Phosmet

Phosmet^[1]
Names
	IUPAC name 2-(Dimethoxyphosphinothioylthiomethyl)isoindoline-1,3-dione
	Other names Fosmet; Decemthion; Imidathion; Imidan; Phthalophos
Identifiers
CAS Number	732-11-6
3D model (Jmol)	Interactive image
ChEBI	CHEBI:38786
ChemSpider	12367
ECHA InfoCard	100.010.899
KEGG	C18756
PubChem	12901
UNII	VN04LI540Y
	InChI InChI=1S/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3 Key: LMNZTLDVJIUSHT-UHFFFAOYSA-N ; InChI=1/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3 Key: LMNZTLDVJIUSHT-UHFFFAOYAV ;
	SMILES O=C2c1ccccc1C(=O)N2CSP(=S)(OC)OC ;
Properties
Chemical formula	C11H12NO4PS2
Molar mass	317.323
Appearance	White to off-white crystals
Density	1.03 g/cm3
Melting point	72 °C (162 °F; 345 K)
Boiling point	Decomposes at >100 °C
Pharmacology
ATCvet code	QP53AF06 (WHO) QP53BB03 (WHO)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Phosmet is a phthalimide-derived, non-systemic, organophosphate insecticide used on plants and animals. It is mainly used on apple trees for control of codling moth, though it is also used on a wide range of fruit crops, ornamentals, and vines for the control of aphids, suckers, mites, and fruit flies.^[2]

Safety[edit]

Phosmet is on the US Emergency Planning List of Extremely Hazardous Substances. It is highly toxic to bees.^[2]

References[edit]

^ "Phosmet Safety Card". Retrieved 2006-08-06.
^ ^a ^b "Toxicology of Phosmet" (Webpage). Retrieved 2006-08-06.

External links[edit]

Phosmet in the Pesticide Properties DataBase (PPDB)

[safety-1] "Phosmet Safety Card". Retrieved 2006-08-06.

[Toxicology-2] "Toxicology of Phosmet" (Webpage). Retrieved 2006-08-06.

[1]

[2]

v t e 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 Fenpropathrin 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	Afoxolaner Amitraz Azadirachtin Buprofezin Chlordimeform Chlorfenapyr Cyromazine Fenazaquin Fenoxycarb Fipronil Fluralaner Hydramethylnon Indoxacarb Limonene Lotilaner Pyridaben Pyriprole Ryanodine Sarolaner Sesamex Spinosad Sulfluramid Tebufenozide Tebufenpyrad Veracevine Xanthone Metaflumizone

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

Phosmet

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References[edit]

External links[edit]

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Names


IUPAC name 2-(Dimethoxyphosphinothioylthiomethyl)isoindoline-1,3-dione
Other names Fosmet Decemthion Imidathion Imidan Phthalophos
Identifiers
CAS Number	732-11-6^Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:38786^Y
ChemSpider	12367^Y
ECHA InfoCard	100.010.899
KEGG	C18756^Y
PubChem	12901
UNII	VN04LI540Y^Y
InChI InChI=1S/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3^Y Key: LMNZTLDVJIUSHT-UHFFFAOYSA-N^Y InChI=1/C11H12NO4PS2/c1-15-17(18,16-2)19-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h3-6H,7H2,1-2H3 Key: LMNZTLDVJIUSHT-UHFFFAOYAV
SMILES O=C2c1ccccc1C(=O)N2CSP(=S)(OC)OC
Properties
Chemical formula	C₁₁H₁₂NO₄PS₂
Molar mass	317.323
Appearance	White to off-white crystals
Density	1.03 g/cm³
Melting point	72 °C (162 °F; 345 K)
Boiling point	Decomposes at >100 °C
Pharmacology
ATCvet code	QP53AF06 (WHO) QP53BB03 (WHO)
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