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34326

Supelco

Cymoxanil

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C7H10N4O3
CAS Number:
Molecular Weight:
198.18
Beilstein:
2214018
EC Number:
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

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+

InChI key

XERJKGMBORTKEO-VZUCSPMQSA-N

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General description

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

Application

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.

Caution

Sensitive, handle under inert gas.

Legal Information

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

Signal Word

Warning

Hazard Classifications

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

Target Organs

Blood,thymus

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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Customers Also Viewed

Sensitivity to cymoxanil in populations of Plasmopara viticola in northern Italy.
Gullino ML, et al.
Plant Pathology, 46(5), 729-736 (1997)
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)
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)
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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