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Merck
CN

34326

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
261-043-0
Beilstein/REAXYS Number:
2214018
MDL number:
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InChI key

XERJKGMBORTKEO-VZUCSPMQSA-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+

SMILES string

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

grade

analytical standard

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

Quality Level

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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.

Legal Information

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

Disclaimer

Sensitive, handle under inert gas.

signalword

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

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

农药列管产品
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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)
Frédérique Tellier et al.
Pest management science, 65(2), 129-136 (2008-10-28)
The metabolism of cymoxanil [1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea] and fungicidal cyanooxime analogues was monitored on three phenotypes of Botrytis cinerea Pers. ex Fr. differing in their sensitivity towards cymoxanil. For this purpose, labelled [2-(14)C]cymoxanil was added either to the culture medium of these
Teratological examination of the experimental fungicide DPX 3217 50 WP in CFY rats.
L Várnagy et al.
Acta veterinaria Academiae Scientiarum Hungaricae, 28(2), 223-231 (1980-01-01)
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)

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