Dimefox

Dimefox
Names
	IUPAC name N-[dimethylamino(fluoro)phosphoryl]-N-methylmethanamine
	Other names TL-792; T-2002
Identifiers
CAS Number	115-26-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:82119 ;
ChemSpider	7966 ;
ECHA InfoCard	100.003.706
EC Number	204-076-8;
KEGG	C18980 ;
PubChem CID	8264;
UNII	N8RU9F1IQD ;
CompTox Dashboard (EPA)	DTXSID8041870 ;
	InChI InChI=1S/C4H12FN2OP/c1-6(2)9(5,8)7(3)4/h1-4H3 Key: PGJBQBDNXAZHBP-UHFFFAOYSA-N ; InChI=1/C4H12FN2OP/c1-6(2)9(5,8)7(3)4/h1-4H3 Key: PGJBQBDNXAZHBP-UHFFFAOYAM;
	SMILES CN(C)P(=O)(N(C)C)F;
Properties
Chemical formula	C4H12FN2OP
Molar mass	154.125 g·mol−1
Appearance	colourless liquid
Density	1.11 g·mL–1
Solubility in water	1000000 mg·L–1
Vapor pressure	14663 mPa
Henry's law; constant (kH)	2.28·10–8 atm·m3·mol–1
Pharmacology
Routes of; administration	inhalation and dermal contact
Legal status	UK: Banned; US: Banned;
Hazards
Main hazards	Highly Toxic
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H300, H310
Precautionary statements	P262, P264, P270, P280, P301+P310, P302+P350, P310, P321, P322, P330, P361, P363, P405, P501
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	2 mg/kg (oral, mice); 1 mg/kg (oral, rats); 3 mg/kg (intrevenous, rabbits)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	(what is ?)
	Infobox references

Dimefox was an organophosphate pesticide. In its pure form it is a colourless liquid with a fishy odour.^[3] Dimefox was first produced in 1940 by the group of Gerhard Schrader in Germany. It was historically used as a pesticide, but has been deemed obsolete or discontinued for use by the World Health Organization. However, they do not guarantee that all commercial use of this compound ceased. But in most countries it is no longer registered for use as a pesticide.^[4] It is considered an extremely hazardous substance as defined by the United States Emergency Planning and Community Right-to-Know Act.

References[]

^ ^a ^b ^c ^d ^e Chemical Warfare Agents, and Related Chemical Problems. Parts I-II.
^ "Dimefox".
^ "Archived copy". Archived from the original on 2011-07-22. Retrieved 2011-04-06.CS1 maint: archived copy as title (link)
^ the WHO recommended classification of pesticides by hazard and guidelines to classification 2009, [1]

This article about an organic compound is a stub. You can help Wikipedia by .

[PB158508-1] Chemical Warfare Agents, and Related Chemical Problems. Parts I-II.

[PubChem-2] "Dimefox".

[IAI-3] "Archived copy". Archived from the original on 2011-07-22. Retrieved 2011-04-06.CS1 maint: archived copy as title (link)

[WHO-4] the WHO recommended classification of pesticides by hazard and guidelines to classification 2009, [1]

[1]

[2]

[3]

[4]

v t Pest control: Insecticides
Carbamates	Aldicarb Aminocarb Bendiocarb Butocarboxim Carbaryl Carbofuran Carbosulfan m-Cumenyl methylcarbamate Ethienocarb Fenobucarb Methomyl Metolcarb Oxamyl Promecarb Propoxur
Inorganic compounds	Aluminium phosphide Boric acid Chromated copper arsenate Copper(II) arsenate Copper(I) cyanide Cryolite 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 DFDT Dicofol Dieldrin Endosulfan Endrin Heptachlor Kepone Lindane Methoxychlor Mirex Tetradifon Toxaphene
Organophosphorus	Acephate Azamethiphos Azinphos-methyl Bensulide Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Coumaphos Demeton-S-methyl Diazinon Dichlorvos Dicrotophos Diisopropyl fluorophosphate Dimefox Dimethoate Dioxathion Disulfoton Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Isoxathion Malathion Methamidophos Methidathion Mevinphos Mipafox Monocrotophos Naled Omethoate Oxydemeton-methyl Parathion Parathion-methyl Phenthoate Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Quinalphos R-16661 Schradan Temefos Tebupirimfos Terbufos Tetrachlorvinphos 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
Other chemicals	Afoxolaner Amitraz Azadirachtin Bensultap Buprofezin Cartap Chlordimeform Chlorfenapyr Cyromazine Fenoxycarb Fipronil Fluralaner Hydramethylnon Indoxacarb Limonene Lotilaner (+milbemycin oxime) Pyriprole Sarolaner Sesamex Spinosad Tebufenozide Tebufenpyrad Veracevine Xanthone Metaflumizone
Metabolites	Oxon Malaoxon Paraoxon TCPy
Biopesticides	Bacillus thuringiensis Baculovirus Beauveria bassiana Isaria fumosorosea Metarhizium acridum Metarhizium anisopliae Nomuraea rileyi Lecanicillium lecanii Paenibacillus popilliae Purpureocillium lilacinum

v t Neurotoxins
	Batrachotoxin Bestoxin Birtoxin Bungarotoxin Charybdotoxin Conotoxin Fasciculin Huwentoxin Poneratoxin Saxitoxin Tetrodotoxin Vanillotoxin Spooky toxin (SsTx) Epibatidine Zetekitoxin AB Dendrotoxin
Bacterial	Botulinum toxin Tetanospasmin
Cyanotoxins	Anatoxin-a Guanitoxin BMAA Saxitoxin
Plant toxins	Bicuculline Penitrem A Picrotoxin Strychnine Tutin Rotenone Ginkgotoxin Cicutoxin Oenanthotoxin Thujone Volkensin
Mycotoxins	Ibotenic acid Muscarine Muscimol
Pesticides	Fenpropathrin Tetramethylenedisulfotetramine Bromethalin Crimidine Methamidophos Endosulfan Fipronil Phenylsilatrane Chlorophenylsilatrane Sulfuryl fluoride Mipafox Schradan Dimefox
Nerve agents	Cyclosarin EA-3148 Novichok agent Sarin Soman Tabun VE VG VM VP VR VX GV EA-3990 EA-4056 T-1123 Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide) Fluorotabun Chinese VX EA-2192
Bicyclic phosphates	TBPS TBPO IPTBO
Other	Dimethylcadmium Dimethylmercury Toxopyrimidine IDPN

Names


IUPAC name N-[dimethylamino(fluoro)phosphoryl]-N-methylmethanamine
Other names TL-792^[1] T-2002^[1]
Identifiers
CAS Number	115-26-4^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:82119^Y
ChemSpider	7966^Y
ECHA InfoCard	100.003.706
EC Number	204-076-8
KEGG	C18980^Y
PubChem CID	8264
UNII	N8RU9F1IQD^Y
CompTox Dashboard (EPA)	DTXSID8041870
InChI InChI=1S/C4H12FN2OP/c1-6(2)9(5,8)7(3)4/h1-4H3^N Key: PGJBQBDNXAZHBP-UHFFFAOYSA-N^N InChI=1/C4H12FN2OP/c1-6(2)9(5,8)7(3)4/h1-4H3 Key: PGJBQBDNXAZHBP-UHFFFAOYAM
SMILES CN(C)P(=O)(N(C)C)F
Properties
Chemical formula	C₄H₁₂FN₂OP
Molar mass	154.125 g·mol⁻¹
Appearance	colourless liquid
Density	1.11 g·mL^–1
Solubility in water	1000000 mg·L^–1
Vapor pressure	14663 mPa
Henry's law constant (k_H)	2.28·10^–8 atm·m³·mol^–1^[2]
Pharmacology
Routes of administration	inhalation and dermal contact
Legal status	UK: Banned US: Banned
Hazards
Main hazards	Highly Toxic
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H300, H310
Precautionary statements	P262, P264, P270, P280, P301+P310, P302+P350, P310, P321, P322, P330, P361, P363, P405, P501
Lethal dose or concentration (LD, LC):
LD₅₀ (median dose)	2 mg/kg (oral, mice)^[1] 1 mg/kg (oral, rats)^[1] 3 mg/kg (intrevenous, rabbits)^[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N (what is ^YN ?)
Infobox references

Dimefox

See also[]

References[]