Hexachlorocyclohexa-2,5-dien-1-one
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| Names | |||
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| Preferred IUPAC name
2,3,4,4,5,6-Hexachlorocyclohexa-2,5-dien-1-one | |||
| Other names
Hexachlorophenol
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| Identifiers | |||
3D model (JSmol)
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| Abbreviations | HCP | ||
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PubChem CID
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| RTECS number |
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CompTox Dashboard (EPA)
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| Properties | |||
| C6Cl6O | |||
| Molar mass | 300.77 g·mol−1 | ||
| Melting point | 113 °C (235 °F; 386 K) | ||
| Hazards[1] | |||
| GHS labelling: | |||
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| Warning | |||
| H315, H319, H335 | |||
| P261, P280, P302+P352, P305+P351+P338 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Hexachlorocyclohexa-2,5-dien-1-one, sometimes informally called hexachlorophenol (HCP), is an organochlorine compound. It can be prepared from phenol. Despite the informal name, the compound is not a phenol but is a ketone.[2] The informal name is derived from its method of preparation which includes phenol as a reagent.
Preparation
[edit]HCP is normally produced by chlorination of phenol by chlorine in the presence of metal chloride catalyst, such as ferric chloride. It can also be produced by alkaline hydrolysis of polychlorinated benzenes at high temperature and pressure, by conversion of diazonium salts of chlorinated anilines, or by chlorination of phenolsulfonic acids and benzenesulfonic acids followed by removal of the sulfonic acid group. The hydrolysis of HCP gives chloranil.[3]
References
[edit]- ^ "SAFETY DATA SHEET". ThermoFisher Scientific. 18 December 2020.
- ^ S. Gali, C. Miravitlles and M. Font-Altaba "Hexachlorocyclohexa-2,5-dienone" Acta Crystallogr. 1975, volume B31, p. 2510-2512. doi:10.1107/S0567740875007935.
- ^ François Muller; Liliane Caillard (2011). "Chlorophenols". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a07_001.pub2. ISBN 978-3527306732.