Tetramethrin

Tetramethrin
Names


IUPAC name (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
Identifiers
CAS Number	7696-12-0^Y
ChEBI	CHEBI:39397^Y
ChemSpider	75773^Y
EC Number	214-619-0
Jmol interactive 3D	Image
KEGG	D07368^Y
PubChem	83975
RTECS number	GZ1730000
UNII	Z72930Q46K^Y
InChI InChI=1S/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3^Y Key: CXBMCYHAMVGWJQ-UHFFFAOYSA-N^Y InChI=1/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3 Key: CXBMCYHAMVGWJQ-UHFFFAOYAA
SMILES O=C1\C3=C(/C(=O)N1COC(=O)C2C(\C=C(/C)C)C2(C)C)CCCC3
Properties
Chemical formula	C₁₉H₂₅NO₄
Molar mass	331.406 g/mol
Appearance	white crystalline solid
Odor	strong, pyrethrum-like
Density	1.108 g/cm³
Melting point	65 to 80 °C (149 to 176 °F; 338 to 353 K)
Solubility in water	0.00183 g/100 mL
Solubility	soluble in methane, hexane slightly soluble in acetone, n-octanol, ethanol very slightly soluble in xylene
log P	4.73
Vapor pressure	10 Pa
Refractive index (n_D)	1.5175
Pharmacology
ATC code	P03BA04 QP53AC13
Hazards
Lethal dose or concentration (LD, LC):
LD₅₀ (Median dose)	20,000 mg/kg (rat, oral)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is ^YN ?)
Infobox references

Tetramethrin is a potent synthetic insecticide in the pyrethroid family.^[1] It is a white crystalline solid with a melting point of 65-80 °C. The commercial product is a mixture of stereoisomers.

It is commonly used as an insecticide, and affects the insect's nervous system. It is found in many household insecticide products.^[2]

References

↑ Tetramethrin, alanwood.net
↑ Tetramethrin, Household Products Database

External links

Pyrethrins and Pyrethroids Fact Sheet - National Pesticide Information Center
Pyrethrins and Pyrethroids Pesticide Information Profile - Extension Toxicology Network
Tetramethrin in the Pesticide Properties DataBase (PPDB)

Pest control: insecticides

Carbamates	Aldicarb Bendiocarb Carbaryl Carbofuran Ethienocarb Fenobucarb Oxamyl Methomyl Propoxur

Inorganic compounds	Aluminium phosphide Boric acid Chromated copper arsenate Copper(II) arsenate Copper(I) cyanide Diatomaceous earth Lead hydrogen arsenate Paris Green Scheele's Green

Insect growth regulators	Benzoylureas Diflubenzuron Flufenoxuron Hydroprene Lufenuron Methoprene Pyriproxyfen

Neonicotinoids	Acetamiprid Clothianidin Dinotefuran Imidacloprid Nitenpyram Nithiazine Thiacloprid Thiamethoxam

Organochlorides	Aldrin Beta-HCH Carbon tetrachloride Chlordane Cyclodiene 1,2-DCB 1,4-DCB 1,1-DCE 1,2-DCE DDD DDE DDT Dicofol Dieldrin Endosulfan Endrin Heptachlor Kepone Lindane Methoxychlor Mirex Tetradifon Toxaphene

Organophosphorus	Acephate Azamethiphos Azinphos-methyl Bensulide Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Chlorpyrifos-methyl Coumaphos Demeton-S-methyl Diazinon Dicrotophos Diisopropyl fluorophosphate Dimethoate Dioxathion Disulfoton Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Fosthiazate Isoxathion Malathion Methamidophos Methidathion Mevinphos Monocrotophos Naled Omethoate Oxydemeton-methyl Parathion Parathion-methyl Phenthoate Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Quinalphos Temefos Tebupirimfos Terbufos Tetrachlorvinphos Tribufos Trichlorfon

Pyrethroids	Acrinathrin Allethrins Bifenthrin Bioallethrin Cyfluthrin Cyhalothrin Cypermethrin Cyphenothrin Deltamethrin Empenthrin Esfenvalerate Etofenprox Fenvalerate Flumethrin Imiprothrin Metofluthrin Permethrin Phenothrin Prallethrin Pyrethrin (I, II; chrysanthemic acid) Pyrethrum Resmethrin Silafluofen Tefluthrin Tetramethrin Tralomethrin Transfluthrin

Ryanoids	Chlorantraniliprole Cyantraniliprole Flubendiamide Ryanodine Ryanodol

Other chemicals	Amitraz Azadirachtin Chlordimeform Chlorfenapyr Cyromazine Fenazaquin Fenoxycarb Fipronil Hydramethylnon Indoxacarb Limonene Pyridaben Pyriprole Ryanodine Sesamex Spinosad Sulfluramid Tebufenozide Tebufenpyrad Veracevine Xanthone

Metabolites	Oxon Malaoxon Paraoxon TCPy

Biopesticides	Bacillus thuringiensis Baculovirus Beauveria bassiana Beauveria brongniartii Metarhizium acridum Metarhizium anisopliae Nomuraea rileyi Lecanicillium lecanii Paecilomyces fumosoroseus Paenibacillus popilliae Purpureocillium lilacinum

This article is issued from Wikipedia - version of the Monday, November 30, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.