Chloroacetonitrile
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Chloroacetonitrile | |||||||||||||||
other names |
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Molecular formula | C 2 H 2 ClN | |||||||||||||||
Brief description |
colorless liquid with a pungent odor |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 75.50 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
1.193 g cm −3 |
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boiling point |
123-124 ° C |
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Vapor pressure |
11.5 mbar (20 ° C) |
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solubility |
soluble in water (100 g l −1 ) |
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Refractive index |
1.422 (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 |
Chloracetonitrile is a chemical compound from the group of nitriles . It is the nitrile of chloroacetic acid .
presentation
Chloracetonitrile can be obtained by reacting chloracetamide with phosphorus pentoxide .
properties
Chloracetonitrile is a colorless and volatile liquid at room temperature that has a pungent odor. This is completely soluble in water up to 100 grams per liter. The vapor from chloroacetonitrile is irritating.
use
Today chloroacetonitrile is used in a mixture with triethylamine as a hydrogen chloride acceptor. In the past, chloroacetonitrile was also used as a fumigant .
safety instructions
The vapors of chloroacetonitrile can form explosive mixtures with air when heated above the flash point (54 ° C) . Chloracetonitrile is very hazardous to the aquatic environment, it has been classified as water hazard class 3.
See also
- Trichloroacetonitrile (a related halogenated nitrile).
Individual evidence
- ↑ a b c d e f g h i j k l Entry on chloroacetonitrile in the GESTIS substance database of the IFA , accessed on April 6, 2016(JavaScript required) .
- ↑ Data sheet Chloroacetonitrile, 99% from Sigma-Aldrich , accessed on November 8, 2014 ( PDF ).
- ↑ Entry on chloroacetonitrile 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 .
- ↑ Ahluwalia, VK Ahluwalia, Pooja Bhagat, Renu Aggarwal, Ramesh Chandra: Intermediates for Organic Synthesis . IK International Publishing House Pvt. Ltd., 2005, p. 300 ( limited preview in Google Book Search).
- ↑ S. Gangolli, Royal Society of Chemistry (Great Britain): The Dictionary of Substances and Their Effects: C . Royal Society of Chemistry, 1999, pp. 265 ( limited preview in Google Book search).