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Key Documents

34326

Supelco

Cymoxanil

PESTANAL®, analytical standard

Sinonimo/i:

1-(2-Cyano-2-methoxyiminoacetyl)-3-ethylurea

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About This Item

Formula empirica (notazione di Hill):
C7H10N4O3
Numero CAS:
Peso molecolare:
198.18
Beilstein:
2214018
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

CCNC(=O)NC(=O)C(=N\OC)\C#N

InChI

1S/C7H10N4O3/c1-3-9-7(13)10-6(12)5(4-8)11-14-2/h3H2,1-2H3,(H2,9,10,12,13)/b11-5+
XERJKGMBORTKEO-VZUCSPMQSA-N

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Descrizione generale

Cymoxanil is an agricultural fungicide effective against Peronosporales fungus affecting fruits and vegetables.

Applicazioni

Cymoxanil may be used as an analytical reference standard for the determination of the analyte in foodstuffs, soil, commercial pesticide formulation and tobacco by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Avvertenza

Sensitive, handle under inert gas.

Note legali

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

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1 - STOT RE 2

Organi bersaglio

Blood,thymus

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Certificati d'analisi (COA)

Lot/Batch Number

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Rapid determination of famoxadone and cymoxanil in commercial pesticide formulation by high performance liquid chromatography using a C18 monolithic rod column.
Balayiannis G, et al.
Bulletin of Environmental Contamination and Toxicology, 93(6), 775-780 (2014)
Determination of simazine and cymoxanil in soils by microwave-assisted solvent extraction and HPLC with reductive amperometrical detection.
de Sabando OL, et al.
Chromatographia, 55(11-12), 667-671 (2002)
Sensitivity to cymoxanil in populations of Plasmopara viticola in northern Italy.
Gullino ML, et al.
Plant Pathology, 46(5), 729-736 (1997)
Frederique Tellier et al.
Journal of agricultural and food chemistry, 56(17), 8050-8057 (2008-08-13)
The metabolism of cymoxanil [1-(2-cyano-2-methoxyiminoacetyl)-3-ethyl urea] by a very sensitive strain of Botrytis cinerea toward this fungicide was studied by using [2-(14)C]-cymoxanil. Labeled cymoxanil was added either in a culture of this strain or in its enzymatic extract. The main
W Lindner et al.
Zeitschrift fur Lebensmittel-Untersuchung und -Forschung, 178(6), 471-474 (1984-06-01)
Residues of the contact fungicide Cymoxanil in grapes were determined by a multidimensional multicolumn high pressure liquid chromatography technique (MC-HPLC). The sample pretreatment is a simple water extraction. Further clean-up and trace enrichment of an aliquot of the aqueous acidic

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