Products >> Herbicides >> Pyrazosulfuron-ethyl
Pyrazosulfuron-ethyl 75%WDG
Herbicide
HRAC B WSSA 2; sulfonylurea
Pyrazosulfuron-ethyl NOMENCLATURE
Common name pyrazosulfuron-ethyl
IUPAC name ethyl 5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-1-methylpyrazole-4-carboxylate
Chemical Abstracts name ethyl 5-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrazole-4-carboxylate
CAS RN [93697-74-6] Development codes NC-311 (Nissan)
Pyrazosulfuron-ethyl APPLICATIONS
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 (demethylation of methoxy group) in
the crop. Metabolic basis of selectivity in sulfonylureas reviewed
(M. K. Koeppe & H. M. Brown, Agro-Food-Industry, 6, 9-14 (1995)).
Mode of action Systemic herbicide, absorbed by roots and/or leaves
and translocated to the meristems. Uses Control of annual and perennial
broad-leaved weeds and sedges, pre- or post-emergence in wet-sown
and transplanted rice crops, at 15-30 g/ha. Formulation types GR;
SC; WG; WP. Selected tradenames: 'Agreen' (Nissan); 'Sirius' (Nissan);
'Billy' (Sanonda); mixtures: 'Act' (+ mefenacet) (Nihon Bayer, Nissan,
Yashima); 'Kirifuda' (+ indanofan) (Mitsubishi Chemical); 'Regnet'
(+ indanofan) (Mitsubishi Chemical); 'Sparkstar G' (+ dimethametryn+
esprocarb+ pretilachlor) (Nissan, Syngenta)
Pyrazosulfuron-ethyl OTHER TRADENAMES
pyrazosulfuron-ethyl
'Acord' (Crystal) mixtures: 'Revolver' (+ cyhalofop-butyl+ mefenacet)
(Nissan); 'Staabo' (+ pentoxazone) (Kaken, Nissan); 'Starbo' (+
pentoxazone) (Nissan); 'Sunwell' (+ etobenzanid) (Hodogaya, Nissan);
'Agrostar' (+ butamifos+ cyhalofop-butyl) (Agros); 'Contract' (+
esprocarb) (Syngenta); 'Die-Hard' (+ cafenstrole) (Nissan, Shionogi,
Yashima); 'Grassy' (+ indanofan) (Mitsubishi Chemical); 'Nondoctor'
(+ indanofan) (Korea) (Mitsubishi Chemical); 'Pyrasulfonil' (+ propanil)
(Crystal); 'Striker' (+ cafenstrole+ cyhalofop-butyl) (Nissan, Yashima);
'Trebiace' (+ indanofan) (for turf) (Mitsubishi Chemical)
Pyrazosulfuron-ethyl ANALYSIS
Product by hplc. Methods for sulfonylurea residues in crops, soil
and water reviewed (A. C. Barefoot et al., Proc. Br. Crop Prot.
Conf. - Weeds, 1995, 2, 707). Details from Nissan.
MAMMALIAN TOXICOLOGY
Oral Acute oral LD50 for rats and mice >5000 mg/kg. Skin and
eye Acute percutaneous LD50 for rats >2000 mg/kg. Non-irritating
to skin and eyes (rabbits). Non-sensitising to skin (guinea pigs).
Inhalation LC50 for rats >3.9 mg/l air. NOEL (78 w) for mice
4.3 mg/kg daily. ADI 0.043 mg/kg. Other Non-mutagenic in the Ames
test. Non-teratogenic in rats and rabbits. Toxicity class WHO (a.i.)
III (Table 5)
Pyrazosulfuron-ethyl ECOTOXICOLOGY
pyrazosulfuron-ethyl
Birds Acute oral LD50 for bobwhite quail >2250 mg/kg. Fish LC50
(96 h) for rainbow trout and bluegill sunfish >180 mg/l; (48
h) for carp >30 mg/l. Daphnia TLm (3 h) >40 ppm. Algae I50
for green algae (Scenedesmus acutus) 1 ppm. Bees LD50 (contact)
>100 mg/bee.
ENVIRONMENTAL FATE
Animals In rats, after 48 h, 80% of applied pyrazosulfuron-ethyl
is excreted in urine and faeces. The major metabolic reaction is
demethylation of the methoxy group. Soil/Environment In soil, DT50
<15 d. In water, DT50 in buffer solution (pH 7), paddy fields
or river water are c. 28 d.