<compilation>
 <compilers>Pirketta Scharlin</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.112e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.112</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <conditions>
    <exponent>1</exponent>
    <number>3.80e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.80</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>-1</exponent>
    <number>3.00e-01</number>
    <property>Amount concentration (2)</property>
    <sigfigs>3</sigfigs>
    <significand>3.00</significand>
    <unit>mol/L</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>5.211e-01</number>
    <property>Bunsen Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>5.211</significand>
    <unit>$\pu{cm3(g) cm-3(l) atm-1}$</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>5.328e-01</number>
    <property>Solubility coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>5.328</significand>
    <unit>1</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>2</exponent>
    <number>3.112e+02</number>
    <property>Ambient temperature</property>
    <sigfigs>4</sigfigs>
    <significand>3.112</significand>
    <unit>$\pu{K}$</unit>
   </conditions>
   <conditions>
    <exponent>1</exponent>
    <number>3.80e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>3.80</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <conditions>
    <exponent>-1</exponent>
    <number>6.00e-01</number>
    <property>Amount concentration (2)</property>
    <sigfigs>3</sigfigs>
    <significand>6.00</significand>
    <unit>mol/L</unit>
   </conditions>
   <data>
    <exponent>-1</exponent>
    <number>4.969e-01</number>
    <property>Bunsen Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>4.969</significand>
    <unit>$\pu{cm3(g) cm-3(l) atm-1}$</unit>
   </data>
   <data>
    <exponent>-1</exponent>
    <number>1.340e-01</number>
    <property>Solubility coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>1.340</significand>
    <unit>1</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Solutions were saturated with $\ce{CO2}$ by a bubbling method:&lt;br/&gt;Saturation by bubbling. The solution was placed in the saturating tube, the lower end of which was connected through a wash bottle with a Kipp $\ce{CO2}$ generator. The tube and the wash bottle were immersed in a constant temperature bath. $\ce{CO2}$ was bubbled through it rapidly for 30 minutes. The wash bottle was replaced by a mercury reservoir and the free gas was driven completely out of the saturating tube by admitting mercury underneath the solution. The $\ce{CO2}$ contents of the solutions were determined in the manometric gas apparatus (Refs 1 and 2).</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Van Slyke, D. D.; Sendroy Jr., J.; J. Biol. Chem. 1927, 73, 127.</citation>
  <pubtype>paper</pubtype>
  <url>http://www.jbc.org/content/73/1/127.short.pdf+html</url>
 </reference>
 <sources>
  <citation>Van Slyke, D. D.; Sendroy Jr., J.; Hastings, A. B.; Neill, J. M.; J. Biol. Chem. 1928, 78, 765-99.</citation>
  <pubtype>paper</pubtype>
  <url>http://www.jbc.org/content/78/3/765.full.pdf+html</url>
 </sources>
 <substances>
  <casrn>124-38-9</casrn>
  <constituent>1</constituent>
  <formula>CO2</formula>
  <inchi>InChI=1S/CO2/c2-1-3</inchi>
  <inchikey>CURLTUGMZLYLDI-UHFFFAOYSA-N</inchikey>
  <molweight>44.0095</molweight>
  <name>Carbon dioxide</name>
  <sample>From a Kipp $\ce{CO2}$ generator.</sample>
 </substances>
 <substances>
  <casrn>127-95-7</casrn>
  <constituent>2</constituent>
  <formula>C2HO4K</formula>
  <inchi>InChI=1S/C2H2O4.K/c3-1(4)2(5)6;/h(H,3,4)(H,5,6);/q;+1/p-1</inchi>
  <inchikey>JMTCDHVHZSGGJA-UHFFFAOYSA-M</inchikey>
  <molweight>128.125</molweight>
  <name>Potassium hydrogen oxalate</name>
  <sample>The $\ce{KHC2O4}$ solutions were prepared from $\ce{K2C2O4}$ plus equimolar amounts of free oxalic acid crystals.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>3</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Distilled.</sample>
 </substances>
 <system>Carbon dioxide with Potassium hydrogen oxalate and Water</system>
 <title>Solubility data from IUPAC SDS Volume 62 (page ?) - Carbon dioxide with Potassium hydrogen oxalate and Water</title>
</compilation>