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Supelco

Carpropamid

PESTANAL®, analytical standard

Sinônimo(s):

2,2-Dichloro-N-[1-(4-chlorophenyl)ethyl]-1-ethyl-3-methylcyclopropanecarboxamide

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About This Item

Fórmula empírica (Notação de Hill):
C15H18Cl3NO
Número CAS:
Peso molecular:
334.67
Beilstein:
8395957
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

formato

neat

cadeia de caracteres SMILES

CCC1(C(C)C1(Cl)Cl)C(=O)NC(C)c2ccc(Cl)cc2

InChI

1S/C15H18Cl3NO/c1-4-14(10(3)15(14,17)18)13(20)19-9(2)11-5-7-12(16)8-6-11/h5-10H,4H2,1-3H3,(H,19,20)

chave InChI

RXDMAYSSBPYBFW-UHFFFAOYSA-N

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Descrição geral

Carpropamid is widely used for the control of rice blast caused by Pyricularia oryzae. Carpropamid acts by inhibiting scytalone dehydratase enzyme involved in fungal melanin biosynthesis in a phytopathogenic fungus.

Aplicação

Carpropamid may be used as a reference standard for the determination of the analyte in river water by liquid chromatography/time-of-flight mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informações legais

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

Pictogramas

Environment

Frases de perigo

Declarações de precaução

Classificações de perigo

Aquatic Chronic 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Certificados de análise (COA)

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Tri Puji Priyatno et al.
TheScientificWorldJournal, 2012, 545784-545784 (2012-06-06)
The cyclic AMP- (cAMP-) dependent protein kinase A signaling pathway is one of the major signaling pathways responsible for regulation of the morphogenesis and pathogenesis of several pathogenic fungi. To evaluate the role of this pathway in the plant pathogenic
Cryogenic X-ray crystal structure analysis for the complex of scytalone dehydratase of a rice blast fungus and its tight-binding inhibitor, carpropamid: the structural basis of tight-binding inhibition.
Nakasako M, et al.
Biochemistry, 37(28), 9931- 9939 (1998)
Carpropamid: a rice fungicide with two modes of action.
Thieron M, et al.
Pflanzenschutz-Nachrichten Bayer, 51(28), 257- 278 (1998)
A new on-line sample preparation system for the liquid chromatography/time-of-flight mass spectrometry simultaneous analysis of pesticides in river water.
Sasaki H, et al.
Analytical Sciences, 22(6), 835- 840 (2006)
Young Seop Kwon et al.
Analytica chimica acta, 868, 60-66 (2015-03-31)
The sensitive detection of iprobenfos (IBF) and edifenphos (EDI) was successfully conducted by using a new aptamer-based colorimetric multi-aptasensor. The dissociation constants of this multi-target aptamer to both iprobenfos and edifenphos were found to be 1.67 μM and 38 nM

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