Identification | Back Directory | [Name]
FLUAZIFOP-BUTYL | [CAS]
69806-50-4 | [Synonyms]
pp009 ih773b sl-236 tf1169 PP 009 ts-7236 TF 1169 ONECIDE halokon IH 773B FUSILADE onecideec Fuazifop-butyl HACHE UNO SUPER FLUAZIFOP-BUTYL Fluazipop-butyl. FLUAZIFOP-BUTYL D9 Fluazifop(freeacid) Paraforaldehyde-d(2) Fluazifop, butyl ester FLUAZIFOP-BUTYL STANDARD Fluazifop-butyl solution PARAFORMALDEHYDE (D2, 99%) fluazifop-butyl (bsi,iso,ansi) FLUAZIFOP-BUTYL PESTANAL, 250 MG Fluazifop-butyl 250mg [69806-50-4] Fluazifop-butylSolution,100mg/L,1ml Fluazifop-butyl Solution in Methanol, 1000μg/mL BUTYL(RS)-2-(4-((5-(TRIFLUOROMETHYL)-2-PYRIDINYL)OXY)PHENO. BUTYL(R)-2-(4-((5-(TRIFLUOROMETHYL)-2-PYRIDINYL)OXY)PHENOX. butyl2-(4-(5-trifluoromethyl-2-pyridinyloxy)phenoxy)propanoate BUTYL 2-[4-(5-TRIFLUOROMETHYL-2-PYRIDYLOXY)-PHENOXY]PROPIONATE Butyl-2-[4-(5-trifluoromethyl-2-pyridinyloxy)phenoxy]propionate Butyl 2-(4-(5-trifluoromethyl-2-pyridinyloxy)phenoxy)propanoate butyl 2-[4-[5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]propanoate Butyl (RS)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionate 2-(p-((5-(trifluoromethyl)-2-pyridyl)oxy)phenoxy)-propionicacibutylest 2-(4-((5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)-propanoicacibutylest 2-[4-(5-Trifluoromethylpyridin-2-yloxy)phenoxy]propionic acid butyl ester 2-[4-[(5-Trifluoromethyl-2-pyridinyl)oxy]phenoxy]propionic acid butyl ester 2-[4-[[5-(trifluoromethyl)-2-pyridyl]oxy]phenoxy]propionic acid butyl ester 2-[4-[[5-(Trifluoromethyl)-2-pyridinyl]oxy]phenoxy]-propanoicacidbutylester Propanoicacid,2[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]-,butylester 2-[4-[[5-(Trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid butyl ester Propionic acid, 2-(p-((5-(trifluoromethyl)-2-pyridyl)oxy)phenoxy)-, butyl ester Propanoic acid, 2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]-, butyl ester fluazifop-butyl (ISO) butyl (RS)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionate | [EINECS(EC#)]
274-125-6 | [Molecular Formula]
C19H20F3NO4 | [MDL Number]
MFCD00870330 | [MOL File]
69806-50-4.mol | [Molecular Weight]
383.36 |
Chemical Properties | Back Directory | [Appearance]
Pale straw-colored, odorless liquid. | [Melting point ]
13°C | [Boiling point ]
bp0.05 167° | [density ]
1.2100 | [Fp ]
2 °C | [storage temp. ]
0-6°C | [form ]
neat | [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) |
Hazard Information | Back Directory | [Chemical Properties]
Pale straw-colored, odorless liquid. | [Uses]
Food additive; herbicide; agricultural chemical. | [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. | [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. | [First aid]
If this chemical gets into the eyes, remove any
contact lenses at once and irrigate immediately for at least
15 minutes, occasionally lifting upper and lower lids. Seek
medical attention immediately. If this chemical contacts the
skin, remove contaminated clothing and wash immediately
with soap and water. Seek medical attention immediately.
If this chemical has been inhaled, remove from exposure,
begin rescue breathing (using universal precautions) if
breathing has stopped, and CPR if heart action has stopped.
Transfer promptly to a medical facility. When this chemical
has been swallowed, get medical attention. Do not induce
vomiting when formulations containing petroleum solvents
are ingested. Otherwise, give large quantities of water and
induce vomiting. Do not make an unconscious person
vomit. | [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. | [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. | [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® | [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. |
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