<compilation>
 <compilers>Ari L. Horvath</compilers>
 <dataset>
  <points>
   <conditions>
    <exponent>1</exponent>
    <number>2.50e+01</number>
    <property>Ambient temperature</property>
    <sigfigs>3</sigfigs>
    <significand>2.50</significand>
    <unit>&amp;deg;C</unit>
   </conditions>
   <data>
    <exponent>0</exponent>
    <number>3.11e+00</number>
    <property>Amount concentration (1)</property>
    <sigfigs>3</sigfigs>
    <significand>3.11</significand>
    <unit>mol/m3</unit>
   </data>
   <pntnum>1</pntnum>
   <supplemental>
    <exponent>-2</exponent>
    <number>8.35e-02</number>
    <property>Percent mass fraction (1)</property>
    <sigfigs>3</sigfigs>
    <significand>8.35</significand>
    <unit>1</unit>
   </supplemental>
   <supplemental>
    <exponent>-5</exponent>
    <number>5.62e-05</number>
    <property>Mole fraction - Liquid (1)</property>
    <sigfigs>3</sigfigs>
    <significand>5.62</significand>
    <unit>1</unit>
   </supplemental>
  </points>
  <series>1</series>
 </dataset>
 <keywords>Solubility, Solubility data series</keywords>
 <method>Water was mixed with diiodomethanme in a glass-stoppered Erlenmeyer flask which was then placed in a constant temperature bath and rotated for 30 hours. The organic halide content of the aqueous solution was extracted with n-hexane. The optical density of the extract was measured against a nhexane blank using a Beckman spectrophotometer [1].</method>
 <publisher>The International Union of Pure and Applied Chemistry</publisher>
 <reference>
  <citation>Andrews, L. J.; Keefer, R. M.; J. Am. Chem. Soc. 1949, 71, 3644-77.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01179a018</url>
 </reference>
 <sources>
  <citation>Andrews, L. J.; Keefer, R. M.; J. Am. Chem. Soc. 1951, 73, 5733-6.</citation>
  <pubtype>paper</pubtype>
  <url>https://doi.org/10.1021/ja01156a072</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>Water</name>
  <sample>Distilled (compiler).</sample>
 </substances>
 <substances>
  <casrn>75-11-6</casrn>
  <constituent>1</constituent>
  <formula>CH2I2</formula>
  <inchi>InChI=1S/CH2I2/c2-1-3/h1H2</inchi>
  <inchikey>NZZFYRREKKOMAT-UHFFFAOYSA-N</inchikey>
  <molweight>267.836</molweight>
  <name>Diiodomethane</name>
  <sample>Prepared from iodoform at the University of California; BP = 71.0 - 71.5&amp;deg;C at 18 mmHg.</sample>
 </substances>
 <system>Diiodomethane with Water</system>
 <title>Solubility data from IUPAC SDS Volume 60 (page ?) - Diiodomethane with Water</title>
</compilation>