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Supelco

Carpropamid

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C15H18Cl3NO
Numero CAS:
Peso molecolare:
334.67
Beilstein:
8395957
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

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)
RXDMAYSSBPYBFW-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

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.

Note legali

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

Pittogrammi

Environment

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Aquatic Chronic 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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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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