Quizalofop-ethyl

Quizalofop-ethyl
Quizalofop-ethyl
Quizalofop-ethyl

Quizalofop-ethyl

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100 Kilogram

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  • Min.Order :100 Kilogram
  • Purity: 99%
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Keywords

Quizalofop-ethyl 76578-14-8 C19H17ClN2O4

Quick Details

  • Appearance:powder
  • Application:76578-14-8
  • PackAge:Depended
  • ProductionCapacity:300|Kilogram|Month
  • Storage:Store in dry, dark and ventilated place
  • Transportation:by air or by sea

Superiority:

Quizalofop-ethyl Basic information
Product Name: Quizalofop-ethyl
Synonyms: TARGA;QUIZALOFOP-ETHYL;QUIZALOOFOP;PILOT;ETHYL-2-[4-[(6-CHLORO-2-QUINOXALINYL)-OXYL]-PHENOXY]PROPIONATE;ETHYL 2-[4-(6-CHLORO-2-QUINOXALINYLOXY)PHENOXY]PROPIONATE;ASSURE;ASSURE WEED KILLER(R)
CAS: 76578-14-8
MF: C19H17ClN2O4
MW: 372.8
EINECS:  
Product Categories:  
Mol File: 76578-14-8.mol
Quizalofop-ethyl Structure
 
Quizalofop-ethyl Chemical Properties
Fp  100 °C
storage temp.  0-6°C
Merck  13,8178
CAS DataBase Reference 76578-14-8(CAS DataBase Reference)
NIST Chemistry Reference Assure(76578-14-8)
EPA Substance Registry System Propanoic acid, 2-[4-[(6-chloro-2-quinoxalinyl) oxy]phenoxy]-, ethyl ester(76578-14-8)
 
Safety Information
Hazard Codes  Xn
Risk Statements  21/22
Safety Statements  22-24/25
RIDADR  UN3077 9/PG 3
RTECS  UA2458255
Hazardous Substances Data 76578-14-8(Hazardous Substances Data)
MSDS Information
 
 
Quizalofop-ethyl Usage And Synthesis
General Description White crystals. Insoluble in water. Used as an herbicide.
Air & Water Reactions Insoluble in water.
Reactivity Profile A halogenated ester and amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

 

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