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FLUFENPYR-ETHYL

FLUFENPYR-ETHYL Suppliers list
Company Name: Alta Scientific Co., Ltd.  
Tel: 022-6537-8550 15522853686
Email: sales@altasci.com.cn
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Shandong Xiya Chemical Co., Ltd.  
Tel: 4009903999 13395398332
Email: sales@xiyashiji.com
Company Name: Shandong Ono Chemical Co., Ltd.  
Tel: 0539-6362799 20)
Email:
Company Name: Dideu Industries Group Limited  
Tel: +8617392712697
Email: 1022@dideu.com

FLUFENPYR-ETHYL manufacturers

  • FLUFENPYR-ETHYL
  • FLUFENPYR-ETHYL  pictures
  • $1.10
  • 2026-08-20
  • CAS:188489-07-8
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons Min
FLUFENPYR-ETHYL Basic information
Product Name:FLUFENPYR-ETHYL
Synonyms:FLUFENPYR-ETHYL;flufenpyr-ethyl (bsi, pa iso);s-3153;FLUFENPYL-ETHYL STANDARD;Flufenpyr-ethyl@100 μg/mL in Acetonitrile;Flufenpyr-ethyl Standard;Flufenpyr-ethyl@1000 μg/mL in Acetonitrile;Acetic acid, 2-[2-chloro-4-fluoro-5-[5-methyl-6-oxo-4-(trifluoromethyl)-1(6H)-pyridazinyl]phenoxy]-, ethyl ester
CAS:188489-07-8
MF:C16H13ClF4N2O4
MW:408.73
EINECS:
Product Categories:
Mol File:188489-07-8.mol
FLUFENPYR-ETHYL Structure
FLUFENPYR-ETHYL Chemical Properties
Boiling point 440.1±55.0 °C(Predicted)
density 1.45±0.1 g/cm3(Predicted)
pka-3.03±0.60(Predicted)
EPA Substance Registry SystemFlufenpyr-ethyl (188489-07-8)
Safety Information
MSDS Information
FLUFENPYR-ETHYL Usage And Synthesis
DefinitionChEBI: An ethyl ester resulting from the formal condesnation of the carboxy group of flufenpyr with ethanol. It is used as a contact herbicide for the control of broad-leaved weeds. It acts as a protoporphyrinogen oxidase inhibitor, causing protoporphyrins to acc mulate, damaging the membrane structure and cellular function. No longer approved for use in the European Union.
Production MethodsFlufenpyr-ethyl is commercially produced through a multi-step synthesis involving the condensation of 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-4-methyl-5-(trifluoromethyl)-3(2H)-pyridazinone with ethyl bromoacetate. This reaction forms the ethyl ester of a phenoxyacetic acid derivative, incorporating a pyridazinone ring with multiple halogen substitutions for enhanced herbicidal activity. The synthesis is typically carried out under reflux in polar aprotic solvents, followed by purification steps such as crystallisation or chromatography.
Mechanism of actionProtoporphyrinogen oxidase inhibitor
Pesticide TypeHerbicide
FLUFENPYR-ETHYL Preparation Products And Raw materials
Raw materials2-(4-Chloro-2-fluoro-5-hydroxyphenyl)-4-methyl-5-(trifluoromethyl)-3(2H)-pyridazinone-->Ethyl bromoacetate
Tag:FLUFENPYR-ETHYL(188489-07-8) Related Product Information
Orthosulfamuron Rimantadine hydrochloride Flumethasone Chlorothalonil Flufenpyr-ethyl 4'-Chloro-2'-fluoroacetanilide 3-Amino-2,6-dimethylpyridine CHEMBRDG-BB 9031620 SALOR-INT L497096-1EA 3-Amino-4-fluorophenol 3-ETHOXY-PHENYL-HYDRAZINE (2-CHLORO-4-FLUOROPHENOXY)ACETIC ACID 3-Methoxyphenylhydrazine hydrochloride (4-FLUOROPHENOXY) ACETIC ACID ETHYL ESTER 4-Fluorophenoxyacetic acid