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Key Documents

32499

Supelco

Dinotefuran

PESTANAL®, analytical standard

Sinonimo/i:

(RS)-N-Methyl-N′-nitro-N″-[(tetrahydro-3-furanyl)methyl]guanidine

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About This Item

Formula empirica (notazione di Hill):
C7H14N4O3
Numero CAS:
Peso molecolare:
202.21
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

CN\C(N[N+]([O-])=O)=N/CC1CCOC1

InChI

1S/C7H14N4O3/c1-8-7(10-11(12)13)9-4-6-2-3-14-5-6/h6H,2-5H2,1H3,(H2,8,9,10)
YKBZOVFACRVRJN-UHFFFAOYSA-N

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Descrizione generale

Dinotefuran, a new neonicotinoid insecticide has low mammalian toxicity and great insecticidal activity against a broad range of pests.
Find more information here: Neonicotinoids

Applicazioni

Dinotefuran has been used as a standard for the determination of neonicotinoid insecticide residues in dietary bee pollen and melon samples by HPLC–MS/MS and high performance liquid chromatography coupled with ultraviolet detector (HPLC-UVD), respectively.
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

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Eiki Watanabe et al.
Talanta, 84(4), 1107-1111 (2011-05-03)
The analytical performance of a kit-based enzyme-linked immunosorbent assay (ELISA) for the determination of a neonicotinoid insecticide dinotefuran residue in rice samples is addressed. The sensitivity (I(50) value) was 5.4 ng/mL, with the limit of detection, 0.6 ng/mL and the
Md Musfiqur Rahman et al.
Food chemistry, 136(2), 1038-1046 (2012-11-06)
A new analytical method was developed for dinotefuran and its metabolites, MNG, UF, and DN, in melon using high-performance liquid chromatography (HPLC) coupled with an ultraviolet detector (UVD). Due to shorter wavelength, lower sensitivity to UV detection, and high water
XiaoBin Shi et al.
Pest management science, 67(12), 1528-1533 (2011-06-30)
Imidacloprid has been a major neonicotinoid insecticide for controlling Aphis gossypii (Glover) (Homoptera: Aphididae) and other piercing-sucking pests. However, the resistance to imidacloprid has been recorded in many target insects. At the same time, cross-resistance of imidacloprid and other insecticides
Raymond A Cloyd et al.
Pest management science, 67(1), 3-9 (2010-08-20)
The neonicotinoid insecticides imidacloprid, acetamiprid, dinotefuran, thiamethoxam and clothianidin are commonly used in greenhouses and/or interiorscapes (plant interiorscapes and conservatories) to manage a wide range of plant-feeding insects such as aphids, mealybugs and whiteflies. However, these systemic insecticides may also
The discovery of dinotefuran: a novel neonicotinoid.
Wakita T, et al.
Pest Management Science, 59(9), 1016-1022 (2003)

Articoli

Determination of Neonicotinoids in Honey using a Chromolith RP-18 HPLC column and UV Detection

Protocolli

Extraction and Analysis of Neonicotinoid Pesticides from Flower Blossoms Using Supel QuE and Ascentis® Express

LC/MS/MS Analysis of Neonicotinoid Pesticides in Dandelion Blossoms on Ascentis® Express C18 after Dispersive SPE (QuEChERS) using Supel™ QuE

Learn more about Neonicotinoids - active substances used in plant protection products to control harmful insects.

On Friday, April 27, 2018, the European Union decided to ban the use of three neonicotinoid insecticides from use on field crops, having deemed them dangerous to bees. This application demonstrates the analysis of these banned compounds and others from dandelion blossoms using QuEChERS and LC-MS.

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