Chemistry:Wurster's blue
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| Preferred IUPAC name
N1,N1,N4,N4-Tetramethylbenzene-1,4-diamine | |
Other names
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| Properties | |
| C10H16N2 | |
| Molar mass | 164.25 g/mol |
| Appearance | Colourless crystalline solid |
| Density | 0.992g/cm3 |
| Melting point | 51 °C (124 °F; 324 K) |
| Boiling point | 260 °C (500 °F; 533 K) |
| slightly in cold water more so in hot water | |
| Solubility | alcohol, chloroform |
| Acidity (pKa) | 6.35 |
| Hazards | |
| Flash point | 110 °C (230 °F; 383 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Wurster's blue is the trivial name given to the radical cation of the colorless chemical N,N,N′,N′-tetramethyl-p-phenylenediamine, also known as TMPD. This is an easily oxidised phenylenediamine, which loses two electrons in one-electron oxidation steps; the radical cation is a characteristic blue-violet colour, which gives the compound part of its name. The remaining part of its name comes from its discoverer, the German chemist Casimir Wurster (7 August 1854 – 29 November 1913).
The hydrochloride salt of TMPD finds use as a redox indicator in the oxidase test and is also used in electron transport chain analysis as it is capable of donating electrons to cytochrome c. The midpoint potential for titration of the first electron is given as 0.276 V vs Standard hydrogen electrode, and this transition is useful in potentiometric titrations as both a redox mediator and indicator. The two electron-oxidized colourless p-quinone-diiminium cation is unstable in aqueous solutions,[1] therefore highly oxidizing conditions should be avoided in titrations relying on TMPD, or reached only during the final stage of the titration. The second oxidation step is not well separated from the first on the redox scale, so some instability will be encountered on the oxidizing side of 0.276, and it is impossible to prepare pure aqueous solutions of Wurster's Blue due to its dismutation to the unstable di-iminium ion and TMPD.
References
- ↑ L. Michaelis; M. P. Schubert; S. Granick (1939). "The Free Radicals of the Type of Wurster's Salts". J. Am. Chem. Soc. 61 (8): 1981–1992. doi:10.1021/ja01877a013.
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