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Fluazifop-butyl

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Fluazifop-butyl Basic information

Product Name:
Fluazifop-butyl
Synonyms:
  • Fluazifop-butyl solution
  • 2-[4-(5-Trifluoromethylpyridin-2-yloxy)phenoxy]propionic acid butyl ester
  • 2-[4-[(5-Trifluoromethyl-2-pyridinyl)oxy]phenoxy]propionic acid butyl ester
  • fluazifop-butyl (ISO) butyl (RS)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionate
  • 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propionic acid butyl ester
  • butyl 2-[4-[5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]propanoate
  • Fluazifop-butyl 250mg [69806-50-4]
  • FUSILADE
CAS:
69806-50-4
MF:
C19H20F3NO4
MW:
383.36
EINECS:
274-125-6
Product Categories:
  • Alpha sort
  • E-GAlphabetic
  • F
  • FA - FLEnvironmental Standards
  • Herbicides
  • MetabolitesPesticides&Metabolites
  • Pesticides&Metabolites
  • Phenoxy structure
Mol File:
69806-50-4.mol
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Fluazifop-butyl Chemical Properties

Melting point:
13°C
Boiling point:
bp0.05 167°
Density 
1.2100
Flash point:
2 °C
storage temp. 
0-6°C
pka
0.78±0.22(Predicted)
Water Solubility 
536.6ug/L(temperature not stated)
Merck 
13,4142
EPA Substance Registry System
Fluazifop-butyl (69806-50-4)
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Safety Information

Hazard Codes 
T,N,Xn,F
Risk Statements 
61-50/53-36-20/21/22-11
Safety Statements 
53-45-60-61-36-26-16
RIDADR 
UN3082 9/PG 3
WGK Germany 
3
RTECS 
UA3000000
HS Code 
29333990
Hazardous Substances Data
69806-50-4(Hazardous Substances Data)
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Fluazifop-butyl Usage And Synthesis

Chemical Properties

Pale straw-colored, odorless liquid.

Chemical Properties

Pale yellow liquid. Odorless.

Uses

Food additive; herbicide; agricultural chemical.

Uses

Fluazifop-butyl-d9 is the labeled version of Fluazifop-butyl (F407433), which is often found in herbicidal and fungicidal mixture compositions.

Definition

ChEBI: Butyl 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate is a carboxylic ester resulting from the formal condensation of the carboxy group 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid with the hydroxy group of butan-1-ol. It is a carboxylic ester, an organofluorine compound, a member of pyridines and an aromatic ether. It is functionally related to a 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid and a butan-1-ol.

General Description

A pale straw colored liquid. Selective herbicide.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

FLUAZIFOP-BUTYL is a trimethyl phenoxy pyridine ester. May react with acids to liberate heat. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. May generate heat with caustic solutions. Genreates flammable hydrogen with alkali metals and hydrides.

Hazard

Moderately toxic by ingestion.

Agricultural Uses

Herbicide: Fluazifop-butyl is a selective post-emergence herbicide. Its principal uses in California is on rights-of-way, landscapes, almonds, cotton, and outdoor container nurseries. Not approved for use in EU countries. Not registered for use in the U.S. Used in southeast Asia. There are 18 global suppliers.

Trade name

FUSILADE®[C]; FUSILADE® MAX (P-butyl); FUSION®; GRASS-B-GONE®; Greencrop; HACHE UNO SUPER®; HORIZON®; ICI-A0009®; ONESIDE®; ONESIDE EC®; ORNAMEC®; PP 009®; SL-236®; TF 1169®; TS-7236®; TORNADO®

Potential Exposure

Fluazifop-butyl is a selective post emergence aryloxyphenoxypropionate/organofluorine herbi cide. Its principal uses In California is on rights-of-way, landscapes, almonds, cotton, and outdoor container nurseries.

Metabolic pathway

Fluazifop butyl as a thin film on glass is photorearranged by UV irradiation to the isomer butyl-(RS)-2-[4-hydroxy-3-(5-trifluoromethyl-2- pyridyl)phenoxy]propionate. Plants of both resistant and susceptible populations of Digitaria sanguinalis rapidly hydrolyze 14C-fluazifop butyl to corresponding acid in leaves, but fluazifop acid is metabolized to other compounds at a more rapid rate in the resistant plants. An enhanced metabolism of toxophore, fluazifop acid is a likely mechanism of resistance in this population. The plants of putative resistant and susceptible population of Digitaria sanguinalis (L.) Scop had survived the application of 212 g/ha fluazifop-P-butyl in the year of collection.

Waste Disposal

In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Containers must be dis posed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Fluazifop-butyl Preparation Products And Raw materials

Raw materials

Fluazifop-butyl Supplier

Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Email
sales@sunlidabio.com
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Raw material medicin reagent co.,Ltd
Tel
025-57798860
Email
sales@njromanme.com
Chongqing Chemieliva Pharmaceutical Co., Ltd.
Tel
023-67770219
Email
jessica.hu@chemieliva.com
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com