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carfentrazone-ethyl

carfentrazone-ethyl Suppliers list
Company Name: Sichuan Kulinan Technology Co., Ltd  
Tel: 400-1166-196 18981987031
Email: cdhxsj@163.com
Company Name: Chengdu Ai Keda Chemical Technology Co., Ltd.  
Tel: 4008-755-333 18080918076
Email: 800078821@qq.com
Company Name: Nanjing Sunlida Biological Technology Co., Ltd.  
Tel: 025-57798810 18652991625
Email: sales@sunlidabio.com
Company Name: Shanghai JONLN Reagent Co., Ltd.  
Tel: 400-0066400 13621662912
Email: 422131432@qq.com
Company Name: Alta Scientific Co., Ltd.  
Tel: 022-6537-8550 15522853686
Email: sales@altasci.com.cn

carfentrazone-ethyl manufacturers

  • Carfentrazone
  • Carfentrazone pictures
  • 2024-04-02
  • CAS:128621-72-7
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100 ton
  • carfentrazone-ethyl
  • 	carfentrazone-ethyl pictures
  • $6.60
  • 2019-12-26
  • CAS:128621-72-7
  • Min. Order: 500g
  • Purity: 98%
  • Supply Ability: 1kg, 50kg, 100kg
carfentrazone-ethyl Basic information
Product Name:carfentrazone-ethyl
Synonyms:carfentrazone (free acid);ethyl-(RS)-2-chloro-3-[2-chloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol)-4-fluorophenyl] propionate;F 116426;F 8426;Affinty;ethyl (RS)-2-chloro-3-(2-chloro-5-(4-difluirimethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)-4-fluorophenyl)propionate;ethyl-2-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)-4-fluorobenzenepropanate;2-Chloro-3-[2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-1,2,4-triazol-1-yl]-4-fluorophenyl]propanoic acid
CAS:128621-72-7
MF:C13H10Cl2F3N3O3
MW:384.14
EINECS:
Product Categories:
Mol File:128621-72-7.mol
carfentrazone-ethyl Structure
carfentrazone-ethyl Chemical Properties
Boiling point 472.8±55.0 °C(Predicted)
density 1.67±0.1 g/cm3(Predicted)
solubility DMSO (Slightly), Methanol (Slightly, Sonicated)
pka2.76±0.14(Predicted)
form Solid
color White to Off-White
Stability:Hygroscopic
EPA Substance Registry SystemBenzenepropanoic acid, .alpha.,2-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl]-4-fluoro- (128621-72-7)
Safety Information
MSDS Information
carfentrazone-ethyl Usage And Synthesis
DescriptionCarfentrazone is a herbicide, normally applied as the ethyl variant, used to control a wide range of broadleaved weeds. It is not expected to be persistent in the environment. Little data is available for the acid regarding its ecotoxicology or impacts on environmental health.
Chemical PropertiesPure product is viscous yellow liquid. m.p.-22.1°C, relative density 1.457 (20°C), vapor pressure 1.6×10-5Pa (25°C), partition coefficient 3.36, solubility in water 12μg/L (20°C), 22μg/L (5°C). The half-life in soil is only a few hours.
UsesCarfentrazone is a triazolone herbicide used in the protection of grain and vegetable crops from weeds.
DefinitionChEBI: 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid is a member of the class of triazoles that is 2,4-dihydro-3H-1,2,4-triazol-3-one which is substituted at positions 2, 4, and 5 by 5-(2-carboxy-2-chloroethyl)-4-chloro-2-fluorophenyl, difluoromethyl, and methyl groups, respectively. It is a member of triazoles, a member of monochlorobenzenes, a member of monofluorobenzenes and a monocarboxylic acid.
Production MethodsCarfentraone is usually prepared as the ethyl ester and its commercial follows the route typical of aryl triazolinone herbicides, constructing the triazolinone heterocycle and then attaching the aryl and ethyl ester moieties in controlled steps. Industrial routes generally begin with preparation of a chlorinated or fluorinated benzoic acid derivative, which is then coupled to a hydrazine based intermediate to form the triazolinone ring system through cyclisation and oxidation. Subsequent esterification with ethanol yields the ethyl ester that defines the commercial active ingredient. The process emphasises tight control of halogenation, moisture exclusion, and purification to maintain the required isomeric and impurity profile for herbicide registration and formulation.
Mechanism of actionContact, absorbed by foliage with limited translocation. Inhibition of protoporphyrinogen oxidase (PPO) - cell membrane disruption
Metabolic pathway14C-Carfentrazone is more readily absorbed by the foliage of soybean than by weeds, with 56, 7, and 10% of the applied radioactivity recovered from the foliage of soybean, ivyleaf morning glory, and velvetleaf, respectively. Soybean metabolizes carfentrazone more rapidly than weeds, with 28% of the parent compound remaining in the treated tissue of soybean and 48 and 67% in ivyleaf morning glory and velvetleaf, respectively. All species accumulate similar amounts of the free acid derivative of carfentrazone which is the only identified metabolite. Since both carfentrazone and the free acid are potent inhibitors of protoporphyrinogen oxidase, the result indicates that the tolerance of soybean to carfentrazone may be attributed to its better ability to metabolize carfentrazone to unidentified metabolites, relative to weeds.
Pesticide TypeHerbicide; Metabolite
carfentrazone-ethyl Preparation Products And Raw materials
Raw materialsPyruvic acid-->Ethyl acrylate-->Diphenylphosphoryl azide-->2-Fluoroaniline-->Chlorofluoromethane-->triazoline-->4-Chloro-2-fluoroaniline-->Carfentrazone-ethyl
Preparation ProductsCarfentrazone-ethyl
Tag:carfentrazone-ethyl(128621-72-7) Related Product Information
Triazophos Triadimenol A 1,2,4-Triazolylsodium Triadimenol MCPA SODIUM DITHIANON Triadimefon 1-(3-Propylphenyl)hydrazine hydrochloride (3-Ethyl-phenyl)-hydrazine hydrochloride Carfentrazone-ethyl (4-Chloro-3-methyl-phenyl)-hydrazine hydrochloride 3-(2-Chloro-4-fluoro-phenyl)-propan-1-ol 4-Chloro-2-fluorophenylhydrazine hydrochloride 2-Chloro-4-fluoro-5-methyl aniline carfentrazone-ethyl