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| Skatole | |
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| IUPAC name | 3-methylindole |
| Other names | 4-Methyl-2,3-benzopyrrole |
| Identifiers | |
| CAS number | 83-34-1 |
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| Properties | |
| Molecular formula | C9H9N |
| Molar mass | 131.172 g/mol |
| Appearance | white crystalline solid |
| Melting point |
93-95 °C (366-369 K) |
| Boiling point |
265 °C (583 K) |
| Solubility in water | insoluble |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
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Skatole or 3-methylindole is a mildly toxic white crystalline organic compound belonging to the indole family. It occurs naturally in feces (it is produced from tryptophan in the mammalian digestive tract), beets, and coal tar, and has a strong fecal odor. In low concentrations it has a flowery smell and is found in several flowers and essential oils, including those of orange blossoms, jasmine, and Ziziphus mauritiana. It is used as a fragrance and fixative in many perfumes and as an aroma compound. Its name is derived from the Greek root skato- meaning "dung".
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Chemical properties
Skatole can be found as a white crystalline or fine powder solid, and it browns upon aging. It is nitrogenous and one of the rings is a pyrrole. It is soluble in alcohol and benzene and it gives a violet color in potassium ferrocyanide (K4Fe(CN)6·3H2O) and sulfuric acid (H2SO4). Skatole has a double ring system which displays aromaticity. It is continuous (all atoms in the ring are sp² hybridized), planar, and follows the 4n+2 rule because it has 10 π electrons. It can be synthesized through a Fischer indole synthesis which was developed by Emil Fischer.
Insect attractant
It is one of many compounds that is attractive to males of various species of orchid bees, who apparently gather the chemical to synthesize pheromones; it is commonly used as bait to attract and collect these bees for study.1
3-Methylindole has been shown to be an attractant to gravid mosquitoes in both field and laboratory conditions. Because this compound is present in feces, it is found in combined sewage overflows (CSO) as streams and lakes containing CSO water have untreated human and industrial waste. Knowledge of this attractant makes CSO sites of particular interest when studying mosquito-borne diseases such as West Nile Virus.2
Safety
Skatole has been shown to cause pulmonary edema in goats, sheep, rats, and some strains of mice. It appears to selectively target Clara cells, which are the major site of cytochrome P450 enzymes in the lungs. These enzymes convert skatole to a reactive intermediate, 3-methyleneindolenine, which damages cells by forming protein adducts.3
In a 1994 report released by five top cigarette companies, skatole was listed as one of the 599 additives to cigarettes. 4 It is added as a flavoring ingredient.
See also
- Indole
- 1-Methylindole
- 2-Methylindole (methylketol)
- 5-Methylindole
- 7-Methylindole
References
- ^ Schiestl, F.P. & Roubik, D.W. (2004). "Odor Compound Detection in Male Euglossine Bees". Journal of Chemical Ecology 29: 253–257, http://www.springerlink.com/content/kv52574k74438848/.
- ^ Beechler, J W., J G Miller, and M S Mulla (1994). "Field evaluation of synthetic compounds mediating oviposition in Culex mosquitoes (Diptera: Culicidae)". J Chem Ecol.
- ^ Miller, M; Kottler S, Ramos-Vara J, Johnson P, Ganjam V and Evans T (2003). "3-Methylindole Induces Transient Olfactory Mucosal Injury in Ponies". Veterinary Pathology 40: 363–70. doi:. PMID 12824507.
- ^ "What's in a cigarette?". Retrieved on 2006-05-31.
External links
