ChemicalBook > Product Catalog >Chemical pesticides >Herbicide >Prosulfuron

Prosulfuron

Prosulfuron Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Syntechem Co.,Ltd  
Tel:
Email: info@syntechem.com
Company Name: Sichuan Kulinan Technology Co., Ltd  
Tel: 400-1166-196 18981987031
Email: cdhxsj@163.com
Company Name: UHN Shanghai Research & Development Co., Ltd.  
Tel: 021-58958002 18930822973
Email: sales@uhnshanghai.com
Company Name: Nanjing Sunlida Biological Technology Co., Ltd.  
Tel: 025-57798810 18652991625
Email: sales@sunlidabio.com

Prosulfuron manufacturers

  • Prosulfuron
  • Prosulfuron pictures
  • $1.00
  • 2020-01-13
  • CAS:94125-34-5
  • Min. Order: 1g
  • Purity: 99.0%
  • Supply Ability: 100kg
Prosulfuron Basic information
Product Name:Prosulfuron
Synonyms: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;CGA152005
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 Structure
Prosulfuron Chemical Properties
Melting point 155° (dec)
density 1.462±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka4.30±0.10(Predicted)
BRN 7800481
Henry's Law Constant3.3×103 mol/(m3Pa) at 25℃, Maniere et al. (2011)
LogP3.020 (est)
CAS DataBase Reference94125-34-5(CAS DataBase Reference)
EPA Substance Registry SystemProsulfuron (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 Data94125-34-5(Hazardous Substances Data)
ToxicityLD50 orally in rats: 986 mg/kg; dermally in rabbits: >2000 mg/kg; LC50 (4 hr) by inhalation in rats: >5000 mg/m3 (Schulte)
MSDS Information
Prosulfuron Usage And Synthesis
DescriptionProsulfuron is a broad-spectrum herbicide. It is highly soluble in water and many organic solvents, is volatile, mobile and has a high potential for leaching to groundwater. It is generally moderately persistent in soil systems but can be very persistent in aquatic systems. It is moderately toxic to mammals but is not expected to bioaccumulate. It is moderately toxic to birds, honeybees, earthworms and fish but less so to aquatic invertebrates. It is highly toxic to algae and aquatic plants.
Chemical PropertiesFlusulfuron pure product is colorless and odorless crystal, purity ≥95%. Melting point 155°C (decomposition). Vapor pressure≤3.5×10-3mPa(25℃). Distribution coefficient Kow lg(25℃);1.5(pH 5.0),-0.21(pH 6.9),-0.76(pH 9.0).Henry value<3×10-4Pa -m3/ mol.Solubility in water(25℃ , mg/L):distilled water29(pH4.5),buffer solution:87(pH 5.0),4000(pH 6.8),43000(pH 6.8). 6.8), 43000 (pH 7.7). Solubility in organic solvents (25°C,g/L):ethanol 8.4, acetone 160, toluene 6.1, n-hexane 0.0064, n-octanol 1.4, ethyl acetate 56, dichloromethane 180.Stability:Rapidly hydrolyzable, DT505~10d(pH 5),>ly(pH 7,9)(both at 20°C). Stable to light, pKa3.76.
UsesHerbicide.
DefinitionChEBI: Prosulfuron is a member of triazines.
Agricultural UsesHerbicide: 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 nameCGA®-152005; EXCEED®; PEAK®; SPIRIT®
Mechanism of actionAbsorbed by leaves and roots. Inhibits plant amino acid synthesis - acetohydroxyacid synthase AHAS
SynthesisSynthetic route for Prosulfuron intermediate by Ciba-Geigy/Novartis.[1]
Prosulfuron synthesis
Metabolic pathwayAs 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.
References[1] Jagtap, S. Heck Reaction—State of the Art. Catalysts 2017, 7, 267. DOI:10.3390/catal7090267
Pesticide TypeHerbicide
Prosulfuron Preparation Products And Raw materials
Tag:Prosulfuron(94125-34-5) Related Product Information
Methylparaben Phenylmethylsulfonyl fluoride Methanol Methyl acrylate FLORASULAM Triflusulfuron-methyl Basic Violet 1 Chlorosulfonyl isocyanate Trifloxysulfuron Trifluoromethanesulfonyl chloride 2-Methoxyethanol Rimsulfuron SULFURYL FLUORIDE Acetonitrile Phenyl valerate Tolbutamide Chlorpropamide Methyl