Pale yellow liquid. Odorless.
Pale straw-colored, odorless liquid.
Food additive; herbicide; agricultural chemical.
Fluazifop-butyl-d9 is the labeled version of Fluazifop-butyl (F407433), which is often found in herbicidal and fungicidal mixture compositions.
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.
A pale straw colored liquid. Selective herbicide.
Slightly soluble in water.
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.
Moderately toxic by ingestion.
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.
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®
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.
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.
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.
