69806-50-4 Usage
Uses
Used in Agriculture:
FLUAZIFOP-BUTYL is used as a herbicide for controlling broadleaf and grassy weeds in various crops, such as cereals, corn, and soybeans. It targets the growth and development of weeds, reducing competition for resources and improving crop yield.
Used in Food Industry:
FLUAZIFOP-BUTYL is used as a food additive to ensure the quality and safety of food products. It helps in maintaining the freshness and preventing spoilage of food items by controlling the growth of unwanted microorganisms.
Used in Pest Control:
FLUAZIFOP-BUTYL is used as a fungicide to protect plants from fungal infections and diseases. It is effective in controlling various fungal pathogens, thereby reducing crop losses and ensuring a healthy growth of plants.
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.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 69806-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69806-50:
(7*6)+(6*9)+(5*8)+(4*0)+(3*6)+(2*5)+(1*0)=164
164 % 10 = 4
So 69806-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H20F3NO4/c1-3-4-11-25-18(24)13(2)26-15-6-8-16(9-7-15)27-17-10-5-14(12-23-17)19(20,21)22/h5-10,12-13H,3-4,11H2,1-2H3
69806-50-4Relevant academic research and scientific papers
NOXIOUS ARTHROPOD CONTROL AGENT CONTAINING AMIDE COMPOUND
-
, (2017/08/26)
An object of the present invention is to provide a compound having the controlling activity on a noxious arthropod, and a noxious arthropod controlling agent containing an amide compound of formula (I): wherein X represents a nitrogen atom or a CH group, p represents 0 or 1, A represents a tetrahydrofuranyl group or the like, R1, R2, R3, R4, R5, R6 and R7 represent a hydrogen atom or the like, n represents 1 or 2, Y represents an oxygen atom or the like, m represents any integer of 0 to 7, and Q represents a C1-8 chain hydrocarbon group optionally having a phenyl group or the like, has the excellent noxious arthropod controlling effect.
Sulfamoylphenylureas
-
, (2008/06/13)
The N-acylsulfamoylphenylureas of formula I below are suitable as counter-agents (antidotes or safeners) for protecting cultivated plants from the phytotoxic action of herbicides. Suitable crops are preferably cereals, soybeans, sorghum, maize and rice, and suitable herbicides are sulfonylureas, chloroacetanilides and aryloxyphenoxypropionic acid derivatives. The N-acylsulfamoylphenylureas have the formula I STR1 wherein A is a radical selected from the group STR2 R1 is C1 -C4 -alkoxy or each of R1 and R2, independently of the other, is hydrogen, C1 -C8 alkyl, C3 -C8 cycloalkyl, C3 -C6 alkenyl, C3 -C6 alkynyl, STR3 or C1 -C4 alkyl substituted by C1 -C4 alkoxy or by STR4 or R1 and R2 together form a C4 -C6 alkylene bridge, or a C4 -C6 alkylene bridge interrupted by oxygen, sulfur, SO, SO2, NH or by --N(C1 -C4 alkyl)-, R3 is hydrogen or C1 -C4 alkyl, Ra to Rh, Rx and Ry are as defined in the disclosure.
Convenient Synthesis of Phenyl Pyridylethers Utilizing Fluoride Ion
Hwang, Ki-Jun,Park, Seung Ki
, p. 949 - 954 (2007/10/02)
Aryl pyridyl ethers were prepared from phenols and active halopyridines under essentially neutral condition via fluoride ion assisted reaction.
Herbicidal sulfonamides
-
, (2008/06/13)
Compounds of the formula: wherein, R1 is H or CH3; and, R2 is H, F, Cl or CH3;, exhibit herbicidal activity, especially selective activity on rape. The compounds may be made e.g. by reacting the appropriate arylsulfonyl isocyanate with the appropriate aminotriazine.
A process for preparing 2-pyridinyloxyphenoxy-lower-alkanoates
-
, (2008/06/13)
This invention relates to a process for preparing pyridyloxyphenoxypropanecarboxylic acids and their derivatives, and to intermediates useful in the process.
