| Identification | More | [Name]
Prosulfuron | [CAS]
94125-34-5 | [Synonyms]
1-(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenylsulfonyl]urea
EXCEED
PEAK
PROSULFURON
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
CGA152005
N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]-2-(3,3,3-trifluoropropyl)benzenesulfonamide
prosulfuron 1-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenylsulfonyl]urea | [Molecular Formula]
C15H16F3N5O4S | [MDL Number]
MFCD01863141 | [Molecular Weight]
419.38 | [MOL File]
94125-34-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
R22:Harmful if swallowed.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [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) |
| Hazard Information | Back Directory | [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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