SDS Volume

Volume 71. Nitromethane with Water or Organic Solvents, p None

Source Publication

Smagowski, H.; Zesz. Nauk. Wydz. Mat., Fiz. Chem., Univ. Gdanski, Chem. 3, 45-53 (1974).

Conditions:

Room Temp: 273 - 308 $\pu{K}$

Compiler:

V.P. Sazonov

Methodology:

The titration method was used: 25 mL of [1] and an amount of (2) exceeding the solubility were placed into 50 mL volumetric flasks. The flasks were closed by ground stoppers and were stored at the required temperature in a thermostat for 45 hours, with intensive stirring every several hours. After this, 5 mL samples of the saturated solution were taken by pipette, diluted to 25 mL with nitromethane and titrated against 0.07 N tetrabutylammonium hydroxide solution by using bromothymol blue indicator.

Sample Information:
  1. Source not specified; purity not specified; dried over $\ce{P2O5}$ and distilled at reduced pressure.
  2. Source not specified; purity not specified; purified by crystallization from water.
Measurement Errors:

Ambient temperature: Not reported.
Mass concentration (m/v) (1): Not reported.
Pressure: Not reported.

Methodology Citation

1 Timmermans, J.; Physico-Chemical Constants of Pure Organic Compounds (Elsevier, New York, 1950).

System Components:
  1. Nitromethane, $\ce{ CH3NO2 }$; [75-52-5] NIST WebBook
  2. Nonanedioic acid, $\ce{ C9H16O4 }$; [123-99-9] NIST WebBook
Experimental Data
$T$ (°C) $T$ ($\pu{K}$) $C_{1}$ (g/L) 100w2 $x_{2}$
0273.2 2 x 10-3 3 x 10-41 x 10-4
15.0288.2 3 x 10-3 5 x 10-42 x 10-4
25.0298.2 5 x 10-3 8 x 10-43 x 10-4
35.0308.2 8 x 10-3 1.4 x 10-34 x 10-4

(a) The densities of the solutions were taken to be by the compiler those of nitromethane (Timmermans1) at the specified temperatures.

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