Fipronil

Fipronil
Identifiers
CAS number 120068-37-3 Y
PubChem 3352
ChemSpider 3235 Y
UNII QGH063955F Y
KEGG D01042 Y
ChEBI CHEBI:5063 Y
ChEMBL CHEMBL101326 Y
ATCvet code QP53AX15
Jmol-3D images Image 1
Properties
Molecular formula C12H4Cl2F6N4OS
Molar mass 437.15 g/mol
Density 1.477-1.626 g/cm³
Melting point

200.5 °C

 Y (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Fipronil is a broad spectrum insecticide that disrupts the insect central nervous system by blocking the passage of chloride ions through the GABA receptor and glutamate-gated chloride (GluCl) channels, components of the central nervous system. This causes hyperexcitation of contaminated insects' nerves and muscles. Specificity of fipronil on insects may come from a better efficacy on GABA receptor, but also because GluCl channels do not exist in mammals.[1]

Contents

Effects

Fipronil is a slow acting poison. When mixed with a bait, it allows the poisoned insect time to return to the colony or harborage. In cockroaches, the feces and carcass can contain sufficient residual pesticide to kill others in the same nesting site. In ants, the sharing of the bait among colony members assists in the spreading of the poison throughout the colony. With the cascading effect, the projected kill rate is about 95% in three days for ants and cockroaches.

Toxic baiting with fipronil has also been shown to be extremely effective in locally eliminating German wasps. All colonies within foraging range are completely eliminated within one week.[2]

Wildlife impacts include the following:

Fipronil is also used as the active ingredient in flea control products for pets, field pest control for corn, golf courses and commercial turf.

It acts by binding to an allosteric site of GABAA receptors and GluCl receptor (of the insect), a form of noncompetitive inhibition.

Acute oral LD50 (rat) 97 mg/kg
Acute dermal LD50 (rat) >2000 mg/kg

In animals and humans, fipronil poisoning is characterized by vomiting, agitation, and seizures, and can usually be managed through supportive care and early treatment of seizures; generally benzodiazepine use.[4][5]

In May 2003, the Direction Générale de l'Alimentation du ministère de l'Agriculture indicated a case of bee mortality observed in southern France was related to fipronil acute toxicity. Toxicity was linked to defective seed treatment, which generated dust. In February 2003, the French Ministry of Agriculture decided to temporarily suspend the sale of BASF crop protection products containing fipronil in France.[6] The seed treatment involved has since been forbidden. Fipronil was used in a broad spraying to control locusts in Madagascar in a program that began in 1997.[7]

Historical use

Fipronil was discovered and developed by Rhône-Poulenc between 1985 and 1987, and placed on the market in 1993 under the US Patent No. US 5,232,940 B2. Between 1987 and 1996, fipronil was evaluated on more than 250 insect pests on 60 crops worldwide, and crop protection accounted for about 39% of total fipronil production in 1997. Since 2003, BASF holds the patent rights for producing and selling fipronil-based products in many countries.

Fipronil, as marketed under the name Regent, is used against major lepidopteran and orthopteran pests on a wide range of field and horticultural crops and against coleopteran larvae in soils. It is also employed for cockroach and ant control under the trade names Goliath and Nexa, including in the US, where it is also used against pests of field corn, golf courses and commercial lawn (trade name Chipco Choice). It has been used under the trade name Adonis for locust control in Madagascar and in Kazakhstan.[8]

Fipronil effectively controls termite pests, and was shown to be effective in field trials in Africa and Australia, where it is marketed under the names Termidor, Ultrathor, and Taurus.

In 1999, 400,000 hectares were treated with Regent. It became the leading imported product in the area of rice insecticides, the second biggest crop protection market after cotton in China. In the UK, provisional approval for five years has been granted for fipronil use as a public hygiene insecticide.[8] Fipronil is also the main active ingredient of Frontline and PetArmour Plus, treatments used in fighting ticks and fleas infestations in dogs and cats.[9]

Ecological toxicity

Fipronil is highly toxic for crustaceans, insects and zooplankton[10], as well as bees, termites, rabbits, the fringe-toed lizard and certain groups of gallinaceous birds. It appears to reduce the longevity and fecundity of female braconid parasitoids. It is also highly toxic to many fish, though its toxicity varies with species. Conversely, the substance is relatively innocuous to passerines, wildfowl and earthworms.

Few studies of effects on wildlife have been conducted, but studies of the nontarget impact from emergency applications of fipronil as barrier sprays for locust control in Madagascar showed adverse impacts of fipronil on termites, which appear to be very severe and long-lived. There were also indications of adverse effects in the short term on several other invertebrate groups, one species of lizard (Mabuya elegans) and several species of birds (including the Madagascar bee-eater).

Nontarget effects on some insects (predatory and detritivorous beetles, some parasitic wasps and bees) were also found in field trials of fipronil for desert locust control in Mauritania, and very low doses (0.6-2.0 g a.i./ha) used against grasshoppers in Niger caused impacts on nontarget insects comparable to those found with other insecticides used in grasshopper control. The implications of this for other wildlife and ecology of the habitat remain unknown, but appear unlikely to be severe.[8]

Colony collapse disorder

Fipronil is one of the main chemical causes blamed for the spread of colony collapse disorder among bees. It has been found by the Minutes-Association for Technical Coordination Fund in France that even at very low nonlethal doses for bees, the pesticide still impairs their ability to locate their hive, resulting in large numbers of forager bees lost with every pollen-finding expedition.[11]

Toxicity

Fipronil is classed as a WHO Class II moderately hazardous pesticide, and has a rat acute oral LD50 of 97 mg/kg.

It has moderate acute toxicity by the oral and inhalation routes in rats. Dermal absorption in rats is less than 1% after 24 h and toxicity is considered to be low. It has been found to be very toxic to rabbits.

The photodegradate MB46513 appears to have a higher acute toxicity to mammals than fipronil itself by a factor of about 10.

Toxicity on humans has been tested in few studies, more commonly involving human cells which were used in carcinogenicity studies, but with no adverse effects. Yet, fipronil has been classified as a Group C (possible human) carcinogen based on an increase in thyroid follicular cell tumors in both sexes of the rat. Furthermore, fipronil is considered slightly irritating to the skin, while moderately irritating to the eyes in both humans and animals, and there is no evidence suggesting it may cause birth defects.[12]

Two Top Spot products were determined by the New York State Department of Environmental Conservation to pose no significant exposure risks to workers applying the product. However, concerns were raised about human exposure to Frontline spray treatment in 1996, leading to a denial of registration for the spray product. Commercial pet groomers and veterinarians were considered to be at risk from chronic exposure via inhalation and dermal absorption during the application of the spray, assuming they may have to treat up to 20 large dogs per day.[8] Fipronil is not volatile, so there is little likelihood of humans being exposed to this compound in the air.[12]

See also

References

  1. ^ Raymond-Delpech V, Matsuda K, Sattelle BM, Rauh JJ, Sattelle DB (2005) Ion channels: molecular targets of neuroactive insecticides. Invert Neurosci: 1-15.
  2. ^ Paula Sackmann, Mauricio Rabinovich and Juan Carlos Corley J. Econ. Entomol. (2001). "Successful Removal of German Yellowjackets (Hymenoptera: Vespidae) by Toxic Baiting." (PDF). pp. 94(4):811–816. http://anterior.inta.gov.ar/bariloche/ssd/nqn/ecologiadeinsectos/pdfs/Sackmann%20et%20al%202001.pdf. 
  3. ^ United States Environmental Protection Agency Office of Prevention, Pesticides and Toxic Substances (1996). "Fipronil. May 1996. New Pesticide Fact Sheet. US EPA Office of Prevention, Pesticides and Toxic Substances.". 
  4. ^ Ramesh C. Gupta (2007). Veterinary Toxicology. pp. 502–503. ISBN 9780123704672. http://books.google.com/?id=NgMX__L3q40C&pg=PA503&lpg=PA503&dq=fipronil+bioaccumulate+dogs. 
  5. ^ Mohamed F, Senarathna L, Percy A, Abeyewardene M, Eaglesham G, Cheng R, Azher S, Hittarage A, Dissanayake W, Sheriff MH, Davies W, Buckley NA, Eddleston M., Acute human self-poisoning with the N-phenylpyrazole insecticide fipronil--a GABAA-gated chloride channel blocker, J Toxicol Clin Toxicol. 2004;42(7):955-63).
  6. ^ Elise Kissling, BASF SE (2003). "BASF statement regarding temporary suspension of sales of crop protection products containing fipronil in France". http://www.agro.basf.com/agr/AP-Internet/en/content/news_room/news/basf-fipronil-temporary-suspension-in-france-statement. 
  7. ^ June 2000 BBC News story "Anti-locust drive 'created havoc'".
  8. ^ a b c d "Fipronil". Pesticides News 48: 20. 2000. 
  9. ^ "Frontline Plus Flea Treatment". http://www.frontlineplusonline.net/flea.php. Retrieved 2010-05-03. 
  10. ^ "Ecotoxicity for Fipronil". http://www.pesticideinfo.org/Detail_Chemical.jsp?Rec_Id=PC35768#Ecotoxicity. Retrieved 2010-05-03. 
  11. ^ "Colony Collapse Disorder linked to Fipronil". http://revistagloborural.globo.com/GloboRural/0,6993,EEC1707683-5809,00.html. Retrieved 2010-06-17. 
  12. ^ a b "Health and Environmental Aspects of Fipronil (TERMIDOR) Use in Tree Termite Eradication". http://www.flaes.org/pdf/Fipronil_FAQ%2003-03-03.pdf. Retrieved 2010-05-03. 

External links