IUPAC-NIST Solubility Database
NIST Standard Reference Database 106


Glass Ball as Bullet Solubility System: Nitromethane with Nitroethane and Heptane

Components:
   (1) Nitromethane; CH3NO2 ; [75-52-5]  NIST Chemistry WebBook for detail
   (2) Nitroethane; C2H5NO2; [79-24-3]  NIST Chemistry WebBook for detail
   (3) Heptane; C7H16; [142-82-5]  NIST Chemistry WebBook for detail

Original Measurements:
   Komarova. E. G.; and Kogan, V. B.; Zh. Prikl. Khim. (Leningrad) 37, 1776-86 (1964).

Variables:
   Temperature = 293 K to 343 K

Prepared By:
   V. P. Sazonov

Experimental Data:   (Notes on the Nomenclature)
  
Compositions of two coexisting liquid phases
t/°CT/KMass Fraction w1 (compiler) Mass Fraction w2 (compiler)Mole Fraction x1Mole Fraction x2Comment(s)
20.0293.20.88020.09170.90570.0767nitroalkane-rich phase
20.0293.20.77920.19050.81800.1626nitroalkane-rich phase
20.0293.20.67580.28550.72550.2492nitroalkane-rich phase
20.0293.20.57580.37650.63210.3360nitroalkane-rich phase
20.0293.20.47800.46420.53670.4238nitroalkane-rich phase
20.0293.20.37510.55540.43180.5198nitroalkane-rich phase
20.0293.20.30650.61410.35880.5846nitroalkane-rich phase
20.0293.20.24240.66730.28860.6459nitroalkane-rich phase
20.0293.20.16370.72970.19920.7218nitroalkane-rich phase
20.0293.20.08430.78600.10510.7965nitroalkane-rich phase
40.0313.20.86950.08820.89920.0742nitroalkane-rich phase
40.0313.20.76660.17780.81120.1530nitroalkane-rich phase
40.0313.20.66410.26560.71960.2340nitroalkane-rich phase
40.0313.20.56940.34910.63060.3144nitroalkane-rich phase
40.0313.20.45880.44680.52160.4130nitroalkane-rich phase
40.0313.20.35600.52670.41600.5005nitroalkane-rich phase
40.0313.20.29110.57670.34630.5579nitroalkane-rich phase
40.0313.20.21890.62140.26650.6151nitroalkane-rich phase
40.0313.20.14620.64910.18300.6608nitroalkane-rich phase
40.0313.20.07160.66500.09270.6998nitroalkane-rich phase
40.0313.20.04490.63690.05930.6845nitroalkane-rich phase
70.0343.20.83520.08440.87660.0720nitroalkane-rich phase
70.0343.20.72230.17900.77840.1568nitroalkane-rich phase
70.0343.20.62370.25070.68990.2255nitroalkane-rich phase
70.0343.20.50440.32100.57860.2994nitroalkane-rich phase
70.0343.20.38970.35440.46740.3456nitroalkane-rich phase
70.0343.20.28620.34800.36140.3573nitroalkane-rich phase
20.0293.20.02110.00510.03410.0067heptane-rich phase
20.0293.20.02040.01000.03300.0131heptane-rich phase
20.0293.20.01970.01660.03180.0218heptane-rich phase
20.0293.20.01880.02350.03030.0308heptane-rich phase
20.0293.20.01800.03260.02890.0425heptane-rich phase
20.0293.20.01650.04300.02640.0560heptane-rich phase
20.0293.20.01540.05120.02460.0666heptane-rich phase
20.0293.20.01380.06190.02200.0803heptane-rich phase
20.0293.20.01160.07970.01840.1029heptane-rich phase
20.0293.20.00750.10430.01180.1339heptane-rich phase
40.0313.20.03710.00820.05940.0106heptane-rich phase
40.0313.20.04000.01600.06370.0207heptane-rich phase
40.0313.20.03810.02890.06050.0373heptane-rich phase
40.0313.20.03910.04260.06170.0547heptane-rich phase
40.0313.20.03590.05990.05650.0767heptane-rich phase
40.0313.20.03810.08140.05950.0835heptane-rich phase
40.0313.20.03810.09710.05910.1226heptane-rich phase
40.0313.20.03690.11470.0500.1441heptane-rich phase
40.0313.20.03470.15570.05300.1934heptane-rich phase
40.0313.20.02720.25060.04050.3039heptane-rich phase
40.0313.20.02420.28790.03560.2562heptane-rich phase
70.0343.20.08830.01480.13660.0186heptane-rich phase
70.0343.20.09280.03450.14220.0430heptane-rich phase
70.0343.20.09930.05880.15040.0724heptane-rich phase
70.0343.20.10940.09410.16300.1140heptane-rich phase
70.0343.20.13080.15290.18920.1798heptane-rich phase
70.0343.20.17790.24150.24440.2697heptane-rich phase
Method/Apparatus/Procedure:
   The analytical method was used. Mixture of (1), (2) and (3) was placed in a thermostated cell and stirred for an hour. The composition of the phases was determined by gas chromatography.

Source and Purity of Materials:
   (1) Source not specified, pure grade reagent; distilled in 1.2 m fractionating column; b. p. = 101.2 °C; n(20 °C, D) = 1.3818,d(20 °C, 4 °C) = 1.1380.
   (2) Source not specified, pure grade reagent; distilled in 1.2 m fractionating column; b. p. = 114.0 °C; n(20 °C, D) = 1.3920, d(20 °C, 4 °C) = 1.0520.
   (3) Source not specified; pure grade reagent; distilled in 1.2 m fractionating column; b. p. = 98.4 °C; n(20 °C, D) = 1.3877, d(20 °C, 4 °C) = 0.6838.

Estimated Errors:

   Temperature: control to ± 0.1 K.