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Merck

34326

Supelco

霜脲氰

PESTANAL®, analytical standard

别名:

1-(2-氰基-2-甲氧基亚氨基乙酰基)-3-乙基脲

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About This Item

经验公式(希尔记法):
C7H10N4O3
CAS号:
分子量:
198.18
Beilstein:
2214018
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

形式

neat

SMILES 字串

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 密鑰

XERJKGMBORTKEO-VZUCSPMQSA-N

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一般說明

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

應用

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.

注意

Sensitive, handle under inert gas.

法律資訊

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

訊號詞

Warning

危險分類

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

標靶器官

Blood,thymus

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

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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