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Dimethomorph

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C21H22ClNO4
CAS-Nummer:
110488-70-5
Molekulargewicht:
387.86
Beilstein:
8794474
EG-Nummer:
404-200-2
MDL-Nummer:
MFCD01632781
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329757062
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Beschreibung

mixture of E + Z isomers

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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+

InChIKey

QNBTYORWCCMPQP-NBVRZTHBSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Health hazardEnvironment
GHS08,GHS09

Signalwort

Danger

H-Sätze

H360F,H411

Gefahreneinstufungen

Aquatic Chronic 2 - Repr. 1B

Lagerklassenschlüssel

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

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCL0915
BCCC6295
BCBW7650
BCBS2582V
SZBE044XV

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Jianqiang Miao et al.
Pesticide biochemistry and physiology, 147, 96-101 (2018-06-24)
The novel fungicide oxathiapiprolin has potential for the control of downy mildew of cucumber, which is caused by Pseudoperonospora cubensis. In this study, an in vitro bioassay with detached leaves was used to determine the baseline sensitivity to oxathiapiprolin for
Hongwu Liang et al.
Ecotoxicology and environmental safety, 74(5), 1331-1335 (2011-03-26)
The dissipation and residual levels of dimethomorph in pepper and soil under field conditions were determined by gas chromatography with an electron capture detector (GC-ECD). The dissipation rates of dimethomorph were described using first-order kinetics and its half-life ranged from
Pieter Spanoghe et al.
Pest management science, 66(2), 126-131 (2009-09-12)
As part of ongoing research for a sustainable production of Belgian endives, the fate of three fungicides during storage, handling and forcing of witloof chicory roots was investigated. Storage roots are protected against Sclerotinia sp. Fuckel and Phoma exigua var.
M J Hengel et al.
Journal of agricultural and food chemistry, 48(12), 5824-5828 (2001-04-21)
An analytical method for the determination of dimethomorph [(E,Z)-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl]morpholine] residues in dried hops was developed utilizing liquid-liquid partitioning, automated gel permeation chromatography (GPC), Florisil and aminopropyl solid phase extraction (SPE) column cleanups, and gas chromatography (GC) with mass selective detection
L Y Fang et al.
Journal of capillary electrophoresis, 5(3-4), 115-123 (2000-05-08)
The feasibility of using capillary electrochromatography (CEC) as a high-efficiency reversed-phase separation technique has been demonstrated for the analysis of some pesticide formulation products. Some operating parameters of CEC analysis (organic modifier content, pH of the buffer, and sample diluent)
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