2-chlorophenol
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | 2-chlorophenol | ||||||||||||||||||
other names |
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Molecular formula | C 6 H 5 ClO | ||||||||||||||||||
Brief description |
Flammable liquid with an unpleasant iodoform-like smell |
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properties | |||||||||||||||||||
Molar mass | 128.56 g mol −1 | ||||||||||||||||||
Physical state |
liquid |
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density |
1.262 g cm −3 |
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Melting point |
7 ° C |
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boiling point |
174 ° C |
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Vapor pressure |
230 Pa (20 ° C) |
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pK s value |
9.11 |
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solubility |
slightly soluble in water (28.5 g l −1 at 20 ° C) |
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Refractive index |
1.5524 (20 ° C) |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
2-chlorophenol is an unpleasant, toxic liquid that smells like iodoform and belongs to the group of substances called chlorophenols . It is used in the manufacture of medicines and dyes and as a disinfectant. The compound appears as a pollutant in the groundwater.
properties
2-chlorophenol is a colorless liquid that is often yellowish to brown in color due to impurities. The liquid is sparingly soluble in water and hardly inflammable: the ignition temperature is 550 ° C.
use
2-Chlorophenol is used as an intermediate in the production of dyes and chlorinated chlorophenols.
safety instructions
The substance decomposes at higher temperatures to form hydrogen chloride , carbon monoxide and carbon dioxide . 2-chlorophenol irritates eyes, respiratory tract and skin; a corrosive effect can occur at high concentrations. The toxicity manifests itself primarily in disorders of the central nervous system .
Web links
- The degradation of 2-chlorophenol in an upflow anaerobic sludge blanket (UASB) reactor
- Committee on the Mutagenicity of Chemicals in Food Consumer Products and the Environment: Review of Genotoxicity of Chlorophenols (PDF; 334 kB)
- Factsheet (speclab)
Individual evidence
- ↑ Entry on chlorophenols. In: Römpp Online . Georg Thieme Verlag, accessed on June 15, 2014.
- ↑ a b c d e f g h i j Entry on 2-chlorophenol in the GESTIS substance database of the IFA , accessed on January 9, 2019(JavaScript required) .
- ^ Fieser and Fieser: Organic Chemistry , 2nd Edition, Verlag Chemie, Weinheim 1982, ISBN 3-527-25075-1 .
- ↑ David R. Lide (Ed.): CRC Handbook of Chemistry and Physics . 90th edition. (Internet version: 2010), CRC Press / Taylor and Francis, Boca Raton, FL, Physical Constants of Organic Compounds, pp. 3-110.
- ↑ Entry on 2-chlorophenol in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
- ↑ Analytes - 2-chlorophenol. In: chromatography-online.org. Retrieved February 5, 2016 .