Active ingredient |
Triasulfuron |
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Chemical name |
2-(2-chloroethoxy)-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzenesulfonamide |
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Classification |
Herbicide / Agrochemical |
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Formulation |
20%WDG, 75%WDG, 75%WP |
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Biochemistry |
Branched chain amino acid synthesis (ALS or AHAS) inhibitor. Acts by inhibiting biosynthesis of the essential amino acids valine and isoleucine, hence stopping cell division and plant growth. Selectivity derives from rapid metabolism in the crop. |
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Mode of action |
Selective herbicide, absorbed by the leaves and roots, and rapidly translocated to meristems. |
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Usage |
Control of broad-leaved weeds pre- and post-emergence in wheat, barley and triticale, at 5-10 g/ha. |
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Mammalian Toxicology |
Oral: Acute oral LD50 for rats and mice >5000 mg/kg. Skin and eye: Acute percutaneous LD50 for rats >2000 mg/kg. Mild skin irritant; non-irritating to eyes (rabbits). Non-sensitising to skin (guinea pigs). Inhalation: LC50 (4 h) for rats >5.18 mg/l air. |
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Certificate of quality |
Triasulfuron 95% Tech |
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Triasulfuron 20%WDG | ||||||||||||||
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