1,1,2-trichloroethane
Structural formula | ||||||||||||||||
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Wedges to clarify the geometry | ||||||||||||||||
General | ||||||||||||||||
Surname | 1,1,2-trichloroethane | |||||||||||||||
other names |
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Molecular formula | C 2 H 3 Cl 3 | |||||||||||||||
Brief description |
colorless volatile liquid with a pleasant odor |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 133.40 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
1.44 g cm −3 |
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Melting point |
−35.5 ° C |
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boiling point |
113.65 ° C |
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Vapor pressure |
25 h Pa (20 ° C) |
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solubility |
poor in water (4.5 g l −1 at 20 ° C) |
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Refractive index |
1.471 (20 ° C) |
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safety instructions | ||||||||||||||||
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MAK |
DFG / Switzerland: 10 ml m −3 or 55 mg m −3 |
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Thermodynamic properties | ||||||||||||||||
ΔH f 0 |
−190.8 kJ / mol |
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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 |
1,1,2-Trichloroethane is an organic compound from the group of organochlorine compounds and aliphatic chlorinated hydrocarbons. It is isomeric to 1,1,1-trichloroethane .
Extraction and presentation
1,1,2-trichloroethane can be produced by further chlorination of 1,2-dichloroethane .
properties
1,1,2-trichloroethane is a sweet-smelling liquid that is poorly soluble in water. Their vapors are much heavier (4.61 times as heavy) than air.
1,1,2-trichloroethane decomposes on intense heating or in bright light, producing various chlorine compounds (e.g. hydrogen chloride , phosgene ).
use
1,1,2-Trichloroethane is mainly used as an intermediate in the production of other organochlorine compounds such as vinylidene chloride (by splitting off HCl). As a solvent , it has only limited use for dissolving chlorinated rubber .
safety instructions
1,1,2-trichloroethane is very toxic to the heart, liver and kidneys. The use of 1,1,2-trichloroethane in products outside of chemical plants or in products from which a release is possible is prohibited.
See also
Individual evidence
- ↑ a b c d e f g h i j Entry on 1,1,2-trichloroethane in the GESTIS substance database of the IFA , accessed on January 8, 2018(JavaScript required) .
- ↑ Data sheet 1,1,2-trichloroethane from Sigma-Aldrich , accessed on March 5, 2011 ( PDF ).
- ↑ Entry on 1,1,2-trichloroethane in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on February 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
- ↑ Swiss Accident Insurance Fund (Suva): Limit values - current MAK and BAT values (search for 79-00-5 or 1,1,2-trichloroethane ), accessed on November 2, 2015.
- ↑ David R. Lide (Ed.): CRC Handbook of Chemistry and Physics . 90th edition. (Internet version: 2010), CRC Press / Taylor and Francis, Boca Raton, FL, Standard Thermodynamic Properties of Chemical Substances, pp. 5-22.
- ↑ Description of important alkenes and their preparation .
- ↑ record at enius .
- ↑ Information on diseases caused by halogenated hydrocarbons from the University of Rostock ( Memento from February 10, 2012 in the Internet Archive ).
- ↑ Directive 76/769 / EEC for dangerous substances ( Memento of September 29, 2007 in the Internet Archive ).