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Cyflumetofen

PESTANAL®, analytical standard

Synonym(s):

2-Methoxyethyl (RS)-2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-(α,α,α-trifluoro-o-tolyl)propionate

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About This Item

Empirical Formula (Hill Notation):
C24H24F3NO4
CAS Number:
Molecular Weight:
447.45
Beilstein:
11332768
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

COCCOC(=O)C(C#N)(C(=O)c1ccccc1C(F)(F)F)c2ccc(cc2)C(C)(C)C

InChI

1S/C24H24F3NO4/c1-22(2,3)16-9-11-17(12-10-16)23(15-28,21(30)32-14-13-31-4)20(29)18-7-5-6-8-19(18)24(25,26)27/h5-12H,13-14H2,1-4H3

InChI key

AWSZRJQNBMEZOI-UHFFFAOYSA-N

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General description

Cyflumetofen is an acaricide, which facilitates the rapid knockdown of spider mites and phytophagous mites. Its mode of action involves the inhibition of mitochondrial electron transport and is suitable for use in integrated pest management (IPM) systems.

Application

Cyflumetofen may be used as a reference standard for the determination of the analyte in samples of plant and animal origin using ultrahigh-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS).
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 hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2 - Skin Sens. 1A

Storage Class Code

11 - Combustible Solids

WGK

WGK 2


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Nena Pavlidi et al.
Insect biochemistry and molecular biology, 80, 101-115 (2016-12-10)
Cyflumetofen is a recently introduced acaricide with a novel mode of action, acting as an inhibitor of complex II of mitochondrial electron transport chain. It is activated by hydrolysis and the resulting de-esterified metabolite is a much stronger inhibitor. Cyflumetofen
Rui Quan et al.
Food chemistry, 321, 126687-126687 (2020-04-04)
The effect of food processing on the level and fate of chiral pesticide residues in apple products has rarely been investigated. In this study, we used ultra-performance convergence chromatography coupled with triple quadrupole mass spectrometry to determine the content of
Paul E Bergeron et al.
Pest management science, 76(6), 2170-2179 (2020-01-20)
Biological control in conventional agroecosystems involves the integration of chemical and conservation tactics, requiring knowledge of pesticide non-target effects on key natural enemies. Even for natural enemy groups such as predatory mites (Acari: Phytoseiidae), where pesticide non-target effects have been
Deng Pan et al.
Journal of economic entomology, 113(2), 918-923 (2019-12-11)
The citrus red mite, Panonychus citri (McGregor), is an important spider mite pest in citrus producing areas. Owing to long-term acaricide exposure, resistance has evolved rapidly in recent years. To evaluate the extent of resistance, seven field mite populations sampled
Wencai Lu et al.
Journal of economic entomology, 111(3), 1346-1353 (2018-03-01)
The carmine spider mite (Tetranychus cinnabarinus [Acarifonnes: Tetranychidae]) and the two-spotted spider mite (Tetranychus urticae [Acarifonnes: Tetranychidae]) are two notorious pests of agricultural crops. Control of these pests has been dependent upon using different kinds of acaricides. The purpose of

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