Paraquat

This article is about the herbicide. For the British military operation to recapture South Georgia, see Operation Paraquet.
Paraquat
Names
IUPAC name
1,1'-Dimethyl-4,4'-bipyridinium dichloride
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.
Identifiers
1910-42-5 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:34905 N
ChEMBL ChEMBL458019 YesY
ChemSpider 15146 YesY
ECHA InfoCard 100.016.015
4552
PubChem 15938
UNII 2KZ83GSS73 YesY
Properties
C12H14Cl2N2
Molar mass 257.16 g·mol−1
Appearance Yellow solid[1]
Odor faint, ammonia-like[1]
Density 1.25 g/cm3
Melting point 175 to 180 °C (347 to 356 °F; 448 to 453 K)[2]
Boiling point > 300 °C (572 °F; 573 K)[2]
High
Vapor pressure <0.0000001 mmHg (20°C)[1]
Hazards
Main hazards Toxic, environmental hazard
Safety data sheet Aldrich MSDS
GHS pictograms
H301, H311, H315, H319, H330, H335, H372, H410[3]
P260, P273, P280, P284, P301+310, P305+351+338
T+ N
R-phrases R24/25, R26, R36/37/38, R48/25, R50/53
S-phrases (S1/2), S22, S28, S36/37/39, S45, S60, S61
Lethal dose or concentration (LD, LC):
57 mg/kg (rat, oral)
120 mg/kg (mouse, oral)
25 mg/kg (dog, oral)
22 mg/kg (guinea pig, oral)[4]
3 mg/m3 (mouse, 30 min respirable dust)
3 mg/m3 (guinea pig, 30 min respirable dust)[4]
1 mg/m3 (rat, respirable dust, 6 hr)
6400 mg/m3 (rat, nonrespirable dust, 4 hr)[4]
US health exposure limits (NIOSH):
PEL (Permissible)
 TWA 0.5 mg/m3 (resp) [skin][1]
REL (Recommended)
 TWA 0.1 mg/m3 (resp) [skin][1]
IDLH (Immediate danger)
 1 mg/m3[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Paraquat (trivial name; /ˈpærəkwɑːt/) or N,N′-dimethyl-4,4′-bipyridinium dichloride (systematic name) is the organic compound with the chemical formula [(C6H7N)2]Cl2. It is classified as a viologen, a family of redox-active heterocycles of 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.[5][6] The name is derived from the para positions of the quaternary nitrogens. Quantities are sometimes expressed by cation mass alone (paraquat cation, paraquat ion); other salts (with other anions besides chloride) exist. In fact, its redox activity, which produces superoxide anions, is why it is toxic.

Production

Pyridine is coupled by treatment with sodium in ammonia followed by oxidation. The resulting 4,4'-bipyridine is then methylated with chloromethane to give the title compound:[7]

Herbicide use

Although first synthesized in 1882, paraquat's herbicidal properties were not recognized until 1955.[8] 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.[9]

Paraquat is classified as non-selective contact herbicide. The key characteristics that distinguish it from other agents used in plant protection products are:

These properties led to paraquat being used in the development of no-till farming.[12][13][14] Current research into no-till farming using mulching techniques as a substitute for herbicide application are producing good results[15]

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.[9]

Reactivity and mode of action

Paraquat is an oxidant that interferes with electron transfer, a process that is common to all life. Addition of one electron gives the radical cation:

[MV]2+ + e− [MV]+

The radical cation is also susceptible to further reduction to the neutral [MV]0:[16]

[MV]+ + e− [MV]0

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 restart the cycle.[17]

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.[18]

Weed resistance management

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.[19][20]

One example is the "Double Knock" system used in Australia.[21] 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.[22] Nevertheless, herbicide resistance has been seen for both herbicides in Western Australia.[23]

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.[24] 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.

Toxicity

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 have been some successful cases of using cyclophosphamide (Endoxan) to treat paraquat poisoning.[25] 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.[8]

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.[26]

The alveolar epithelial cells of the lung selectively concentrates paraquat.[27] Even a single swig, immediately spat out, can cause death from fibrous tissue developing in the lungs, leading to asphyxiation.[28]

One of the characters in the infamous British public information film Apaches (1977) dies hours after accidentally swallowing a small amount; the paraquat in the film is contained in a receptacle similar to a whisky bottle.

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.[29] Accidental deaths and suicides from paraquat ingestion are relatively common. For example, there have been 18 deaths in Australia from paraquat poisoning since 2000.[30] 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.

"Paraquat pot"

During the late 1970s, a controversial program sponsored by the US government sprayed paraquat on cannabis fields in Mexico.[31] Mexico began efforts to eradicate marijuana and poppy fields in 1975. US gov helped by sending helicopters and tech assistance. Helicopters were used to spray herbicides paraquat and 2,4-D on the fields and contaminated pot began to show up in US market.[32] 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".[33] 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."[34]

Use in suicide and murder

A large majority (93 percent) of fatalities from paraquat poisoning are suicides, which occur mostly in developing countries.[35] For instance, in Samoa from 1979–2001, 70 percent of suicides were by paraquat poisoning. Trinidad and Tobago is particularly well known for its incidence of suicides involving the use of Gramoxone (commercial name of paraquat). In southern Trinidad, particularly in Penal, Debe from 1996–1997, 76 percent of suicides were by paraquat, 96 percent of which involved the over-consumption of alcohol such as rum.[36] Fashion celebrity Isabella Blow committed suicide using paraquat in 2007. Paraquat is widely used as a suicide agent in third-world countries because it is widely available at low cost. Further, 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.[37]

Parkinson's disease

In 2011, a US National Institutes of Health study showed a link between paraquat use and Parkinson's disease in farm workers.[38] 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.[5] Paraquat-induced toxicity in rats has also been linked to Parkinson's-like neurological degenerative mechanisms.[39] 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.[40]

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.[41]

References

  1. 1 2 3 4 5 6 "NIOSH Pocket Guide to Chemical Hazards #0478". National Institute for Occupational Safety and Health (NIOSH).
  2. 1 2 "Paraquat dichloride". International Programme on Chemical Safety. October 2001.
  3. ↑ Sigma-Aldrich Co., 1,1′-Dimethyl-4,4′-bipyridinium dichloride hydrate. Retrieved on 2015-03-29.
  4. 1 2 3 "Paraquat". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
  5. 1 2 "Two pesticides -- rotenone and paraquat -- linked to Parkinson's disease, study suggests". sciencedaily.com. 2011. Retrieved October 25, 2011.
  6. ↑ Kamel, F. (2013). "Paths from Pesticides to Parkinson's". Science. 341 (6147): 722–723. doi:10.1126/science.1243619. PMID 23950519.
  7. ↑ "Paraquat and Diquat". IPCS INCHEM.
  8. 1 2 "Paraquat". Pesticides News. 32: 20–21. 1996.
  9. 1 2 COURT OF FIRST INSTANCE OF THE EUROPEAN COMMUNITIES, PRESS RELEASE No° 45/07
  10. ↑ Coats, G. E.; Funderburk, Jr., H. H.; Lawrence, J. M.; Davis, D. E. (28 July 2006). "Factors Affecting Persistence and Inactivation of Diquat and Paraquat". Weed Research. 6 (1): 58–66. doi:10.1111/j.1365-3180.1966.tb00867.x. Retrieved 3 April 2014.
  11. ↑ Revkin, A. C. (1983). "Paraquat: A potent weed killer is killing people". Science Digest. 91 (6): 36–38.
  12. ↑ Hood A. E. M.; Jameson H. R.; Cotterell R. (1963). "This technique involved destruction of pastures by herbicides such as paraquat as a substitute for ploughing". Nature. 197 (4869): 381.
  13. ↑ Hood A. E. M. (1965). Ploughless farming using "Gramoxone". Outlook on Agriculture IV, 6, 286–294
  14. ↑ Huggins D R & Reganold J. P. (2008). No-Till: the Quiet Revolution. Scientific American, July 2008, pp 70–77
  15. ↑ Halde, Caroline. "How to make organic no-till work for field crops in Southern Manitoba". natural systems agriculture. University of Manitoba. Retrieved 3 April 2014.
  16. ↑ Bockman T. M.; Kochi J. K. (1990). "Isolation and oxidation-reduction of methylviologen cation radicals. Novel disproportionation in charge-transfer salts by X-ray crystallography". J. Org. Chem. 55: 4127–4135. doi:10.1021/jo00300a033.
  17. ↑ Summers L.A. (1980) The Bipyridinium Herbicides. Academic Press, New York, NY.
  18. ↑ Bus; Gibson, JE; et al. (1984). "Paraquat: model for oxidant-initiated toxicity". Environmental Health Perspectives. 55: 37–46. doi:10.1289/ehp.845537. PMC 1568364Freely accessible. PMID 6329674.
  19. ↑ Beckie, H. J. (2011). "Herbicide-resistant weed management: Focus on glyphosate". Pest Management Science: n/a. doi:10.1002/ps.2195.
  20. ↑ Eubank, T. W.; Poston, D. H.; Nandula, V. K.; Koger, C. H.; Shaw, D. R.; Reynolds, D. B. (2008). "Glyphosate-resistant Horseweed (Conyza canadensis) Control Using Glyphosate-, Paraquat-, and Glufosinate-Based Herbicide Programs". Weed Technology. 22: 16–21. doi:10.1614/WT-07-038.1.
  21. ↑ Borger C.P.; Hashem A. (2007). "Evaluating the double knockdown technique: sequence, application interval, and annual ryegrass growth stage". Australian Journal of Agricultural Research. 58: 265–271. doi:10.1071/ar05373.
  22. ↑ Walsh, M. J.; Powles, S. B. (2007). "Management Strategies for Herbicide-resistant Weed Populations in Australian Dryland Crop Production Systems". Weed Technology. 21 (2): 332–338. doi:10.1614/WT-06-086.1.
  23. ↑ in ryegrass
  24. ↑ Neve, P.; Diggle, A. J.; Smith, F. P.; Powles, S. B. (2003). "Simulating evolution of glyphosate resistance in Lolium rigidum II: Past, present and future glyphosate use in Australian cropping". Weed Research. 43 (6): 418–427. doi:10.1046/j.0043-1737.2003.00356.x.
  25. ↑ Newstead CG (1996). "Cyclophosphamide treatment of paraquat poisoning". Thorax. 51: 659–60. doi:10.1136/thx.51.7.659. PMC 472483Freely accessible. PMID 8882068.
  26. ↑ Paraquat Dichloride, United States Environmental Protection Agency, accessed 16 August 2007.
  27. ↑ Kliegman. Nelson's Textbook of Pediatrics (19 ed.). Elsevier. ISBN 978-1-4377-0755-7.
  28. ↑ Buzik, Shirley C.; Schiefer, H. Bruno; Irvine, Donald G. (1997). Understanding Toxicology: Chemicals, Their Benefits and Risks. Boca Raton: CRC Press. p. 31. ISBN 0-8493-2686-9.
  29. ↑ Centers for Disease Control, Facts about Paraquat, accessed 13 October 2006.
  30. ↑ "Poisoned Latrobe," Gary Stevens, Valley Express Feb. 8, 2008.
  31. ↑ Panic over Paraquat, Time Magazine, May 1, 1978
  32. ↑ "Drug Survival News". 6 (5). March 1978.
  33. ↑ Pronczuk de Garbino J, Epidemiology of paraquat poisoning, in: Bismuth C, and Hall AH (eds), Paraquat Poisoning: Mechanisms, Prevention, Treatment, pp. 37-51, New York: Marcel Dekker, 1995.
  34. ↑ Reigart, J. Routt and Roberts, James R. Recognition and Management of Pesticide Poisonings, 5th edition. Washington, DC: United States Environmental Protection Agency, 1999. Book available online
  35. ↑ Dinham, B. (1996). "Active Ingredient fact sheet, Paraquat". Pesticide News. 32: 20–21.
  36. ↑ Paraquat and Suicide, Pestizid Aktions-Netzwerk e.V. (PAN Germany).
  37. ↑ Emsley, John. Molecules of Murder: Criminal Molecules and Classic Cases. Royal Society of Chemistry Publishing, 2008, p.195
  38. ↑ Tanner, C. M.; Kamel, F.; et al. (2011). "Rotenone, Paraquat, and Parkinson's Disease". Environmental Health Perspectives. 119 (6): 866–872. doi:10.1289/ehp.1002839. PMC 3114824Freely accessible. PMID 21269927.
  39. ↑ Ossowska, K.; Smiałowska, M.; et al. (2006). "Degeneration of dopaminergic mesocortical neurons and activation of compensatory processes induced by a long-term paraquat administration in rats: Implications for Parkinson's disease". Neuroscience. 141 (4): 2155–2165. doi:10.1016/j.neuroscience.2006.05.039. PMID 16797138.
  40. ↑ "Combined Exposure to Environmental Toxics Accelerates Age-related Development of Parkinson's Disease in Mice" (Press release). Buck Institute for Aging Research. June 2007.
  41. ↑ T.Z. Rzezniczak; L.A. Douglas; J.H. Watterson; T.J.S. Merritt (2011). "Paraquat administration in Drosophila for use in metabolic studies of oxidative stress". Analytical Biochemistry (journal). 419 (2): 345–347. doi:10.1016/j.ab.2011.08.023. PMID 21910964.

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External links

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