| Names | |
|---|---|
| IUPAC name N-[dimethylamino(fluoro)phosphoryl]-N-methylmethanamine | |
| Other names | |
| Identifiers | |
| |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider |
|
| ECHA InfoCard | 100.003.706 |
| EC Number |
|
| KEGG |
|
| UNII | |
| |
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| Properties | |
| C4H12FN2OP | |
| Molar mass | 154.125 g·mol−1 |
| Appearance | colourless liquid |
| Density | 1.11 g·mL–1 |
| 14.8 g·L–1 | |
| Vapor pressure | 14663 mPa |
Henry's law constant (kH) | 2.28·10–8 atm·m3·mol–1[2] |
| Pharmacology | |
| inhalation and dermal contact | |
| Legal status | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards | Highly Toxic |
| GHS labelling: | |
| Danger | |
| H300,H310 | |
| 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 (intravenous, rabbits)[1] |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Dimefox, also known asTL-792 orT-2002, is a highly toxicorganophosphateinsecticide. In its pure form it is a colourless liquid with a fishy odour.[3] Dimefox was first produced in 1940 by the group ofGerhard Schrader in Germany. It was historically used as a pesticide, but has been deemed obsolete or discontinued for use by theWorld Health Organization. It is not guaranteed that all commercial use of this compound ceased, but in most countries[which?] it is no longer registered for use as a pesticide.[4] It is considered anextremely hazardous substance as defined by the United StatesEmergency Planning and Community Right-to-Know Act.
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