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Etofenprox

PESTANAL®, analytical standard

Synonym(s):

2-(4-Ethoxyphenyl)-2-methylpropyl 3-phenoxybenzyl ether

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About This Item

Empirical Formula (Hill Notation):
C25H28O3
CAS Number:
80844-07-1
Molecular Weight:
376.49
EC Number:
407-980-2
MDL number:
MFCD00210287
UNSPSC Code:
41116107
PubChem Substance ID:
329754810
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

CCOc1ccc(cc1)C(C)(C)COCc2cccc(Oc3ccccc3)c2

InChI

1S/C25H28O3/c1-4-27-22-15-13-21(14-16-22)25(2,3)19-26-18-20-9-8-12-24(17-20)28-23-10-6-5-7-11-23/h5-17H,4,18-19H2,1-3H3

InChI key

YREQHYQNNWYQCJ-UHFFFAOYSA-N

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General description

Etofenprox is a synthetic ether pyrethroidtype of insecticide, which can be used to control a broad spectrum of insects for agricultural purposes. It can be generally used to control insects like planthoppers and leafhoppers as well as insects, which show strong resistance towards organophosphorus and carbamate insecticides.

Application

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

Environment
GHS09

Signal Word

Warning

Hazard Statements

H362,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Lact.

Storage Class Code

11 - Combustible Solids

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)

Lot/Batch Number
BCCF8200
BCBT5101
SZBE265XV
SZBB101XV
SZB9216XV

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Guifang Jia et al.
Analytical and bioanalytical chemistry, 384(6), 1423-1427 (2006-02-24)
A method is described for determination of residues of the insecticide Etofenprox in environmental samples. Anionic surfactant micelle-mediated extraction (coacervation extraction) was evaluated for isolation of Etofenprox before HPLC. The optimum conditions used for extraction included: 0.09 g sodium dodecanesulfonate
Determination of Etofenprox in environmental samples by HPLC after anionic surfactant micelle-mediated extraction (coacervation extraction)
Jia G, et al.
Analytical and Bioanalytical Chemistry, 384, 1423-1427 (2006)
Xinya Liu et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1140, 121995-121995 (2020-02-15)
In this study, low-density deep eutectic solvent combined with dispersive liquid-liquid microextraction was applied to the extraction of five benzoylurea insecticides (BUs, including diflubenzuron, triflumuron, hexaflumuron, flufenoxuron, and chlorfluazuron) from beverages. Then the extracted and concentrated samples were analyzed and
Jian Wang et al.
Journal of AOAC International, 90(2), 550-567 (2007-05-04)
A liquid chromatography/electrospray ionization-tandem mass spectrometry (LC/ESI-MS/MS) method was developed and validated to determine 90 pesticides in apple samples. MS/MS data acquisition was achieved by applying multiple-reaction monitoring of 2 fragment ion transitions to provide a high degree of sensitivity
Aaron D Gross et al.
Insects, 9(4) (2018-10-27)
Anopheles gambiae Giles (Diptera: Culicidae) is the most prolific malaria vector in sub-Saharan Africa, where widespread insecticide resistance has been reported. An. gambiae laboratory strains are commonly used to study the basic biology of this important mosquito vector, and also
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