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Dimethomorph

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C21H22ClNO4
CAS Number:
Molecular Weight:
387.86
Beilstein:
8794474
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

description

mixture of E + Z isomers

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

SMILES string

COc1ccc(cc1OC)\C(=C\C(=O)N2CCOCC2)c3ccc(Cl)cc3

InChI

1S/C21H22ClNO4/c1-25-19-8-5-16(13-20(19)26-2)18(15-3-6-17(22)7-4-15)14-21(24)23-9-11-27-12-10-23/h3-8,13-14H,9-12H2,1-2H3/b18-14+

InChI key

QNBTYORWCCMPQP-NBVRZTHBSA-N

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General description

Dimethomorph, a cinnamic acid derivative, is a systemic morpholine fungicide mainly used against peronosporomycetes plant pathogens.

Application

Dimethomorph may be used as a reference standard for the determination of dimethomorph in dried hops by solvent extraction and liquid chromatography with ultraviolet detection (LC-UV).
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

Pictograms

Health hazardEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Chronic 2 - Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Rachel Dosnon-Olette et al.
The Science of the total environment, 408(10), 2254-2259 (2010-02-17)
Aquatic plants take up, transform and sequester organic contaminants and may therefore be used in phytoremediation for the removal of pollutants from wastewaters. A better understanding of factors affecting the rate of contaminant uptake by aquatic plants is needed to
Field optimization of dimethomorph for the control of potato late blight Phytophthora infestans: application rate, interval, and mixtures.
Stein J M and Kirk W W
Crop Protection, 22(4), 609-614 (2003)
Phototransformation pathways of the fungicide dimethomorph ((E, Z) 4-[3-(4-chlorophenyl)-3-(3, 4-dimethoxyphenyl)-1-oxo-2-propenyl] morpholine), relevant to sunlit surface waters.
Avetta P, et al.
The Science of the Total Environment, 500, 351-360 (2014)
Biological mode of action of dimethomorph on Pseudoperonospora cubensis and its systemic activity in cucumber.
Wang H-C, et al.
Agricultural sciences in China, 8(2), 172-181 (2009)
Jon W Wong et al.
Journal of agricultural and food chemistry, 52(21), 6361-6372 (2004-10-14)
A method was developed to determine pesticides in malt beverages using solid phase extraction on a polymeric cartridge and sample cleanup with a MgSO4-topped aminopropyl cartridge, followed by capillary gas chromatography with electron impact mass spectrometry in the selected ion

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