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Chemical Identification
Common Name
Rimsulfuron
中文通用名
砜嘧磺隆
IUPAC
1-(4,6-dimethoxypyrimidin-2-yl)-3-(3-ethylsulfonyl-2-pyridylsulfonyl)urea
CAS
N-[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]-3-(ethylsulfonyl)-2-pyridinesulfonamide
CAS No.
122931-48-0
Molecular Formula
C14H17N5O7S2
Molecular Structure
Category
Activity
Herbicide

Rimsulfuron is absorbed by the foliage of treated plants and translocated to the meristem. The site of action is acetolactate synthase (ALS), an enzyme in branched chain amino acid biosynthesis. The initial metabolic pathway for rimsulfuron in maize initially involves hydroxylation on the pyrimidine ring followed by glucose conjugation.

The optimum time for application varies. Generally, annual weeds require early post-emergence treatments (between two and five leaves) with annual grasses requiring treatment before tillering. Perennial weeds should be treated when taller and may benefit from sequential treatments. Adjuvants are essential for consistent weed control. A second application at up to the 6-8 leaf stage of maize is advised for the control of summer weeds. Post-emergence applications are most effective in tomatoes.

In field trials, rimsulfuron generally showed equal or better weed control than standard treatments at very much lower application rates.

Studies conducted from 19920 to 1995, showed that rimsulfuron alone gave 100% control of wild radish, 68-70% control of corn spurry and 75-90% control of narrowleaf goldenrod. The control level for corn spurry was found to be elevated when rimsulfuron was used in combination with metribuzin.

Field trials conducted in 2005 in Ontario, Canada showed that when rimsulfuron was applied post-emergically to field corn, it provided little visual control of wirestem muhly.
CropUse
CropUses:
maize, potatoes, tomatoes

Maize

15 g ai/ha

Potatoes

10-35 g ai/ha



Premix
Thifensulfuron-methyl+rimsulfuron
Rimsulfuron+metribuzin
Rimsulfuron+Mesotrione+Fluroxypyr-meptyl
Rimsulfuron+Mesotrione
Rimsulfuron+Haloxyfop-P-methyl
Rimsulfuron+chlorimuron-ethyl+mesotrione
Nicosulfuron+rimsulfuron
Nicosulfuron+atrazine+rimsulfuron
Metribuzin+Clethodim+Rimsulfuron
Dry flowable. Premix Parters: acifluorfen bentazone;

Type

AI concn

Water-dispersible granule (WG)

25% (w/w)

Physical Properties
Molecular weight:431.4g/mol; Physical form:Colourless crystals. Density:0.784 (25℃); Composition:Tech. is 99%. Melting point:176-178℃; Vapour pressure:1.5 ×SYM> 10-3 mPa (25℃); Partition coefficient(n-octanol and water):logP = 0.288 (pH 5), -1.47 ( pH 7) (25℃); pKa:4.0; Solubility:In water (25℃) <10 mg/l (unbuffered); 7.3 g/l (buffered, pH 7).; Stability:On hydrolysis (25℃),DT50 4.6 d (pH 5), 7.2 d (pH 7), 0.3 d ( pH 9).;
Toxicology
Oral:Acute oral LD50 for rats >5000 mg/kg. Percutaneous:Acute percutaneous LD50 for rabbits >2000 mg/kg. Non-irritating to skin; moderately irritating to eyes (rabbits). Non-sensitising to skin (guinea pigs). Inhalation:LC50 (4 h) for rats >5.4 mg/l air. ADI:(EPA) 0.125 mg/kg.
Environmental Profile
Ecotoxicology: 
Bees:LD50 (contact) >100 mg/bee; (dietary) >1000 ppm.Fish: (96 h) LC50 >1000 mg/l (bluegill, rainbow trout). Birds:Acute oral LD50 for bobwhite quail >2250, mallard ducks >2000 mg/kg. Dietary LC50 for bobwhite quail and mallard ducks >5620 ppm.Daphnia: LC50 (48 h) >360 mg/l.Fish:LC50 (96 h) for bluegill sunfish and rainbow trout >390, carp >900, sheepshead minnow 110 mg/l.Worms:LC50 (14 d) for earthworms (Eisenia foetida) >1000 mg/kg. 

Environmental fate: 
Animals:Rapidly metabolised and excreted in the urine and faeces.Soil:Degraded rapidly in soil, predominantly via chemical pathways (microbial degradation plays a minor role). Major metabolite is [1-(3-ethylsulfonyl)-2-pyridinyl]-4,6-dimethoxy-2-pyrimidineamine. Rates of degradation are influenced by pH, anPlant:Half-life in maize 6 h, blackgrass 46 h, Johnsongrass 25 d and Sorghum bicolor 52 d. See also Biochemistry.
Transport Information
Signal Word:CAUTION; Hazard Class:III(Slightly hazardous)

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