<compilation>
 <compilers>Valerii P. Sazonov</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>5.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>5.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.282e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.282</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>5.65e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>5.65</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.297e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.297</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.10e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>6.10</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.342e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.342</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>3</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.40e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>6.40</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.372e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.372</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>4</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>6.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.382e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.382</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>5</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.80e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>6.80</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.412e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.412</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>6</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>6.85e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>6.85</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.417e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.417</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>7</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.10e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.10</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.442e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.442</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>8</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.15e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.15</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.447e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.447</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>9</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.35e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.35</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.467e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.467</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>10</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.40e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.40</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.472e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.472</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>11</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.482e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.482</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>12</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>7.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>7.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>2</exponent>
    <number>3.482e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.482</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <data></data>
   <pntnum>13</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
  <title>Upper critical solution temperatures of the binary systems acetonitrile (1) + ester (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 elsewhere [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>75-05-8</casrn>
  <constituent>1</constituent>
  <formula>C2H3N</formula>
  <inchi>InChI=1S/C2H3N/c1-2-3/h1H3</inchi>
  <inchikey>WEVYAHXRMPXWCK-UHFFFAOYSA-N</inchikey>
  <molweight>41.052</molweight>
  <name>Acetonitrile</name>
  <sample>Baker Chemical Co.; reagent No. 9011; $n_{D}^{20}$ = 1.3445, $d_{4}^{20}$ = 0.780.</sample>
 </substances>
 <substances>
  <casrn>111-61-5</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>MVLVMROFTAUDAG-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Ethyl octadecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>66455-49-0</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20-21/h20H,2-19H2,1H3</inchi>
  <inchikey>HNKCZZOHAXMGMR-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Nonadecyl formate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>822-23-1</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h3-19H2,1-2H3</inchi>
  <inchikey>OIZXRZCQJDXPFO-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Octadecyl acetate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>1731-94-8</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-2/h3-19H2,1-2H3</inchi>
  <inchikey>BDXAHSJUDUZLDU-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Methyl nonadecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>66455-48-9</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(21)4-2/h3-19H2,1-2H3</inchi>
  <inchikey>CHQQYYTVIJYGOS-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Heptadecyl propanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>6221-99-4</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-20(21)18-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>NJVKAQGGBANCKG-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Hexadecyl butanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>26718-84-3</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20(21)22-19-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>SXTULBAGGXUEQH-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Propyl heptadecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>111-06-8</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-20(21)22-19-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>GLYJVQDYLFAUFC-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Butyl hexadecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>71801-23-5</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-8-9-10-11-12-13-14-15-17-19-22-20(21)18-16-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>SMMNCBBCUVMKHP-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Tetradecyl hexanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>20292-09-5</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-9-10-11-12-13-15-17-19-22-20(21)18-16-14-8-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>OYQTUTLMOLEYNR-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Dodecyl octanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>42231-99-2</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-9-10-11-12-13-14-15-16-18-20(21)22-19-17-8-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>JIFCVUWJQMDNTN-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Hexyl tetradecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>5303-24-2</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-9-11-12-13-14-16-18-20(21)22-19-17-15-10-8-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>BBZAGOMQOSEWBH-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Octyl dodecanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <substances>
  <casrn>1654-86-0</casrn>
  <constituent>2</constituent>
  <formula>C20H40O2</formula>
  <inchi>InChI=1S/C20H40O2/c1-3-5-7-9-11-13-15-17-19-22-20(21)18-16-14-12-10-8-6-4-2/h3-19H2,1-2H3</inchi>
  <inchikey>XAKXZZPEUKNHMA-UHFFFAOYSA-N</inchikey>
  <molweight>312.53</molweight>
  <name>Decyl decanoate</name>
  <sample>Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, acetate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.</sample>
 </substances>
 <system>Acetonitrile with Esters (C20)</system>
 <title>Solubility data from IUPAC SDS Volume 78 (page ?) - Acetonitrile with Esters (C20)</title>
</compilation>