SDS Volume (4392)

Volume 71. Nitromethane with Water or Organic Solvents, p 1220

Original Measurements

Kimura, C.; Kashiwaya, K.; Asahara, T.; Kogyo Kagaku Zasshi 59, 1126 (1956).

Variables:

Temperature: 303 K

Prepared by:

V.P. Sazonov

Method/Apparatus/Procedure:

The titration method was used. No further experimental details were given.

Source and Purity of Materials:
  1. Synthesized in the laboratory; purity not specified; b. p. = 101°C, n(20°C, D) = 1.3817, d(20°C) = 1137.2 g L-1.
  2. Source not specified; commercial material; purity not specified; b. p. = 98°C, n(20°C, D) = 1.3878, d(20°C)
    d(20°C) = 683.2 g L-1.

Nitromethane with Heptane

Components:

(1) Nitromethane, $\ce{ CH3NO2 }$; [75-52-5] NIST WebBook
(2) Heptane, $\ce{ C7H16 }$; [142-82-5] NIST WebBook

Experimental Values:

The solubility of nitromethane in the (2)-rich phase at equilibrium at 30°C (303 K, compiler) was reported to be 100 w1 = 3.5. The corresponding mole fraction, x1, calculated by the compiler is 0.056.
The solubility of nitromethane in the (1)-rich phase at equilibrium at 30°C (303 K, compiler) was reported to be 100 w1 = 97.3. The corresponding mole fraction solubility, x1, calculated by the compiler is 0.983.

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