Organochloride
Encyclopedia : O : OR : ORG : Organochloride
An organochloride is an organic compound containing at least one covalently bonded chlorine atom. Their wide structural variety and divergent chemical properties lead to a broad range of uses.
The simplest form of organochlorides are chlorinated hydrocarbons. These consist of simple hydrocarbons in which one or more hydrogen atoms have been replaced with chlorine. Most low molecular weight chlorinated hydrocarbons such as chloroform, dichloromethane, dichloroethene and trichloroethane are useful as solvents.
Many organochlorides have significant biological activities. For example, many powerful and effective insecticides are organochlorides. Common examples include dioxin, DDT, dicofol, heptachlor, endosulfan, chlordane, mirex and pentachlorophenol.
Polychlorinated biphenyls were once commonly used electrical insulators and heat transfer agents. Their use has generally been phased out due to health concerns.
Chlorinated alkenes are useful monomers used in the preparation of a variety of materials. For example, vinyl chloride is polymerized to form the plastic polyvinyl chloride (PVC).
Many organochlorides have significant toxicity. Insecticides such as dioxin and DDT are persistent organic pollutants which pose dangers to the environment. Chlorinated solvents, when not handled and disposed of properly, present problems with groundwater pollution. Some organochlorides such as phosgene have even been used as chemical warfare agents. However, the presence of chlorine in an organic compound does not ensure toxicity. Some organochlorides are safe enough for consumption in foods, such as the sweetener sucralose (Splenda).
See also
External links
- ["Formation of Chlorinated Hydrocarbons in Weathering Plant Material" article at SLAC website]
- ["The oxidation of chlorinated hydrocarbons" article from The Institute for Green Oxidation Chemistry at the Carnegie Mellon University website]
From Wikipedia, the Free Encyclopedia. Original article here. Support Wikipedia by contributing or donating.
All text is available under the terms of the GNU Free Documentation License See Wikipedia Copyrights for details.
