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Fluroxypyr

PESTANAL®, analytical standard

Synonym(e):

2-[(4-Amino-3,5-dichlor-6-fluor-2-pyridinyl)-oxy]-essigsäure, 4-Amino-3,5-dichlor-6-fluor-2-pyridyloxyessigsäure

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About This Item

Empirische Formel (Hill-System):
C7H5Cl2FN2O3
CAS-Nummer:
69377-81-7
Molekulargewicht:
255.03
Beilstein:
7136185
MDL-Nummer:
MFCD01311822
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756939
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

Nc1c(Cl)c(F)nc(OCC(O)=O)c1Cl

InChI

1S/C7H5Cl2FN2O3/c8-3-5(11)4(9)7(12-6(3)10)15-1-2(13)14/h1H2,(H2,11,12)(H,13,14)

InChIKey

MEFQWPUMEMWTJP-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung


  • Impact of herbicide runoff: Research compares runoff losses and toxicity between residual and knockdown herbicides, including Fluroxypyr, when applied to sugarcane fields, demonstrating significant differences relative to traditional treatments such as Diuron. This study underscores the importance of selecting appropriate herbicide treatments for effective weed management while minimizing environmental impact (Silburn et al., 2023).

  • Herbicide resistance and management: A study focused on Florasulam-resistant flixweed in North China highlights the potential role of alternative herbicides, including Fluroxypyr, for managing resistant weed populations. The research provides insights into herbicide selectivity and efficacy, aiding in the development of more effective weed management strategies (Wang et al., 2021).

  • Herbicide pollution assessment: Utilizing a multi-dimensional approach, this study assesses herbicide pollution in catchment areas, discussing the implications of Fluroxypyr among other herbicides. It focuses on the ecological consequences of herbicide use and the necessity for accurate pollution assessment techniques to ensure environmental safety (Khan et al., 2020).

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

H-Sätze

H412

P-Sätze

P273 - P501

Gefahreneinstufungen

Aquatic Chronic 3

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Jasmin Shah et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(1), 145-146 (2006-01-25)
The starane herbicide was spectrophotometrically determined by the diazotization method in a flow injection assembly. Since starane is a substituted pyridyl compound the NH2 group at the p-position was exploited for diazotization. Starane was diazotized with nitrite and the diazotized
H Cederlund et al.
Journal of environmental quality, 41(6), 1884-1892 (2012-11-07)
Fluroxypyr is an auxin-type herbicide used for postemergent control of broad-leaved weeds in agriculture and in nonagricultural environments such as railways. The overall aim of this study was to assess the potential environmental impact from fluroxypyr application to railway tracks
M Halimah et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 39(5-6), 765-777 (2004-12-29)
Four methods were developed for the analysis of fluroxypyr in soil samples from oil palm plantations. The first method involved the extraction of the herbicide with 0.05 M NaOH in methanol followed by purification using acid base partition. The concentrated
M Kah et al.
Chemosphere, 68(7), 1335-1343 (2007-02-27)
Adsorption of six pesticides (2,4-D, dicamba, fluroxypyr, fluazifop-P, metsulfuron-methyl and flupyrsulfuron-methyl) in nine contrasting soils was measured using two techniques: (i) a classical batch method and (ii) a centrifugation method that allowed the measurement of adsorption at a realistic soil
Michael Hansen et al.
Journal of experimental botany, 60(1), 153-167 (2008-11-19)
The aim of the study was to describe the molecular and biochemical interactions associated with amino acid biosynthesis and storage protein accumulation in the developing grains of field-grown barley. Our strategy was to analyse the transcription of genes associated with
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