Esfenvalerate
Names | |
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Preferred IUPAC name (S)-Cyano(3-phenoxyphenyl)methyl (2S)-2-(4-chlorophenyl)-3-methylbutanoate | |
Other names Asana (S)-Fenvalerate | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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Beilstein Reference | 4275674 |
ChEBI |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.118.804 |
EC Number |
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KEGG |
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PubChem CID |
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UNII |
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UN number | 3349 |
CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C25H22ClNO3 |
Molar mass | 419.91 g·mol−1 |
Density | 1.211 g/cm3 |
Melting point | 60 °C (140 °F; 333 K) |
log P | 6.22 |
Vapor pressure | 0 mmHg at 25 °C |
Hazards | |
GHS labelling: | |
Pictograms | |
Danger | |
H301, H313, H316, H317, H320, H330, H335, H370, H373, H410 | |
P260, P261, P264, P270, P271, P272, P273, P280, P284, P301+P310, P302+P352, P304+P340, P305+P351+P338, P307+P311, P310, P312, P314, P320, P321, P330, P332+P313, P333+P313, P337+P313, P363, P391, P403+P233, P405, P501 | |
Flash point | 256 °C (493 °F; 529 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Esfenvalerate is a synthetic pyrethroid insecticide marketed under the brand Asana.[2] It is the (S)-enantiomer of fenvalerate.[3]
In the United States, a limit of .05 ppm of the chemical's residue is permissible in food.[4]
References
- ^ Kelly, Kevin. "Environmental Fate of Esfenvalerate". California Environmental Protection Agency. Retrieved January 10, 2013.
- ^ Fishel, Frederick M. (2012). "Pesticide Toxicity Profile: Synthetic Pyrethroid Pesticides". University of Florida. Archived from the original on May 12, 2016. Retrieved January 10, 2013.
- ^ "Esfenvalerate". EXTONET (Extension Toxicology Network). Cooperative Extension Offices of Cornell University, Michigan State University, Oregon State University, and University of California at Davis. May 1994. Retrieved January 10, 2013.
- ^ The Code of Federal Regulations of the United States of America. U.S. Government Printing Office. 2006. pp. 445–446.
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- Aluminium phosphide
- Boric acid
- Chromated copper arsenate
- Copper(II) arsenate
- Copper(I) cyanide
- Cryolite
- Diatomaceous earth
- Lead hydrogen arsenate
- Paris Green
- Scheele's Green
- Acephate
- Azamethiphos
- Azinphos-methyl
- Bensulide
- Chlorethoxyfos
- Chlorfenvinphos
- Chlorpyrifos
- Chlorpyrifos-methyl
- Coumaphos
- Demeton-S-methyl
- Diazinon
- Dichlorvos
- Dicrotophos
- Diisopropyl fluorophosphate
- Dimefox
- Dimethoate
- Dioxathion
- Disulfoton
- Ethion
- Ethoprop
- Fenamiphos
- Fenitrothion
- Fenthion
- Fosthiazate
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- Oxydemeton-methyl
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- Parathion-methyl
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- Phorate
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- Phosmet
- Phoxim
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- Quinalphos
- R-16661
- Schradan
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- Terbufos
- Tetrachlorvinphos
- Tribufos
- Trichlorfon
- Acrinathrin
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- Bifenthrin
- Bioallethrin
- Cyfluthrin
- Cyhalothrin
- Cypermethrin
- Cyphenothrin
- Deltamethrin
- Empenthrin
- Esfenvalerate
- Etofenprox
- Fenpropathrin
- Fenvalerate
- Flumethrin
- Fluvalinate
- Imiprothrin
- Metofluthrin
- Permethrin
- Phenothrin
- Prallethrin
- Pyrethrin (I, II; chrysanthemic acid)
- Pyrethrum
- Resmethrin
- Silafluofen
- Tefluthrin
- Tetramethrin
- Tralomethrin
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- Afoxolaner
- Amitraz
- Azadirachtin
- Bensultap
- Buprofezin
- Cartap
- Chlordimeform
- Chlorfenapyr
- Cyromazine
- Fenazaquin
- Fenoxycarb
- Fipronil
- Fluralaner
- Hydramethylnon
- Indoxacarb
- Limonene
- Lotilaner (+milbemycin oxime)
- Pyridaben
- Pyriprole
- Sarolaner
- Adjuvants (Piperonyl butoxide, Sesamex)
- Spinosad
- Sulfluramid
- Tebufenozide
- Tebufenpyrad
- Veracevine
- Xanthone
- Metaflumizone
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