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]
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(2) Sodium hydrogen pimelate,
C7H11NaO4; [6142-21-8]
NIST WebBook
(2) Sodium hydrogen adipate,
C6H9NaO4; [18996-34-4]
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(2) Sodium hydrogen glutarate,
C5H7NaO4; [3343-88-2]
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(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]
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Original Measurements
Smagowski, H.; Zesz. Nauk. Wydz. Mat., Fiz. Chem., Univ. Gdanski, Chem. 3, 45-53 (1974).
Variables:
Ambient temperature: 298 K
Prepared by:
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:
- Source not specified; purity not specified; dried over anhydrous K2CO3 and repeatedly distilled over P2O5.
- 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.


