<compilation>
 <compilers>Marie C. Haulait-Pirson</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-4</exponent>
    <number>6.1e-04</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>2</sigfigs>
    <significand>6.1</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>1</exponent>
    <number>6e+01</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>1</sigfigs>
    <significand>6</significand>
    <unit>mg/kg</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental></supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>4.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>4.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>-3</exponent>
    <number>1.26e-03</number>
    <property>Mole fraction - Liquid (2)</property>
    <sigfigs>3</sigfigs>
    <significand>1.26</significand>
    <unit>1</unit>
   </data>
   <data>
    <exponent>2</exponent>
    <number>1.23e+02</number>
    <property>Relative mass - solution (2)</property>
    <sigfigs>3</sigfigs>
    <significand>1.23</significand>
    <unit>mg/kg</unit>
   </data>
   <pntnum>2</pntnum>
   <supplemental></supplemental>
  </points>
  <series>1</series>
  <title>Solubility of water in tridecane</title>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>(1) was saturated by storing over a layer of (2) in a brown glass bottle without any agitation. The bottle was sealed with serum cap and completely submerged in the water-bath for seven days. A 20-mL sample was withdrawn with a silicone-hydrophobized hypodermic syringe. Stabilized Karl Fischer reagent diluted to a titer of 1.0-1.3 mg (2)/mL was used to titrate (2) in (1) directly in the presence of methanol to a 'dead-stop' end-point using a Beckman KF3 automatic titrimeter.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <sources>
  <citation>Schatzberg, P.; J. Phys. Chem. 1963, 67, 776-9.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/j100798a014</url>
 </sources>
 <substances>
  <casrn>629-50-5</casrn>
  <constituent>1</constituent>
  <formula>C13H28</formula>
  <inchi>InChI=1S/C13H28/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3-13H2,1-2H3</inchi>
  <inchikey>IIYFAKIEWZDVMP-UHFFFAOYSA-N</inchikey>
  <molweight>184.361</molweight>
  <name>Tridecane</name>
  <sample>Phillips Petroleum Co.; research grade; 99.73 mole%; passed repeatedly through a column of silica gel until no absorption occurred in the 220 to 340 nm spectral range.</sample>
 </substances>
 <substances>
  <casrn>7732-18-5</casrn>
  <constituent>2</constituent>
  <formula>H2O</formula>
  <inchi>InChI=1S/H2O/h1H2</inchi>
  <inchikey>XLYOFNOQVPJJNP-UHFFFAOYSA-N</inchikey>
  <molweight>18.0153</molweight>
  <name>Water</name>
  <sample>Distilled and deionized.</sample>
 </substances>
 <system>Tridecane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 38 (page ?) - Tridecane with Water</title>
</compilation>