Пентахлорфенол: Свойства, применение и токсичность.

the recreational dissociative drug also known as PCP
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| ImageFile = pentachlorophenol. svg
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| PIN = Pentachlorophenol
| OtherNames = Santophen, Pentachlorol, Chlorophen, Chlon, Dowicide 7, Pentacon, Penwar, Sinituho, Penta
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| PEL = TWA 0.5 mg/m3 [skin]
| LD50 = 117 mg/kg (mouse, oral)128 mg/kg (hamster, oral)17 mg/kg (rat, oral)150 mg/kg (rat, oral)
| REL = TWA 0.5 mg/m3 [skin] It can be found as pure PCP, or as the sodium salt of PCP, the latter of which dissolves easily in water. It can be biodegraded by some bacteria, including Sphingobium chlorophenolicum.

PCP has been used as a herbicide, insecticide, fungicide, algaecide, and disinfectant and as an ingredient in antifouling paint. Its use has declined due to its high toxicity and slow biodegradation. Two general methods are used for preserving wood. The pressure process method involves placing wood in a pressure treating vessel, where it is immersed in PCP and then subjected to applied pressure. In the nonpressure process method, PCP is applied by spraying, brushing, dipping, or soaking. Pentachlorophenol esters can be used as active esters in peptide synthesis, much like more popular pentafluorophenyl esters.

People may be exposed to PCP in occupational settings through the inhalation of contaminated workplace air and dermal contact with wood products treated with PCP. Also, general population exposure may occur through contact with contaminated environment media, particularly in the vicinity of wood treatment facilities and hazardous waste sites. In addition, some other important routes of exposure seem to be the inhalation of contaminated air, ingestion of contaminated ground water used as a source of drinking water, ingestion of contaminated food, and dermal contact with soils or products treated with the chemical.

PCP is quickly absorbed through the gastrointestinal tract following ingestion. Accumulation is not common, but if it does occur, the major sites are the liver, kidneys, plasma protein, spleen, and fat. Unless kidney and liver functions are impaired, PCP is quickly eliminated from tissues and blood, and is excreted, mainly unchanged or in conjugated form, via the urine. Single doses of PCP have half lives in blood of 30 to 50 hours in humans. Biomagnification of PCP in the food chain is not thought to be significant due to the fairly rapid metabolism of the compound by exposed organisms.

PCP has been detected in surface waters and sediments, rainwater, drinking water, aquatic organisms, soil, and food, as well as in human milk, adipose tissue, and urine. As PCP is generally used for its properties as a biocidal agent, considerable concern exists about adverse ecosystem effects in areas of PCP contamination. Releases to the environment are decreasing as a result of declining consumption and changing use methods. However, PCP is still released to surface waters from the atmosphere by wet deposition, from soil by run off and leaching, and from manufacturing and processing facilities. PCP is released directly into the atmosphere via volatilization from treated wood products and during production. Finally, releases to the soil can be by leaching from treated wood products, atmospheric deposition in precipitation (such as rain and snow), spills at industrial facilities, and at hazardous waste sites. After PCP is released into the atmosphere, it decomposes through photolysis. The main biodegradative pathway for PCP is reductive dehalogenation. In this process, the compound PCP is broken down to tetrachlorophenols, trichlorophenols, and dichlorophenols. Another pathway is methylation to pentachloroanisole (a more lipid soluble compound). These two methods eventually lead to ring cleavage and complete degradation. In shallow waters, PCP is also quickly removed by photolysis. In deep or turbid water processes, sorption and biodegradation take place. In reductive soil and sediments, PCP can be degraded within 14 days to 5 years, depending on the anaerobic soil bacteria that are present. However, adsorption of PCP in soils is pH dependent because it increases under acidic conditions and decreases in neutral and basic conditions.

PCP can be produced by the chlorination of phenol in the presence of catalyst (anhydrous aluminium or ferric chloride) and a temperature up to about 191 °C. This process does not result in complete chlorination and commercial PCP is only 84–90% pure. The main contaminants include other polychlorinated phenols, polychlorinated dibenzo p dioxins, and polychlorinated dibenzofurans. Some of these species are even more toxic than the PCP itself.

Pentachlorophenol is classified as a persistent organic pollutant (POP). In May 2015, countries which have signed the Stockholm Convention voted 90–2 to ban pentachlorophenol use. The United States is not a signatory and has not banned the chemical.

PCP was used in New Zealand as a timber preservative and antisapstain treatment, but since 1988 is no longer used. It was also sold as a moss killer to the general public (by Shell, at least) in the form of a 115g/L aqueous solution and labelled as a poison.

Since the early 1980s, the purchase and use of PCP in the U. S. has not been available to the general public. Nowadays, most of the PCP used in the U. S. is restricted to the treatment of utility poles and railroad ties. In the United States, any drinking water supply with a PCP concentration exceeding the MCL, 1 ppb, must be notified by the water supplier to the public. Disposal of PCP and PCP contaminated substances are regulated under RCRA as F listed (F021) or D listed (D037) hazardous wastes. Bridges and similar structures such as piers can still be treated with pentachlorophenol.

PCP was widely used in Chile until the early 1990s as a fungicide to combat the so called "blue stain" in pine timber under the name of Basilit.