69806-50-4 Usage
Chemical Properties
Different sources of media describe the Chemical Properties of 69806-50-4 differently. You can refer to the following data:
1. Pale straw-colored, odorless liquid.
2. Pale yellow liquid. Odorless.
Uses
Different sources of media describe the Uses of 69806-50-4 differently. You can refer to the following data:
1. Food additive; herbicide; agricultural chemical.
2. Fluazifop-butyl-d9 is the labeled version of Fluazifop-butyl (F407433), which is often found in herbicidal and fungicidal mixture compositions.
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.
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 articles and documents
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.
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.
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.
