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| | Prosulfuron Basic information |
| Product Name: | Prosulfuron | | Synonyms: | PEAK;PROSULFURON;EXCEED;1-(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenylsulfonyl]urea;N-((3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino)carbonyl)-2-(3,3,3-trifluoropropyl)benzone sulfnamide;PROSULFURON PESTANAL, 100 MG;prosulfuron (bsi, pa e-iso);PROSULPHURON | | CAS: | 94125-34-5 | | MF: | C15H16F3N5O4S | | MW: | 419.38 | | EINECS: | | | Product Categories: | Herbicides;N-PAlphabetic;P;Pesticides&Metabolites;Urea structure;PON - PTPesticides&Metabolites;Alpha sort | | Mol File: | 94125-34-5.mol |  |
| | Prosulfuron Chemical Properties |
| Hazard Codes | Xn,N | | Risk Statements | 22-50/53 | | Safety Statements | 60-61 | | RIDADR | UN3077 9/PG 3 | | WGK Germany | 3 | | Hazardous Substances Data | 94125-34-5(Hazardous Substances Data) | | Toxicity | LD50 orally in rats: 986 mg/kg; dermally in rabbits: >2000 mg/kg; LC50 (4 hr) by inhalation in rats: >5000 mg/m3 (Schulte) |
| | Prosulfuron Usage And Synthesis |
| Uses | Herbicide. | | Definition | ChEBI: Prosulfuron is a member of triazines. | | Agricultural Uses | Herbicide: Used as a post-emergence herbicide on corn and cereals such as barley, millet, oats, rye, sorghum and wheat. Used on sugar cane in some countries. Currently registered in some EU countries. Registered for use in the U.S. | | Trade name | CGA®-152005; EXCEED®; PEAK®; SPIRIT® | | Metabolic pathway | As shown below, the degradation profiles of
prosulfuron by hydrolysis, mammal, soil
microorganism, plant, plant microsome, and soil are well investigated. In addition to the degradation
products derived by the common cleavage reaction of
the sulfonylurea linkage, the predominant
hydroxylation reaction occurs on the phenyl ring and
the trifluoropropyl side chain by mammal and soil
microorganisms, resulting in the formation of the
hydroxylated metabolites which mostly retain the
sulfonylurea moiety in the structures. |
| | Prosulfuron Preparation Products And Raw materials |
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