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Documenti fondamentali

34094

Supelco

Etofenprox

PESTANAL®, analytical standard

Sinonimo/i:

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

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula empirica (notazione di Hill):
C25H28O3
Numero CAS:
Peso molecolare:
376.49
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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
YREQHYQNNWYQCJ-UHFFFAOYSA-N

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Descrizione generale

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.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

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

Pittogrammi

Environment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Lact.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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Certificati d'analisi (COA)

Lot/Batch Number

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Takamitsu Otake et al.
Journal of agricultural and food chemistry, 57(18), 8208-8212 (2009-08-26)
Brown rice powder certified reference material, NMIJ CRM 7504-a, for the analysis of pesticide residues was developed by the National Metrology Institute of Japan, part of the National Institute of Advanced Industrial Science and Technology. Brown rice sample was harvested
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
Martice E Vasquez et al.
Pest management science, 66(1), 28-34 (2009-08-18)
The pyrethroid insecticide etofenprox is of current interest to rice farmers in the Sacramento Valley owing to its effectiveness against the rice water weevil, Lissorhoptrus oryzophilus Kuschel. This study aimed to describe the partitioning of etofenprox under simulated rice field

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