Fluroxypyr CAS 69377-81-7

Introduction:Basic information about Fluroxypyr CAS 69377-81-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Fluroxypyr Basic information

Product Name:Fluroxypyr
Synonyms:((4-amino-3,5-dichloro-6-fluoro-2-pyridinyl)oxy)-aceticaci;4-amino-3,5-dichloro-6-fluoro-2-pyridyloxyaceticacid;ff4014;[(4-Amino-3,5-dichloro-6-fluoropyridin-2-yl)oxy]acetic acid;2-[(4-AMino-3,5-dichloro-6-fluoro-2-pyridinyl)oxy]acetic Acid;Fluroxypyr Solution, 1000ppm;2-((4-Amino-3,5-dichloro-6-fluoropyridin-2-yl)oxy)acetic acid;Aceticacid, 2-[(4-amino-3,5-dichloro-6-fluoro-2-pyridinyl)oxy]-
CAS:69377-81-7
MF:C7H5Cl2FN2O3
MW:255.03
EINECS:200-001-8
Product Categories:Alpha sort;E-GAlphabetic;F;FA - FLPesticides&Metabolites;Herbicides;Pesticides&Metabolites;Pyridine
Mol File:69377-81-7.mol

Fluroxypyr Chemical Properties

Melting point 57.5°C
Boiling point 399.4±37.0 °C(Predicted)
density 1.3
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
pka2.22±0.10(Predicted)
color White to Off-White
Merck 13,4229
BRN 7136185
Major Applicationagriculture
environmental
InChI1S/C7H5Cl2FN2O3/c8-3-5(11)4(9)7(12-6(3)10)15-1-2(13)14/h1H2,(H2,11,12)(H,13,14)
InChIKeyMEFQWPUMEMWTJP-UHFFFAOYSA-N
SMILESNc1c(Cl)c(F)nc(OCC(O)=O)c1Cl
LogP3.160 (est)
CAS DataBase Reference69377-81-7(CAS DataBase Reference)
NIST Chemistry ReferenceFluroxypyr(69377-81-7)
EPA Substance Registry SystemFluroxypyr (69377-81-7)

Safety Information

Risk Statements 52/53
Safety Statements 61
RIDADR UN3077(solid)
WGK Germany 2
RTECS AF2500000
Storage Class11 - Combustible Solids
Hazard ClassificationsAquatic Chronic 3
Hazardous Substances Data69377-81-7(Hazardous Substances Data)
ToxicityLD50 orally in rats: 2405 mg/kg; i.p. in male, female rats: 458, 519 mg/kg; percutaneous in rabbits >5000 mg/kg (Paul)

Fluroxypyr Usage And Synthesis

Chemical PropertiesWhite crystalline solid.
UsesFluroxypyr is a systemic and selective herbicide. Fluroxypyr is used for the control of broad-leaved weeds in small grain cereals, maize, pastures, range land and turf. Fluroxypyr is a synthetic auxin.
DefinitionChEBI: An aminopyridine that is pyridin-4-amine substituted by chloro groups at positions 3 and 5, a fluoro group at position 6 and a carboxymethoxy group at position 2.
Trade namemethyl ester: AGROSTAR; BOFIX FFC®;CABADEX®; CASCADE®; DOWCO® 433 MHE;FOREFRONT®; GALAXY GL184®; PARADIGM®;PASTUREGARD®; STARANE®; TOMAHAWK®;VISTA®; WIDEMATCH®, (fluroxypyr + clopyralid);XRM-5084®
Potential ExposureThose who manufacture, distribute oruse this pyridinecarboxylic acid/pyridine herbicide.
Environmental FateThe DT50 in soil is relatively short,ranging from 5 to 9 days in experiments conducted inthe laboratory. This rapid degradation is due to microbes.Because of its rapid soil degradation, little fluroxypyr isavailable for other dissipation processes, e.g., leaching.
MetabolismFluroxypyr is stable under acidic conditionsand moderately stable in alkaline conditions; e.g., theDT50 in water at pH 9 is 185 days. Degradation occurs attemperatures above its melting point. Fluroxypyr is stablein light.
Plant. The metabolism of fluroxypyr has not been fullydescribed. Conjugates of fluroxypyr have been observed intolerant plants.
Soil. Fluroxypyr is rapidly metabolized by soilmicrobes via the removal of the carboxyl group oracetic acid group, yielding 4-amino-3,5-dichloro-6-fluoro-2-methoxypyridine, and 4-amino-3,5-dichloro-6-fluoro-2-pyridinol, respectively.
ShippingUN3077 Environmentally hazardous substances,solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous haz ardous material, Technical Name Required.
Toxicity evaluationMammalian Toxicity. Fluroxypyr appears to be rapidlyexcreted, unmodified, in the urine of animals. The acuteoral LD50 for rat is 2405 mg/kg.
Weed Resistance/Modified Crop Tolerance. Fuerst et al.(48) reported fluroxypyr resistance in yellow starthistle(Centaurea solstitialis). No crops with modified tolerancetoward fluroxypyr are currently in production.
IncompatibilitiesMay not be compatible with nitrates.Moisture may cause hydrolysis or other forms of decompo sition; forming a strong acid. Temperatures above 250℃ can cause decomposition. Methyl ester: Esters react withacids to liberate heat along with alcohols and acids. Strongoxidizing acids may cause a vigorous reaction that is suffi ciently exothermic to ignite the reaction products. Heat isalso generated by the interaction of esters with caustic solu tions. Flammable hydrogen is generated by mixing esterswith alkali metals and hydrides.
Waste DisposalContainers must be disposedof properly by following package label directions or bycontacting your local or federal environmental controlagency, or by contacting your regional EPA office.Dissolve or mix the material with a combustible solventand burn in a chemical incinerator equipped with an after burner and scrubber. In accordance with 40CFR165, followrecommendations for the disposal of pesticides and pesti cide containers.

Fluroxypyr Preparation Products And Raw materials

Raw materialsFlupirtine-->Ethyl glycolate-->3,5-Dichloro-2,4,6-trifluoropyridine-->4-Amino-3,5-dichloro-2,6-difluoropyridine-->Pentachloropyridine
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