para-Dimethylaminobenzaldehyde
 | |
| Names | |
|---|---|
| IUPAC name
4-Dimethylaminobenzaldehyde | |
| Other names
p-Dimethylaminobenzaldehyde; 4-Formyl-N,N-dimethylaniline; N,N-Dimethyl-4-formylaniline | |
| Identifiers | |
100-10-7  | |
| ChemSpider | 7199 |
| |
| Jmol-3D images | Image |
| PubChem | 7479 |
| |
| Properties | |
| Molecular formula |
C9H11NO |
| Molar mass | 149.19 g·mol−1 |
| Appearance | yellow-white powder |
| Density | 1.1 g/mL |
| Melting point | 74 °C (165 °F; 347 K) |
| Boiling point | 176 to 177 °C (349 to 351 °F; 449 to 450 K) |
| 0.3 g/L | |
| Hazards | |
| MSDS | External MSDS |
| EU classification |  Xn |
| Flash point | 164 °C (327 °F; 437 K) |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
| Infobox references | |
para-Dimethylaminobenzaldehyde is an organic compound containing amine and aldehyde moieties which is used in Ehrlich's reagent and Kovac's reagent to test for indoles. The carbonyl group typically reacts with the electron rich 2-position of the indole but may also react at the C-3 or N-1 positions.[1]
It may also be used for determination of hydrazine.
Urobilinogen determination
It is used in Ehrlich's reagent, which may be used as a stain in thin layer chromatography, or as a reagent to detect urobilinogen in fresh, cool urine. If a urine sample is left to oxidize in air to form urobilin the reagent will not detect the urobilinogen. By adding few drops of reagent to 3 mL of urine in a test tube one can see a change of color, to dark pink or red. The degree of color change is proportional to the amount of urobilinogen in the urine sample.
Ehrlich's reagent is a strong electrophile which reacts with the electron-rich α-carbon (2-position) of indole rings to form a blue-colored adduct. It can be used to detect the presence of indole alkaloids. Not all indole alkaloids give a colored adduct as result of steric hindrance which does not allow the reaction to proceed.
Hydrazine determination
p-Dimethylaminobenzaldehyde reacts with hydrazine to form an azo-dye, which has a distinct yellow color. It is therefore used for spectrophotometric determination of hydrazine in aqueous solutions at 457 nm.[2]
Isaac Asimov essay
Isaac Asimov, in a 1963 humorous essay entitled "You, too, can speak Gaelic,",[3] reprinted in the anthology Adding a Dimension among others, traces the etymology of each component of the chemical name "para-di-methyl-amino-benz-alde-hyde" (e.g. the syllable "-benz-" ultimately derives from the Arabic lubān jāwī (لبان جاوي, "frankincense from Java"). Asimov points out that the name can be pronounced to the tune of the familiar jig "The Irish Washerwoman", and relates an anecdote in which a receptionist of Irish descent, hearing him singing the syllables thus, mistook them for the original Gaelic words to the jig. This essay inspired Jack Carroll's 1963 filk song "The Chemist's Drinking Song," (NESFA Hymnal Vol. 2 2nd ed. p. 65) set to the tune of that jig, which begins "Paradimethylaminobenzaldehyde, / Sodium citrate, ammonium cyanide, / ..."[4]
See also
References
- ↑ Ehmann, A. (1977). "The van URK-Salkowski reagent — a sensitive and specific chromogenic reagent for silica gel thin-layer chromatographic detection and identification of indole derivatives" (PDF). Journal of Chromatography A 132 (2): 267–201. doi:10.1016/S0021-9673(00)89300-0.
- ↑ G. W. Watt, J. D. Chrisp (1952). "A spectrophotometric method for determination of hydrazine". Anal. Chem. 24 (12): 2006–2008. doi:10.1021/ac60072a044.
- ↑ Asimov, Isaac (March 1963). "You, too, can speak Gaelic". The Magazine of Fantasy and Science Fiction 24 (3): 72–81.
- ↑ Carroll, John A. (1963). "The Chemist's Drinking Song". Dagonell's Bardic Notebook. David P. Salley. Retrieved 14 May 2013.