J.; J. Am. Chem. Soc,. 63, 1609 (1941).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01851a033</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; laboratory sample; redistilled and collected over a 2&amp;deg;C boiling range.</sample>
 </substances>
 <substances>
  <constituent>2</constituent>
  <formula>None</formula>
  <molweight>148.59</molweight>
  <name>Poly(vinyl chloride-vinyl acetate) (Vinylite)</name>
  <sample>Some polymers (*) obtained from Carbide and Carbon Chemicals Corp.; others from du Pont Co.; technical grade.</sample>
 </substances>
 <system>Nitromethane with Poly(vinyl chloride-vinyl acetate) (Vinylite)</system>
 <title>Solubility data from IUPAC SDS Volume 71 (page 1337) - Nitromethane with Poly(vinyl chloride-vinyl acetate) (Vinylite)</title>
</compilation>