Components:

(1) Acetonitrile, C2H3N; [75-05-8] NIST WebBook
(2) Sodium hydrogen azelate, C9H15NaO4; [17356-30-8] NIST WebBook
(2) Sodium hydrogen suberate, C8H13NaO4; [27796-70-9] NIST WebBook
(2) Sodium hydrogen pimelate, C7H11NaO4; [6142-21-8] NIST WebBook
(2) Sodium hydrogen adipate, C6H9NaO4; [18996-34-4] NIST WebBook
(2) Sodium hydrogen glutarate, C5H7NaO4; [3343-88-2] NIST WebBook
(2) Sodium hydrogen succinate, C4H5NaO4; [2922-54-5] NIST WebBook
(2) Sodium hydrogen malonate, C3H3NaO4; [2922-55-6] NIST WebBook
(2) Sodium hydrogen oxalate, C2HNaO4; [1186-49-8] NIST WebBook
(2) Sodium hydrogen sebacate, C10H17NaO4; [19455-73-3] NIST WebBook

Original Measurements

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

Variables:

Ambient temperature: 298 K

Prepared by:

V.P. Sazonov

Method/Apparatus/Procedure:

The titration method was used: 25 mL of (1) and an amount of (2) exceeding the solubility were placed in 50 mL volumetric flasks. The flasks were closed by ground glass stoppers and stored at the required temperature in a thermostat for 45 hours, with intensive stirring every several hours. After this, 2 mL samples of the saturated solution were taken by pipette, diluted to 25 mL with water-less acetic acid and titrated by 0.05 N HClO4 by using crystal violet indicator.

Source and Purity of Materials:
  1. Source not specified; purity not specified; dried over anhydrous K2CO3 and repeatedly distilled over P2O5.
  2. Obtained by mixing of methanol solutions of sodium hydroxide and the acid in stoichiometric amounts; purified by crystallization from a mixture of water and methanol; purity not less 99 mass%.
Estimated Errors:

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

References

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

Experimental Values:
Solubility of monosodium salts of dicarboxylic acids (2) in acetonitrile (1) at 25.0 oC (298.2 K compiler)
C1 (mol/L) 100w2 x2
9 x 10-3 1.3 x 10-3 5 x 10-4
8 x 10-3 1.3 x 10-3 4 x 10-4
6 x 10-3 1.0 x 10-3 3 x 10-4
1.2 x 10-2 2.3 x 10-3 6 x 10-4
7 x 10-3 1.5 x 10-3 4 x 10-4
7 x 10-3 1.6 x 10-3 4 x 10-4
6 x 10-3 1.5 x 10-3 3 x 10-4
5 x 10-3 1.3 x 10-3 3 x 10-4
4 x 10-3 1.1 x 10-3 2 x 10-4

(a) For these calculations the compiler assumed that the densities of the solutions were those of acetonitrile1 at the specified temperatures.

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