<compilation>
 <compilers>Valerii P. Sazonov</compilers>
 <dataset>
  <points>
   <conditions></conditions>
   <data>
    <exponent>1</exponent>
    <number>9.30e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>9.30</significand>
    <unit>&amp;deg;C</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>2</exponent>
    <number>3.662e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.662</significand>
    <unit>$\pu{K}$</unit>
   </supplemental>
  </points>
  <series>1</series>
  <title>Upper critical solution temperatures of the systems nitromethane (1) + 1-Nonadecanol (2)</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The synthetic method was used. A Reichert microscope, type RCH, equipped with a heating stage was used as described in Schmid, et al. [1]. The disappearance and reappearance of the interface between (1) and (2) could be observed without difficulty.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; J. Am. Oil Chem. Soc. 42, 372 (1965).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1007/bf02635572</url>
 </reference>
 <sources>
  <citation>Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; Microchem. J. 9, 134-144 (1965).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1016/0026-265x(65)90094-9</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>Fisher Scientific Co.; certified, No. N-98;&lt;br/&gt;$n_{D}^{20}$ = \pu{1.3820}$, $\rho^{20} = \pu{1134 g L-1}$.</sample>
 </substances>
 <substances>
  <constituent>2</constituent>
  <formula>C19H40O</formula>
  <molweight>284.5</molweight>
  <name>1-Nonadecanol</name>
  <sample>Some alcohols obtained from the Hormel Institute and from Lachat Chemicals; all other alcohols prepared by reduction of the corresponding methyl esters with lithium aluminum hydride; purified by gas-liquid partition chromatography.</sample>
 </substances>
 <system>Nitromethane with 1-Nonadecanol</system>
 <title>Solubility data from IUPAC SDS Volume 71 (page 11298) - Nitromethane with 1-Nonadecanol</title>
</compilation>