IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Acetonitrile with Hexane

Components:
   (1) Hexane; C6H14; [110-54-3]  NIST Chemistry WebBook for detail
   (2) Acetonitrile; C2H3N; [75-05-8]  NIST Chemistry WebBook for detail

Original Measurements:
   Sinegubova, S.I., Dissertation, Saratov University 1978.

Variables:
   Temperature = 279 K to 350 K

Prepared By:
   Valerii P. Sazonov and Nikolai V. Sazonov

Experimental Data:   (Notes on the Nomenclature)
  
Mutual solubility of acetonitrile (1) and hexane (2)
t/°CT/K102 * Mass Fraction w1Mole Fraction x1 (compiler)Comment(s)
6.0279.2--Hydrocarbon-rich phase
11.5284.72.00.041Hydrocarbon-rich phase
16.1289.3--Hydrocarbon-rich phase
19.9293.1--Hydrocarbon-rich phase
23.9297.13.00.061Hydrocarbon-rich phase
25.0298.23.70.075Hydrocarbon-rich phase
45.8319.06.00.118Hydrocarbon-rich phase
50.7323.9--Hydrocarbon-rich phase
61.1334.310.00.189Hydrocarbon-rich phase
66.7339.9--Hydrocarbon-rich phase
72.0345.2--Hydrocarbon-rich phase
73.0346.220.00.344Hydrocarbon-rich phase
75.3348.5--Hydrocarbon-rich phase
76.1349.3--Hydrocarbon-rich phase
76.3349.530.00.474Hydrocarbon-rich phase
76.9350.136.90.551Hydrocarbon-rich phase
77.0350.240.00.583Hydrocarbon-rich phase
6.0279.292.50.963Acetonitrile-rich phase
11.5284.7--Acetonitrile-rich phase
16.1289.391.10.956Acetonitrile-rich phase
19.9293.190.0*0.950Acetonitrile-rich phase
23.9297.1--Acetonitrile-rich phase
25.0298.288.30.941Acetonitrile-rich phase
45.8319.0--Acetonitrile-rich phase
50.7323.980.20.895Acetonitrile-rich phase
61.1334.3--Acetonitrile-rich phase
66.7339.970.00.831Acetonitrile-rich phase
72.0345.263.00.781Acetonitrile-rich phase
73.0346.2--Acetonitrile-rich phase
75.3348.555.10.720Acetonitrile-rich phase
76.1349.350.10.678Acetonitrile-rich phase
76.3349.5--Acetonitrile-rich phase
76.9350.145.00.632Acetonitrile-rich phase
77.0350.240.00.583 (UCST)Acetonitrile-rich phase
Notes:
   *  Value corrected by compiler from the published graphs; reported in original as 80.0.

Method/Apparatus/Procedure:
   The synthetic method was used. Sealed ampoules were placed in a glass-walled thermostat. The temperature of the thermostat was increased gradually with periodic stirring and a preliminary determination of the clear-point temperature in every ampoule was made. A more precise value of the cloud-point temperature was determined by allowing the thermostat to cool. The determination was repeated several times.

Source and Purity of Materials:
   (1) Source not specified; pure grade product; distilled over anhydrous soda, boiling point = 81.6 °C, n(20 °C, D) = 1.3441, p(25 °C) = 777 g·L–1.
   (2) Source not specified; for chromatography; not purified; boiling point = 68.8 °C, n(20 °C, D) = 1.3752, p(20 °C) = 660 g·L–1.

Estimated Errors:

   Temperature: ± 0.2 K.