31682
Carpropamid
PESTANAL®, analytical standard
Synonym(s):
2,2-Dichloro-N-[1-(4-chlorophenyl)ethyl]-1-ethyl-3-methylcyclopropanecarboxamide
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About This Item
Empirical Formula (Hill Notation):
C15H18Cl3NO
CAS Number:
Molecular Weight:
334.67
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8395957
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)
SMILES string
CCC1(C(C)C1(Cl)Cl)C(=O)NC(C)c2ccc(Cl)cc2
InChI key
RXDMAYSSBPYBFW-UHFFFAOYSA-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
Related Categories
General description
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.
Application
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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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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