Oral Acute oral LD50 for male rats 3738, female rats 2675 mg/kg. Skin and eye Acute percutaneous LD50 for rabbits >2000 mg/kg; a
severe eye irritant, not a skin irritant. Inhalation LC50 (4 h) for rats >0.38 mg/l. NOEL (2 y) for rats 15, male mice 500, female
mice >2000 mg/kg b.w. daily. ADI 0.15 mg/kg. Other Non-carcinogenic, non-mutagenic, non-teratogenic, and produces no significant
toxicological effects on reproductive parameters. Toxicity class WHO (a.i.) U; EPA (formulation) IV EC classification Xi; R41| N;
R51, R53

Clopyralid Mode of action Selective systemic herbicide, absorbed by the leaves and roots, with translocation both acropetally and
basipetally, and accumulation in meristematic tissue. Exhibits an auxin-type reaction. Acts on cell elongation and respiration.
clopyralid uses: Post-emergence control of many annual and perennial broad-leaved weeds of the families Polygonaceae, Compositae,
Leguminosae, and Umbelliferae, in sugar beet, fodder beet, oilseed rape, maize, cereals, brassicas, onions, leeks, strawberries
and flax (at 70-300 g a.e./ha), and in grassland and non-crop land (at 300-560 g a.e./ha). Provides particularly good control of
creeping thistle (Cirsium arvense), perennial sow-thistle, coltsfoot, mayweeds, and Polygonum spp. Phytotoxicity Good crop
tolerance of graminaceous, cruciferous and chenopodiaceous crops. Clopyralid Formulation types SG; SL.

2000L