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Merck

32499

Supelco

Dinotefuran

PESTANAL®, analytical standard

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C7H14N4O3
CAS-Nummer:
Molekulargewicht:
202.21
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

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

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)

InChIKey

YKBZOVFACRVRJN-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

Lot/Batch Number

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Kunden haben sich ebenfalls angesehen

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)

Artikel

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

Protokolle

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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