<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>0</exponent>
    <number>5e+00</number>
    <property>Ambient temperature</property>
    <sigfigs>1</sigfigs>
    <significand>5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-1</exponent>
    <number>1.002e-01</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.002</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.354e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.354</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>3.682e-01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>3.682</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>1.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>1.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>2</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>9.92e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.92</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.341e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.341</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>4.718e-01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>4.718</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>1.5e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>1.5</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>3</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>9.79e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.79</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.324e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.324</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>5.993e-01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>5.993</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.0e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>2</sigfigs>
    <significand>2.0</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data></data>
   <pntnum>4</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>9.66e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.66</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.305e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.305</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>7.552e-01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>7.552</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <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></data>
   <pntnum>5</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>9.50e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>9.50</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-4</exponent>
    <number>1.284e-04</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>4</sigfigs>
    <significand>1.284</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-1</exponent>
    <number>9.442e-01</number>
    <property>Henry's Law Solubility Coefficient</property>
    <sigfigs>4</sigfigs>
    <significand>9.442</significand>
    <unit>m&lt;sup&gt;3&lt;/sup&gt; atm mol&lt;sup&gt;-1&lt;/sup&gt;</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>The multiple equilibration technique was used to measure the Henry's law constant as described by McAuliffe [1]. A known volume of pure 1,1,1-trichloroethane in a syringe was shaken with a known volume of pure water. After equilibration, the headspace was separated and analyzed for the compound of interest. A gas chromatograph fitted with an electron capture detector was used for the analysis.</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>McAuliffe, C. D.; Chem. Techn. 1971, 1, 46.</citation>
  <pubtype>paper</pubtype>
 </reference>
 <sources>
  <citation>Hunter-Smith, R. J.; Balls, P. W.; Liss, P. S.; Tellus 35B, 170 (1983).</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1111/j.1600-0889.1983.tb00021.x</url>
 </sources>
 <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>Seawater</name>
  <sample>Atlantic ocean samples, 48&amp;deg;N to 65&amp;deg;S latitudes, in late 1981.</sample>
 </substances>
 <substances>
  <casrn>71-55-6</casrn>
  <constituent>1</constituent>
  <formula>C2H3Cl3</formula>
  <inchi>InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3</inchi>
  <inchikey>UOCLXMDMGBRAIB-UHFFFAOYSA-N</inchikey>
  <molweight>133.404</molweight>
  <name>1,1,1-Trichloroethane</name>
  <sample>Source and purity not given.</sample>
 </substances>
 <system>1,1,1-Trichloroethane with Sea water</system>
 <title>Solubility data from IUPAC SDS Volume 67 (page 537) - 1,1,1-Trichloroethane with Sea water</title>
</compilation>