Fipronil
2D chemical structure of fipronil
3D chemical structure of fipronil
Names
Preferred IUPAC name
5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfinyl)pyrazole-3-carbonitrile[1]
Other names
Fipronil
Fluocyanobenpyrazole
Taurus
Termidor
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.102.312
KEGG
UNII
  • InChI=1S/C12H4Cl2F6N4OS/c13-5-1-4(11(15,16)17)2-6(14)8(5)24-10(22)9(7(3-21)23-24)26(25)12(18,19)20/h1-2H,22H2 checkY
    Key: ZOCSXAVNDGMNBV-UHFFFAOYSA-N checkY
  • InChI=1/C12H4Cl2F6N4OS/c13-5-1-4(11(15,16)17)2-6(14)8(5)24-10(22)9(7(3-21)23-24)26(25)12(18,19)20/h1-2H,22H2
    Key: ZOCSXAVNDGMNBV-UHFFFAOYAP
  • FC(F)(F)S(=O)c2c(C#N)nn(c1c(Cl)cc(cc1Cl)C(F)(F)F)c2N
Properties
C12H4Cl2F6N4OS
Molar mass 437.14 g·mol−1
Density 1.477-1.626 g/cm3
Melting point 200.5 °C (392.9 °F; 473.6 K)
Pharmacology
QP53AX15 (WHO)
Hazards
GHS labelling:
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
NFPA 704 (fire diamond)
[2]
NFPA 704 four-colored diamond
2
1
0
Lethal dose or concentration (LD, LC):
97 mg/kg (rat, oral)
0.25 mg/L (rainbow trout, aquatic)
Safety data sheet (SDS) Fipronil
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Fipronil is a broad-spectrum insecticide that belongs to the phenylpyrazole chemical family. Fipronil disrupts the insect central nervous system by blocking the ligand-gated ion channel of the GABAA receptor and glutamate-gated chloride (GluCl) channels. This causes hyperexcitation of contaminated insects' nerves and muscles. Fipronil's specificity towards insects is believed to be due to its greater binding affinity for the GABAA receptors of insects than to those of mammals, and for its action on GluCl channels, which do not exist in mammals.[3] As of 2017, there does not appear to be significant resistance among fleas to fipronil.[4]

Because of its effectiveness on various pests, fipronil is used as the active ingredient in flea control products for pets and home roach baits as well as field pest control for corn, golf courses, and commercial turf. Its widespread use makes its specific effects the subject of considerable attention. Observations on possible harm to humans or ecosystems are ongoing as well as the monitoring of pesticide resistance development.[5]

Physical properties

Fipronil (IUPAC name 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfinyl)pyrazole-3-carbonitrile[1]) is a white, solid powder with a moldy odor. It is degraded slightly by sunlight, stable at normal temperatures for one year, and is not stable in presence of metal ions.[6]

Use

Fipronil is/was used against many different pests on different crops, it is used against major lepidopteran (moth, butterfly, etc.) and orthopteran (grasshopper, locust, etc.) pests on a range of field and horticultural crops and against coleopteran (beetle) larvae in soils. it is employed for cockroach and ant control as well as locust control and termite pest control. In the United States of America, fipronil was approved for use against the Rasberry crazy ant until 2022[7] in counties of Texas where positive identification had been made by entomologists from the Texas Department of Agriculture and the Environmental Protection Agency. In New Zealand, fipronil was used in trials to control wasps (Vespula spp.), which are a threat to indigenous biodiversity.[8] It is now being used by the Department of Conservation to attempt local eradication of wasps,[9][10][11] and is being recommended for control of the invasive Argentine ant.[12] Fipronil is also the active ingredient in many commercial tick and flea treatments for pets.[13]

Effects

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 hours exposure and toxicity is considered to be low. It has been found to be very toxic to rabbits.[14]

The photodegradate MB46513 or desulfinylfipronil, appears to have a higher acute toxicity to mammals than fipronil itself by a factor of about 10.[15]

Symptoms of acute toxicity via ingestion includes sweating, nausea, vomiting, headache, abdominal pain, dizziness, agitation, weakness, and tonic-clonic seizures. Clinical signs of exposure to fipronil are generally reversible and resolve spontaneously. As of 2011, no data were available regarding the chronic effects of fipronil on humans. The United States Environmental Protection Agency has classified fipronil as a group C (possible human) carcinogen based on an increase in thyroid follicular cell tumors in both sexes of the rat. However, as of 2011, no human data are available regarding the carcinogenic effects of fipronil.[16]

Two Frontline TopSpot 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 veterinary physicians 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.[17] Fipronil is not volatile, so the likelihood of humans being exposed to this compound in the air is low.[16]

In contrast to neonicotinoids such as acetamiprid, clothianidin, imidacloprid, and thiamethoxam, which are absorbed through the skin to some extent, fipronil is not absorbed substantially through the skin.[18]

Drinking water contamination

In 2021, the US EPA put fipronil on the Draft Fifth Contaminant Candidate List (CCL 5) which can lead to future regulation under the Safe Drinking Water Act.[19]

Detection in body fluids

Fipronil may be quantitated in plasma by gas chromatography-mass spectrometry or liquid chromatography-mass spectrometry to confirm a diagnosis of poisoning in hospitalized patients or to provide evidence in a medicolegal death investigation.[20]

Ecological toxicity

Fipronil is highly toxic to crustaceans, insects (including bees and termites) and zooplankton, as well as 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.

Its half-life in soil is four months to one year, but much less on the soil surface because it is more sensitive to light (photolysis) than water (hydrolysis).[21]

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.[22] Also, adverse effects were indicated in the short term on several other invertebrate groups, one species of lizard (Trachylepis 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 the ecology of the habitat remain unknown, but appear unlikely to be severe.[17] Unfortunately, this lack of severity was not observed in bee species in South America. Fipronil is also used in Brazil and studies on the stingless bee Scaptotrigona postica have shown adverse reactions to the pesticide, including seizures, paralysis, and death with a lethal dose of .54 ng a.i./bee and a lethal concentration of .24 ng a.i./μl diet. These values are highly toxic in Scaptotrigona postica and bees in general.[23] Toxic baiting with fipronil has been shown to be effective in locally eliminating German wasps. All colonies within foraging range were eliminated within one week.[24][25]

In May 2003, the French Directorate-General of Food at the Ministry of Agriculture determined that a case of mass bee mortality observed in southern France was related to acute fipronil toxicity. Toxicity was linked to defective seed treatment, which generated dust. In February 2003, the ministry decided to temporarily suspend the sale of BASF crop protection products containing fipronil in France.[26] The seed treatment involved has since been banned.

Notable results from wildlife studies include:

  • Fipronil is highly toxic to fish and aquatic invertebrates. Its tendency to bind to sediments and its low water solubility may reduce the potential hazard to aquatic wildlife.[27]
  • Fipronil is toxic to bees and should not be applied to vegetation when bees are foraging.[27]
  • Based on ecological effects, fipronil is highly toxic to upland game birds on an acute oral basis and very highly toxic on a subacute dietary basis, but is practically nontoxic to waterfowl on both acute and subacute bases.[6]
  • Chronic (avian reproduction) studies show no effects at the highest levels tested in mallards (NOEC = 1000 ppm) or quail (NOEC = 10 ppm). The metabolite MB 46136 is more toxic than the parent to avian species tested (very highly toxic to upland game birds and moderately toxic to waterfowl on an acute oral basis).[6]
  • Fipronil is highly toxic to bluegill sunfish and highly toxic to rainbow trout on an acute basis.[6]
  • An early-lifestage toxicity study in rainbow trout found that fipronil affects larval growth with a NOEC of 0.0066 ppm and an LOEC of 0.015 ppm. The metabolite MB 46136 is more toxic than the parent to freshwater fish (6.3 times more toxic to rainbow trout and 3.3 times more toxic to bluegill sunfish). Based on an acute daphnia study using fipronil and three supplemental studies using its metabolites, fipronil is characterized as highly toxic to aquatic invertebrates.[6]
  • An invertebrate lifecycle daphnia study showed that fipronil affects length in daphnids at concentrations greater than 9.8 ppb.[6]
  • A lifecycle study in mysids shows fipronil affects reproduction, survival, and growth of mysids at concentrations less than 5 ppt.[6]
  • Acute studies of estuarine animals using oysters, mysids, and sheepshead minnows show that fipronil is highly acutely toxic to oysters and sheepshead minnows, and very highly toxic to mysids. Metabolites MB 46136 and MB 45950 are more toxic than the parent to freshwater invertebrates (MB 46136 is 6.6 times more toxic and MB 45950 is 1.9 times more toxic to freshwater invertebrates).[6]

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.[28] A synergistic toxic effect of fipronil with the fungal pathogen Nosema ceranae was recently reported.[29] The functional basis for this toxic effect is now understood: the synergy between fipronil and the pathogenic fungus induces changes in male bee physiology leading to infertility.[30] A 2013 report by the European Food Safety Authority identified fipronil as "a high acute risk to honeybees when used as a seed treatment for maize" and on July 16, 2013, the EU voted to ban the use of fipronil on maize and sunflowers within the EU. The ban took effect at the end of 2013.[31][32]

Pharmacodynamics

Fipronil acts by binding to allosteric sites of GABAA receptors and GluCl receptors (of insects) as an antagonist (a form of noncompetitive inhibition). This prevents the opening of chloride ion channels normally encouraged by GABA, reducing the chloride ions' ability to lower a neuron's membrane potential. This results in an overabundance of neurons reaching action potential and likewise CNS toxicity via overstimulation.[33][34][35][36]

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

In mammals (including humans) fipronil overdose is characterized by vomiting, agitation, and seizures. Intravenous or intramuscular benzodiazepines are a useful antidote.[37][38]

History

Development

Fipronil was discovered and developed by Rhône-Poulenc between 1985 and 1987, and placed on the market in 1993 under the B2 U.S. Patent 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.

2017 fipronil eggs contamination

The 2017 fipronil eggs contamination is an incident in Europe and South Korea involving the spread of insecticide contaminated eggs and egg products. Chicken eggs were found to contain fipronil and distributed to 15 European Union countries, Switzerland, and Hong Kong.[39][40] Approximately 700,000 eggs are thought to have reached shelves in the UK alone.[41] Eggs at 44 farms in Taiwan were also found with excessive fipronil levels.[42]

See also

References

  1. 1 2 "Compound Summary | 5-Amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile". PubChem. Bethesda, Md.: National Library of Medicine. n.d.
  2. ↑ "Safety Date Sheet" (PDF). Santa Cruz Biotechnology, Inc. 23 April 2019. SC-201546 - Fipronil. Retrieved 30 October 2023.
  3. ↑ Raymond-Delpech, Valérie; Matsuda, Kazuhiko; Sattelle, Benedict M.; Rauh, James J.; Sattelle, David B. (2005). "Ion channels: molecular targets of neuroactive insecticides". Invertebrate Neuroscience. 5 (3–4): 119–133. doi:10.1007/s10158-005-0004-9. ISSN 1354-2516. PMID 16172884. S2CID 12654353.
  4. ↑ Todd-Jenkins, Karen (18 June 2017). "Perception Versus Reality: Insecticide Resistance in Fleas". American Veterinarian. 2 (3). Archived from the original on 11 April 2020.{{cite journal}}: CS1 maint: unfit URL (link)
  5. ↑ Maddison, Jill E.; Page, Stephen W. (2008). Small Animal Clinical Pharmacology (2nd ed.). Elsevier Health Sciences. p. 229. ISBN 978-0-7020-2858-8.
  6. 1 2 3 4 5 6 7 8 "New Pesticide Fact Sheet". Office of Pesticide Programs; Office of Prevention, Pesticides, and Toxic Substances; United States Environmental Protection Agency. May 1996. EPA-737-F-96-005. Retrieved 30 October 2023 – via nepis.epa.gov.
  7. ↑ Keigwin, Richard C. Jr. (6 May 2019). "Quarantine exemption under the provisions of Section 18 of the Federal Insecticide, Fungicide and Rodenticide Act" (PDF). Letter to Texas Department of Agriculture. United States Environmental Protection Agency. Retrieved 30 October 2023 – via Texasagriculture.gov.
  8. ↑ "Wasp Warfare" (PDF). Revive Rotoiti. No. 24. St Arnaud: Department of Conservation; New Zealand Government. Autumn 2011. p. 2. Retrieved 30 October 2011.
  9. ↑ Neal, Tracy (10 February 2016). "War on wasps in Abel Tasman". RNZ. Radio New Zealand. Retrieved 30 October 2023.
  10. ↑ "Vespex: Making wide-area wasp control a reality - WWF's Conservation Innovation Awards". wwf-nz.crowdicity.com.
  11. ↑ "Wasp control Using Vespex". Department of Conservation; New Zealand Government. n.d. Retrieved 30 October 2023.
  12. ↑ "Argentine Ants". Department of Conservation; New Zealand Government. n.d. Retrieved 30 October 2023.
  13. ↑ "Vet Strength Flea & Tick Treatments for Cats & Dogs | FRONTLINE". uk.frontline.com. Retrieved 26 June 2023.
  14. ↑ "Fipronil Toxicity: Keep Flea Products Away from Rabbits". Veterinary Medicine at Illinois. Retrieved 20 November 2023.
  15. ↑ Hainzl, D.; Casida, J. E. (1996). "Fipronil insecticide: Novel photochemical desulfinylation with retention of neurotoxicity". Proceedings of the National Academy of Sciences. 93 (23): 12764–12767. Bibcode:1996PNAS...9312764H. doi:10.1073/pnas.93.23.12764. PMC 23994. PMID 8917493.
  16. 1 2 Jackson, D.; Cornell, C. B.; Luukinen, B.; Buhl, K.; Stone, D. (2009). "Fipronil Technical Fact Sheet". National Pesticide Information Center, Oregon State University Extension Services. Retrieved 30 October 2023.
  17. 1 2 "Fipronil". Pesticides News. Vol. 48. London: Pesticides Trust. 2000. p. 20. ISSN 0967-6597.
  18. ↑ "Cockroach Control". Pesticideresearch.com. 31 March 2013. Retrieved 10 August 2016.
  19. ↑ "Contaminant Candidate List 5 – CCL 5". United States Environmental Protection Agency. n.d. Retrieved 30 October 2023.
  20. ↑ Baselt, Randall C. (2017). Disposition of Toxic Drugs and Chemicals in Man (Eleventh ed.). Seal Beach, California: Biomedical Publications. pp. 894–895. ISBN 978-0-692-77499-1.
  21. ↑ Gunasekara, Amrith S.; Truong, Tresca; Goh, Kean S.; Spurlock, Frank; Tjeerdema, Ronald S. (2007). "Environmental fate and toxicology of fipronil" (PDF). Journal of Pesticide Science. 32 (3): 189–199. doi:10.1584/jpestics.R07-02. ISSN 1349-0923. Retrieved 30 October 2023.
  22. ↑ Kirby, Alex (27 June 2000). "Anti-locust drive 'created havoc'". Sci/Tech. BBC News. Retrieved 30 October 2023.
  23. ↑ Jacob, Cynthia Renata Oliveira; Soares, Hellen Maria; Carvalho, Stephan Malfitano; Nocelli, Roberta Cornélio Ferreira; Malaspina, Osmar (2013). "Acute Toxicity of Fipronil to the Stingless Bee Scaptotrigona postica Latreille". Bulletin of Environmental Contamination and Toxicology. 90 (1): 69–72. doi:10.1007/s00128-012-0892-4. ISSN 1432-0800. PMID 23179165. S2CID 35297535.
  24. ↑ Sackmann, Paula; Rabinovich, Mauricio; Corley, Juan Carlos (2001). "Successful Removal of German Yellowjackets (Hymenoptera: Vespidae) by Toxic Baiting". Journal of Economic Entomology. 94 (4): 811–816. doi:10.1603/0022-0493-94.4.811. ISSN 1938-291X. PMID 11561837.
  25. ↑ Hanna, Cause; Foote, David; Kremen, Claire (2012). "Short and long-term control of Vespula pensylvanica in Hawaii by fipronil baiting". Pest Management Science. 68 (7): 1026–1033. doi:10.1002/ps.3262. PMID 22392920.
  26. ↑ Kissling, Elise; BASF SE (2003). "BASF statement regarding temporary suspension of sales of crop protection products containing fipronil in France" (Press release).
  27. 1 2 "Fipronil" (PDF). National Pesticide Telecommunications Network; Oregon State University. n.d. p. 3. Retrieved 30 October 2023 – via Livingwithbugs.com.
  28. ↑ Lima, Pedro (n.d.). "Abelhas com microchip". Globo Rural (in Portuguese). Archived from the original on 12 January 2010.
  29. ↑ Aufauvre, Julie; Biron, David G.; Vidau, Cyril; et al. (2012). "Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee". Scientific Reports. 2. doi:10.1038/srep00326. PMC 3310228. PMID 22442753. Article number: 326.
  30. ↑ Kairo, Guillaume; Biron, David G.; Ben Abdelkader, Faten; et al. (2017). "Nosema ceranae, Fipronil and their combination compromise honey bee reproduction via changes in male physiology". Scientific Reports. 7. doi:10.1038/s41598-017-08380-5. PMC 5561069. PMID 28819220. Article number: 8556.
  31. ↑ "EFSA assesses risks to bees from fipronil" (Press release). European Food Safety Authority. 27 May 2013. Retrieved 30 October 2023.
  32. ↑ Carrington, Damian (16 July 2013). "EU to ban fipronil to protect honeybees". The Guardian. London.
  33. ↑ Cole, L. M.; Nicholson, R. A.; Casida, J. E. (1993). "Action of Phenylpyrazole Insecticides at the GABA-Gated Chloride Channel". Pesticide Biochemistry and Physiology. 46: 47–54. doi:10.1006/pest.1993.1035.
  34. ↑ Ratra, G. S.; Casida, J. E. (2001). "GABA receptor subunit composition relative to insecticide potency and selectivity". Toxicol. Lett. 122 (3): 215–222. doi:10.1016/s0378-4274(01)00366-6. PMID 11489356.
  35. ↑ Olsen, Richard W.; DeLorey, Timothy M. (1999). "GABA Receptor Physiology and Pharmacology". In Siegel, G. J.; Agranoff, B. W.; Fisher, S. K.; Albers, R. W.; Uhler, M. D. (eds.). Basic Neurochemistry: Molecular, Cellular and Medical Aspects (6th ed.). Philadelphia: Lippincott-Raven. ISBN 978-0-397-51820-3.
  36. ↑ "4.15 Fipronil (T)*". Pesticide Residues in Food – 1997: Report of the Joint Meeting of the FAO Panel of Experts on Pesticide Residues in Food and the Environment and the WHO Core Assessment Group on Pesticide Residues: Lyons, France: 22 September - 1 October 1997, Part 1. FAO Plant Production and Protection Paper 145. Rome: Food and Agriculture Organization of the United Nations; World Health Organization. 1998. ISBN 978-92-5-104116-1. ISSN 0259-2517. M-84.
  37. ↑ Gupta, Ramesh C. (2007). Veterinary Toxicology: Basic and Clinical Principles. New York: Academic Press. pp. 502–503. ISBN 978-0-12-370467-2.
  38. ↑ Mohamed, Fahim; Senarathna, Lalith; Percy, Adrian; et al. (2004). "Acute Human Self‐Poisoning with the N ‐Phenylpyrazole Insecticide Fipronil—a GABA A ‐Gated Chloride Channel Blocker". Journal of Toxicology: Clinical Toxicology. 42 (7): 955–963. doi:10.1081/clt-200041784. PMC 1351141. PMID 15641641.
  39. ↑ "Eggs containing fipronil found in 15 EU countries and Hong Kong". BBC News. 11 August 2017. Retrieved 30 October 2023.
  40. ↑ "EU: 17 nations get tainted eggs, products in growing scandal". ABC News. Associated Press. Archived from the original on 11 August 2017.
  41. ↑ Boffey, Daniel (11 August 2017). "Egg contamination scandal widens as 15 EU states, Switzerland and Hong Kong affected". The Guardian. Retrieved 11 August 2017.
  42. ↑ "Eggs at 44 farms in Taiwan found with excessive insecticide levels". Taiwan News. 26 August 2017. Retrieved 26 August 2017.
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