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34074

Supelco

Quizalofop-P-ethyl

PESTANAL®, analytical standard

Synonyme(s) :

DPX-Y6202, Ethyl (R)-2-[4-(6-chloro-2-quinoxalyloxy)phenoxy]propionate, Quinofop-ethyl

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About This Item

Formule empirique (notation de Hill):
C19H17ClN2O4
Numéro CAS:
Poids moléculaire :
372.80
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

CCOC(=O)[C@@H](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/t12-/m1/s1

Clé InChI

OSUHJPCHFDQAIT-GFCCVEGCSA-N

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Description générale

Quizalofop-p-ethyl is a post-emergence herbicide, which belongs to the aryloxyphenoxypropionate group of herbicides. It commonly finds applications in annual and perennial weed control management.

Application

Quizalofop-p-ethyl may be used as a reference standard in determining the quizalofop-p-ethyl content in water and soil samples using enzyme-linked immunosorbent assay technique (ELISA).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informations légales

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

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

>212.0 °F - closed cup

Point d'éclair (°C)

> 100 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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Wen Chen et al.
Pest management science, 76(11), 3800-3805 (2020-06-02)
Asia minor bluegrass (Polypogon fugax) is one of the main weeds invading Chinese canola fields. The P. fugax resistant population SC-R, which survived quizalofop-p-ethyl at the field-recommended rate (67.5 g ha-1 ), was collected from a canola field in Qingsheng County
Quantitative determination of 8-hydroxyguanine and guanine by isotope dilution mass spectrometry.
Hamberg M and Zhang Y-L.
Analytical Biochemistry, 229(2), 336-344 (1995)
Delkin O Gonzalez et al.
BMC plant biology, 18(1), 14-14 (2018-01-18)
Availability of well characterized maize regulatory elements for gene expression in a variety of tissues and developmental stages provides effective alternatives for single and multigene transgenic concepts. We studied the expression of the herbicide tolerance gene aryloxyalkanoate dioxygenase (aad-1) driven
Shuo Wang et al.
Bulletin of environmental contamination and toxicology, 105(4), 602-606 (2020-09-27)
A method for simultaneous quantitation of rimsulfuron, quizalofop-P-ethyl and quizalofop-P in potato plant, soil and potato tuber samples was established. The mean recoveries of rimsulfuron, quizalofop-P-ethyl and quizalofop-P in different matrices spiked with them were 81.4%-101.1%, 76.1%-99.0% and 77.4%-106.4% with
S K Sahoo et al.
Environmental monitoring and assessment, 185(2), 1711-1718 (2012-05-11)
Quizalofop ethyl, a phenoxy propionate herbicide, is used for postemergence control of annual and perennial grass weeds in broad-leaved crops in India. The experiments were designed to study the dissipation kinetics of quizalofop ethyl on onion for two seasons. A

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