出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/10/17 14:10:34」(JST)
| Paraquat | |
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IUPAC name
1,1'-Dimethyl-4,4'-bipyridinium dichloride |
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Other names
Paraquat dichloride; Methyl viologen dichloride; Crisquat; Dexuron; Esgram; Gramuron; Ortho Paraquat CL; Para-col; Pillarxone; Tota-col; Toxer Total; PP148; Cyclone; Gramixel; Gramoxone; Pathclear; AH 501. |
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| Identifiers | |
| CAS number | 1910-42-5 Y |
| PubChem | 15938 |
| ChemSpider | 15146 Y |
| UNII | 2KZ83GSS73 Y |
| ChEBI | CHEBI:34905 N |
| ChEMBL | CHEMBL458019 Y |
| Jmol-3D images | Image 1 |
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SMILES
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InChI
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| Properties | |
| Molecular formula | C12H14Cl2N2 |
| Molar mass | 257.16 g mol−1 |
| Appearance | White powder |
| Density | 1.25 g/cm3 |
| Melting point | 175-180 °C[1] |
| Boiling point | >300 °C[1] |
| Solubility in water | High |
| Hazards | |
| MSDS | Oxford MSDS |
| Main hazards | Toxic |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| N (verify) (what is: Y/N?) | |
| Infobox references | |
Paraquat is the trade name for N,N′-dimethyl-4,4′-bipyridinium dichloride, is the organic compound with the formula [(C5H4N)2]Cl2. It is classified as a viologen, a family of redox-active heterocycles or similar structure. This salt is one of the most widely used herbicides. It is quick-acting and non-selective, killing green plant tissue on contact. It is also toxic to human beings and animals. It is linked to development of Parkinson's disease.[2][3] The name is derived from the para positions of the quaternary nitrogens. A variety of related compounds are used in textiles.
Pyridine is coupled by treatment with sodium amide followed by oxidation. The resulting 4,4'-bipyridine, which is then methylated with chloromethane to give the desired compound:[4]
Although first synthesized in 1882, paraquat's herbicidal properties were not recognized until 1955.[5] Paraquat was first manufactured and sold by ICI in early 1962, and is today among the most commonly used herbicides.
The European Union approved the use of paraquat in 2004 but Sweden, supported by Denmark, Austria, and Finland, appealed this decision. In 2007, the court annulled the directive authorizing paraquat as an active plant protection substance stating that the 2004 decision was wrong in finding that there were no indications of neurotoxicity associated with paraquat and that the studies about the link between paraquat and Parkinson's disease should have been considered.[6]
The key characteristics that distinguish the non-selective contact herbicide paraquat from other active ingredients used in plant protection products are:
These properties led to paraquat being used in the development of no-till farming.[9][10][11] Current research into no-till farming using mulching techniques as a substitute for herbicide application are producing good results[12]
In the United States, paraquat is available primarily as a solution in various strengths. It is classified as "restricted use," which means that it can be used by licensed applicators only. In the European Union, paraquat has been forbidden since 2007.[6]
Paraquat interferes with electron transfer, a process that is common to all life. It is an electron acceptor in redox and radical reactions.
As an herbicide, paraquat acts by inhibiting photosynthesis. In light-exposed plants, it accepts electrons from photosystem I (more specifically Fd, which is presented with electrons from PS I) and transfers them to molecular oxygen. In this manner, destructive reactive oxygen species are produced. In forming these reactive oxygen species, the oxidized form of paraquat is regenerated, and is again available to shunt electrons from photosystem I to start the cycle again.[13]
Paraquat is often used in science to catalyze the formation of reactive oxygen species (ROS), more specifically, the superoxide free radical. Paraquat will undergo redox cycling in vivo, being reduced by an electron donor such as NADPH, before being oxidized by an electron receptor such as dioxygen to produce superoxide, a major ROS.[14]
Problems with herbicide resistant weeds may be addressed by applying herbicides with different modes of action, along with cultural methods such as crop rotation, in integrated weed management (IWM) systems. Paraquat, with its distinctive mode of action, is one of few chemical options that can be used to prevent and mitigate problems with weeds that have become resistant to the very widely used non-selective herbicide glyphosate.[15][16]
One example is the "Double Knock" system used in Australia.[17] Before planting a crop, weeds are sprayed with glyphosate first, then followed seven to ten days later by a paraquat herbicide. Although twice as expensive as using a single glyphosate spray, the "Double Knock" system is an important resistance management strategy widely relied upon by farmers.[18] Although herbicide resistance has been seen for both herbicides in Western Australia in ryegrass
A computer simulation showed that with alternating annual use between glyphosate and paraquat, only one field in five would be expected to have glyphosate-resistant annual ryegrass (Lolium rigidum) after 30 years, compared to nearly 90% of fields sprayed only with glyphosate.[19] A "Double Knock" regime with paraquat cleaning-up after glyphosate was predicted to keep all fields free of glyphosate resistant ryegrass for at least 30 years.
During the late 1970s, a controversial program sponsored by the US government sprayed paraquat on cannabis fields in Mexico.[20] Since much of this cannabis was subsequently smoked by Americans, the US government's "Paraquat Pot" program stirred much debate. Perhaps in an attempt to deter people from using cannabis, representatives of the program warned that spraying rendered the crop unsafe to smoke. However, a 1995 study found that "no lung or other injury in cannabis users has ever been attributed to paraquat contamination".[21] Also a United States Environmental Protection Agency manual states: "... toxic effects caused by this mechanism have been either very rare or nonexistent. Most paraquat that contaminates cannabis is pyrolyzed during smoking to dipyridyl, which is a product of combustion of the leaf material itself (including cannabis) and presents little toxic hazard."[22]
Pure paraquat, when ingested, is highly toxic to mammals, including humans; potentially leading to acute respiratory distress syndrome (ARDS). Although there are no specific antidotes, fuller's earth or activated charcoal is an effective treatment if taken in time. There were also some successful cases of using cyclophosphamide (Endoxan) to treat Paraquat poisoning.[23] Death may occur up to 30 days after ingestion. Diluted paraquat used for spraying is less toxic; thus, the greatest risk of accidental poisoning is during mixing and loading paraquat for use.[5]
In acute toxicity studies using laboratory animals, paraquat has been shown to be highly toxic by the inhalation route and has been placed in Toxicity Category I (the highest of four levels) for acute inhalation effects. However, the EPA has determined that particles used in agricultural practices (400 to 800 μm) are well beyond the respirable range and therefore inhalation toxicity is not a toxicological endpoint of concern. Paraquat is toxic (Category II) by the oral route and moderately toxic (Category III) by the dermal route. Paraquat will cause moderate to severe eye irritation and minimal dermal irritation, and has been placed in Toxicity Categories II and IV (slightly toxic) respectively for these effects.[24]
Even a single swig, immediately spat out, can cause death from fibrous tissue developing in the lungs, leading to asphyxiation.[25]
According to the Centers for Disease Control, ingesting paraquat causes symptoms such as liver, lung, heart, and kidney failure within several days to several weeks that can lead to death up to 30 days after ingestion. Those who suffer large exposures are unlikely to survive. Chronic exposure can lead to lung damage, kidney failure, heart failure, and oesophageal strictures.[26] Accidental deaths and suicides from paraquat ingestion are relatively common. For example, there have been 18 deaths in Australia from paraquat poisoning since 2000.[27] Long term exposures to paraquat would most likely cause lung and eye damage, but reproductive/fertility damage was not found by the United States Environmental Protection Agency (EPA) in their review.
A large majority (93%) of fatalities from paraquat poisoning are suicides, which occur mostly in developing countries.[28] For instance, in Samoa from 1979–2001, 70% of suicides were by paraquat poisoning. Trinidad and Tobago is particularly well known for its incidence of suicides involving the use of gramoxone. In southern Trinidad, particularly in Penal, Debe from 1996–1997, 76% of suicides were by paraquat, 96% of which involve the over-consumption of alcohol such as rum.[29] Fashion celebrity Isabella Blow committed suicide using paraquat in 2007. Paraquat is widely used suicide agent in third-world countries because it is widely available at low cost. Furthermore the toxic dose is low (10 mL or 2 teaspoons is enough to kill). Campaigns exist to control or even ban paraquat, and there are moves to restrict its availability by requiring user education and the locking up of paraquat stores.
The indiscriminate paraquat murders, which occurred in Japan in 1985, were carried out using paraquat as a poison.
Paraquat, as the weedkiller Gramoxone, was used in the UK in 1981 by Susan Barber to poison the gravy of her husband Michael's pie. She was convicted of murder in November 1982, maintaining throughout that she had not intended to kill him.[30]
In 2011, a US National Institutes of Health study showed a link between paraquat use and Parkinson's disease in farm workers.[31] A co-author of the paper said that paraquat increases production of certain oxygen derivatives that may harm cellular structures, and that people who used paraquat, or other pesticides with a similar mechanism of action, were more likely to develop Parkinson's.[2] Paraquat-induced toxicity in rats has also been linked to Parkinson's-like neurological degenerative mechanisms.[32] A study by the Buck Institute for Research on Aging showed a connection between exposure to paraquat and iron in infancy and mid-life Parkinson's in laboratory mice.[33]
Paraquat is structurally similar to MPP+, a known fast-acting inducer of Parkinson's disease in primate brains. The chloride of MPP+ was sold under the trade name Cyperquat.
Paraquat also induces oxidative stress in invertebrates such as Drosophila melanogaster. Paraquat-fed flies suffer early-onset mortality, and significant increases in superoxide dismutase activity.[34]
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