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Supelco

Quizalofop-ethyl

PESTANAL®, analytical standard

Synonym(s):

Ethyl 2-[4-(6-chloro-2-quinoxalinyloxy)phenoxy]propionate

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About This Item

Empirical Formula (Hill Notation):
C19H17ClN2O4
CAS Number:
Molecular Weight:
372.80
Beilstein:
7145610
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCOC(=O)C(C)Oc1ccc(Oc2cnc3cc(Cl)ccc3n2)cc1

InChI

1S/C19H17ClN2O4/c1-3-24-19(23)12(2)25-14-5-7-15(8-6-14)26-18-11-21-17-10-13(20)4-9-16(17)22-18/h4-12H,3H2,1-2H3

InChI key

OSUHJPCHFDQAIT-UHFFFAOYSA-N

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General description

Quizalofop-ethyl is a phenoxy propionate herbicide, which is used to control both annual and perennial grass weeds in broadleaved crops.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Residual behavior of quizalofop ethyl on onion (Allium cepa L.)
Sahoo.K.S, et al.
Environmental Monitoring and Assessment, 185, 1711-1718 (2013)
Metabolism of [14C] quizalofop-ethyl in soybean and cotton plants
Koeppe.KM, et al.
Journal of Agricultural and Food Chemistry, 38, 1085-1091 (1990)
Zhaoyang Li et al.
Chirality, 24(7), 552-557 (2012-05-09)
The enantioselective degradation of quizalofop-ethyl and its metabolite quizalofop-acid in two soils, a Wuhan acidic soil and a Baoding alkaline soil, was investigated. The dissipation of quizalofop-ethyl consisted of two phases, a rapidly deceasing first phase that lasted 1 day
Yoshikatsu Suzuki et al.
Bioscience, biotechnology, and biochemistry, 66(12), 2537-2542 (2003-02-25)
Chemical regulation of secondary-metabolite synthesis was investigated through the improvement of poly-3-hydroxybutyrate (PHB) production in transgenic tobacco plants by the use of enzyme inhibitors. Two tobacco lines, BC3 and rCAB8, that produce PHB in both the cytosol and plastids were
Munees Ahemad et al.
Bulletin of environmental contamination and toxicology, 82(6), 761-766 (2009-03-18)
In modern conventional agriculture, herbicides are frequently used to prevent yield losses due to weeds. Herbicides also affect negatively the productivity of legumes. With these considerations, we evaluated the effects of soil applications of different concentrations of quizalafop-p-ethyl and clodinafop

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