Prosulfuron
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
- Product Categories:
-
- Herbicides
- N-PAlphabetic
- PON - PTPesticides&Metabolites
- P
- Pesticides&Metabolites
- Urea structure
- Alpha sort
- Mol File:
- 94125-34-5.mol
Prosulfuron Chemical Properties
- Melting point:
- 155° (dec)
- Density
- 1.462±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 4.30±0.10(Predicted)
- BRN
- 7800481
- LogP
- 3.020 (est)
- CAS DataBase Reference
- 94125-34-5(CAS DataBase Reference)
- EPA Substance Registry System
- Prosulfuron (94125-34-5)
Safety Information
- 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.
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Prosulfuron(94125-34-5)Related Product Information
- Methylparaben
- Phenylmethylsulfonyl fluoride
- Methanol
- Methyl acrylate
- PHENYL VALERATE
- FLORASULAM
- TOLBUTAMIDE
- CHLORPROPAMIDE
- Triflusulfuron-methyl
- Basic Violet 1
- Acetonitrile
- Chlorosulfonyl isocyanate
- Trifloxysulfuron
- Trifluoromethanesulfonyl chloride
- 2-Methoxyethanol
- SULFURYL FLUORIDE
- Rimsulfuron
- Methyl