Fenpropathrin

Fenpropathrin
Identifiers
	IUPAC name [Cyano-(3-phenoxyphenyl)methyl] 2,2,3,3-tetramethylcyclopropane-1-carboxylate;
CAS Number	39515-41-8;
PubChem CID	47326;
ChemSpider	45352;
UNII	87BH96P0MX;
CompTox Dashboard (EPA)	DTXSID0024002 ;
ECHA InfoCard	100.049.514
Chemical and physical data
Formula	C22H23NO3
Molar mass	349.42292 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC1(C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C;
	InChI InChI=InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3; Key:XQUXKZZNEFRCAW-UHFFFAOYSA-N;

Fenpropathrin (brand names Danitol, Meothrin), or fenopropathrin, is a widely used pyrethroid insecticide in agriculture and household.[1][2][3][4]

A person developed Parkinson's disease after six months of daily exposure to fenpropathrin, and animal tests subsequently revealed that the compound is a dopaminergic neurotoxin.[4] It has thus been implicated as an environmental risk factor for Parkinson's disease.[4]

References

Hiroyasu Aizawa (2 December 2012). Metabolic Maps of Pesticides. Elsevier Science. pp. 185–. ISBN 978-0-323-15753-7.
Mohamed B. Abou-Donia (15 July 1992). Neurotoxicology. CRC Press. pp. 462–. ISBN 978-1-4398-0542-8.
Carl A. Johansen; Daniel F. Mayer (1990). Pollinator Protection: A Bee & Pesticide Handbook. Wicwas Press. ISBN 978-1-878075-00-0.
Xiong, Jing; Zhang, Xiaowei; Huang, Jinsha; Chen, Chunnuan; Chen, Zhenzhen; Liu, Ling; Zhang, Guoxin; Yang, Jiaolong; Zhang, Zhentao; Zhang, Zhaohui; Lin, Zhicheng; Xiong, Nian; Wang, Tao (2015). "Fenpropathrin, a Widely Used Pesticide, Causes Dopaminergic Degeneration". Molecular Neurobiology. 53 (2): 995–1008. doi:10.1007/s12035-014-9057-2. ISSN 0893-7648. PMC 5333774.

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[Aizawa2012-1] Hiroyasu Aizawa (2 December 2012). Metabolic Maps of Pesticides. Elsevier Science. pp. 185–. ISBN 978-0-323-15753-7.

[Abou-Donia1992-2] Mohamed B. Abou-Donia (15 July 1992). Neurotoxicology. CRC Press. pp. 462–. ISBN 978-1-4398-0542-8.

[JohansenMayer1990-3] Carl A. Johansen; Daniel F. Mayer (1990). Pollinator Protection: A Bee & Pesticide Handbook. Wicwas Press. ISBN 978-1-878075-00-0.

[XiongZhang2015-4] Xiong, Jing; Zhang, Xiaowei; Huang, Jinsha; Chen, Chunnuan; Chen, Zhenzhen; Liu, Ling; Zhang, Guoxin; Yang, Jiaolong; Zhang, Zhentao; Zhang, Zhaohui; Lin, Zhicheng; Xiong, Nian; Wang, Tao (2015). "Fenpropathrin, a Widely Used Pesticide, Causes Dopaminergic Degeneration". Molecular Neurobiology. 53 (2): 995–1008. doi:10.1007/s12035-014-9057-2. ISSN 0893-7648. PMC 5333774.

Pesticides
Pesticide types	Acaricide Bactericide Biocide Bioherbicide Biopesticide Fungicide Herbicide Insecticide Molluscicide Nematicide Piscicide Rodenticide Slimicide
Related topics	Health effects Environmental effects Fumigation Agricultural spray adjuvant Biological pest control Gene silencing Green pest management Integrated pest management Maximum residue limit Non-pesticide management Persistent organic pollutant Pest control Application Drift Formulation Degradation Misuse Paradox of the pesticides Poisoning Research Residue Resistance Bee toxicity Restricted use Pesticide Action Network Silent Spring The Pesticide Question Toxicity Class
By country	Canada European Union New Zealand United States
Integrated Pest Management Index of pesticide articles Pesticide categories

Monoamine neurotoxins
Adrenergic	DSP-4 Oxidopamine (6-OHDA)
Dopaminergic	Fenpropathrin Methamphetamine MPP⁺ MPTP Norsalsolinol Oxidopamine (6-OHDA) Rotenone
Serotonergic	3-CA 4-CAB 5,7-DHT α-Me-DA (3,4-DHA) αET αMT DCA MDA (tenamfetamine) MDMA (midomafetamine) PBA PCA PIA
See also: Receptor/signaling modulators • Adrenergics • Dopaminergics • Melatonergics • Serotonergics • Monoamine reuptake inhibitors • Monoamine releasing agents • Monoamine metabolism modulators

Fenpropathrin

See also

References