Paraquat

Paraquat
Paraquat-3D-balls.png
Paraquat.png
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
CAS number 1910-42-5
SMILES
InChI
Properties
Molecular formula C12H14Cl2N2
Molar mass 257.16 g/mol
Appearance off-white powder
Density 1.25 g/cm3, solid
Melting point

175 - 180 °C [1]

Boiling point

> 300 °C [1]

Solubility in water high
Hazards
Main hazards Toxic
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox references

Paraquat is the trade name for N,N'-Dimethyl-4,4'-bipyridinium dichloride, a viologen. Paraquat is used as a quaternary ammonium herbicide. It is extremely poisonous to humans if swallowed. Other members of this class include diquat, cyperquat, diethamquat, difenzoquat, and morfamquat. All of these are easily reduced to the radical ion, which generates superoxide radical that reacts with unsaturated membrane lipids.

Contents

History

Paraquat was first produced for commercial purposes in 1961 by ICI (now Syngenta) and is today among the most commonly used herbicides.

The European Union allowed Paraquat in 2004. Sweden, supported by Denmark, Austria, and Finland, brought the European Union commission to court. On 11 July 2007 the court annulled the directive authorising Paraquat as an active plant protection substance.[2]

Herbicide use

The compound is one of the most widely used herbicides in the world. It is quick-acting, non-selective, and kills green plant tissue on contact. It is redistributed within the plant but does not harm mature bark.

Being a herbicide, Paraquat protects crops by controlling a wide range of annual and certain perennial weeds that reduce crop yield and quality by competing with the crop for water, nutrients, and light.

The key characteristics that distinguish the non-selective contact herbicide Paraquat from other active ingredients used in plant protection products are:

In the United States, Paraquat is available primarily as a liquid in various strengths. It is classified as "restricted use," which means that it can be used only by licensed applicators. As with many chemicals, caution must be exercised during use.

In the European Union, Paraquat has been forbidden since July 11th 2007.

Health risks

Pure Paraquat ingested is highly toxic to mammals and humans potentially leading to acute respiratory distress syndrome (ARDS), and there are no specific antidotes. However, fuller's earth or activated charcoal is an effective treatment, if taken in time. Death may occur up to 30 days after ingestion. Diluted Paraquat used for spraying is less so, thus the greatest risk of accidental poisoning is during mixing and loading Paraquat for use.[4]

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) for these effects.[5]

Even a single swig, immediately spat out, can cause death from fibrous tissue developing in the lungs leading to asphyxiation.[6]

According to the Center 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.[7] Accidental deaths and suicides from paraquat ingestion are relatively common. For example, there have been 18 deaths in Australia from paraquat poisoning since 2000.[8]

Paraquat-induced toxicity in rats has also been linked to Parkinson's-like pathological degenerative mechanisms.[9] A study by the Buck Institute shows a connection between exposure to paraquat and iron in infancy and mid-life Parkinson's in laboratory mice.[10]

Long term exposures to Paraquat would most likely cause lung and eye damage, but reproductive/fertility damage was not found by the EPA in their review. Some suspect a possible link to a greater incidence of Parkinson's disease.

Use as a suicide agent

A large majority (93%) of fatalities from paraquat poisoning are cases of intentional self-administration, ie, suicides. In third world countries, paraquat is a "major suicide agent" (Dinham, B. 1996: Active Ingredient fact sheet, Paraquat, in: PAN UK: Pesticide News No. 32, p. 20-1: [3], 24.06.2003).

For instance, in Samoa from 1979-2001, 70% of suicides were by Paraquat poisoning. In Southern Trinidad from 1996-1997, 76% of suicides were by Paraquat.

Reference: www.pan-germany.org/download/fact_paraquat2.pdf

The reason Paraquat is such a widely used suicide agent in third-world countries is due to its widespread availability, low toxic dose (10 mLs or 2 teaspoons is enough to kill) and relative cheapness. There are campaigns to control or even ban Paraquat outright, and there are moves to restrict its availability by requiring user education and the locking up of Paraquat stores.

The fashion icon Isabella Blow committed suicide using Paraquat in 2007.

Emergency care

Persons exposed to or contaminated by Paraquat, with any suspected ingestion or absorption, should be treated by emergency medical services immediately. Prehospital care should follow these guidelines: [11]

Paraquat pot

During the late 1970s, a controversial program sponsored by the US government sprayed Paraquat on marijuana fields in Mexico.[12] Since much of this marijuana was subsequently smoked by Americans, the US government's "Paraquat Pot" program stirred much debate. Perhaps in an attempt to deter people from using marijuana, representatives of the program warned that spraying rendered the crop unsafe to smoke.

However, independent bodies have studied Paraquat in this use. Jenny Pronczuk de Garbino, [13] stated: "no lung or other injury in marijuana users has ever been attributed to Paraquat contamination". On this topic, D.P. Morgan states in a United States Environmental Protection Agency publication that: "Smoking Paraquat-contaminated marijuana does not result in lung damage as the herbicide is pyrolyzed to dipyridyl (which does not present a toxic hazard) during smoking". [14]

The EPA's glossary of terms defines Paraquat as "A standard herbicide used to kill various types of crops, including marijuana. Causes lung damage if smoke from the crop is inhaled."[15] Since Paraquat is a popular herbicide for tobacco as well, more research is needed into its effects.

References

  1. 1.0 1.1 "Paraquat dichloride". International Programme on Chemical Safety (October 2001).
  2. COURT OF FIRST INSTANCE OF THE EUROPEAN COMMUNITIES, PRESS RELEASE No° 45/07
  3. Revkin, A. C. 1983. Paraquat: A potent weed killer is killing people. Science Digest 91(6):36-38, 42, 100-104.
  4. PAN UK, Paraquat, accessed 13 October 2006.
  5. United States Environmental Protection Agency‎, [1], accessed 16 August 2007.
  6. Buzik, Shirley C.; Schiefer, H. Bruno; Irvine, Donald G. (1997). Understanding Toxicology: Chemicals, Their Benefits and Risks. Boca Raton: CRC Press. pp. 31. ISBN 0-8493-2686-9. 
  7. Center for Disease Control, Facts about Paraquat, accessed 13 October 2006.
  8. "Poisoned Latrobe," Gary Stevens, Valley Express Feb. 8, 2008.
  9. K. Ossowska, M. S'Mialowska, K. Kuter, J. Wieron'ska, B. Zieba, J. Wardas, P. Nowak, J. Dabrowska, A. Bortel, I. Biedka, G. Schulze and H. Rommelspacher (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. 
  10. Buck Institute for Aging Research (June 2007). "Combined Exposure to Environmental Toxics Accelerates Age-related Development of Parkinson's Disease in Mice". Press release.
  11. Halpin, Ted; Eric Hallman, Ellen Abend, Tonya Van Slyke (2005). Cornell Farmedic Training Program Student Manual. Ithaca, NY: Cornell University Press. 
  12. Panic over Paraquat, Time Magazine, Monday, May 1, 1978
  13. 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.
  14. 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
  15. [2]

External links