| Names | |
|---|---|
| Preferred IUPAC name N-{[(2Z)-But-2-en-1-yloxy]methyl}-2-chloro-N-(2,6-diethylphenyl)acetamide | |
Other names
| |
| Identifiers | |
3D model (JSmol) | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C17H24ClNO2 | |
| Molar mass | 309.83 g·mol−1 |
| Appearance | Pale yellow liquid [1] |
| Density | 1.10 kg/L (11 lb/imp. gal) [1] |
| Melting point | 12.9 °C (55.2 °F; 286.0 K) [1] |
| Boiling point | 167 °C (333 °F; 440 K) [1] |
| 29 mg/L [1] | |
| Vapor pressure | 0.93 mPa (0.02 mpsf) [1] |
| Hazards | |
| GHS labelling: [1] | |
| H302, H410 | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) | |
LC50 (median concentration) | 3.34 mg/L (rat, breathing) [1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Butenachlor is an obsolete selective chloroacetanilide, chloroacetamide herbicide used to control grasses and broadleaf weeds. [3] [4] It was introduced in 1976 and marketed as "Diphenox", [1] by Agro-Kanesho. [5]
Butenachlor's mode of action is to prevent formation of very long chain fatty acids; this makes its HRAC classification Group J (Australia), Group K3 (global) and Group 15 (numeric). [6]
Butenachlor doesn't persist in soil; its soil half-life is 2 to 5 days. It is moderately toxic to fish, with a 96-hour LC50 of 0.48 mg/L (0.034 gr/imp. gal). [1]