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Merck

32499

Supelco

Dinotefuran

PESTANAL®, analytical standard

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C7H14N4O3
Número de CAS:
Peso molecular:
202.21
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

formato

neat

cadena SMILES

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)

Clave InChI

YKBZOVFACRVRJN-UHFFFAOYSA-N

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Descripción general

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

Aplicación

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.

Información legal

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

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Eye Irrit. 2

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Certificados de análisis (COA)

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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
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)
Frank J Byrne et al.
Pest management science, 63(9), 860-866 (2007-07-27)
The efficacies of four systemic neonicotinoid insecticides applied to potted avocado trees at manufacturer-recommended rates were assessed against the avocado thrips, Scirtothrips perseae Nakahara. At the time of treatment, fully expanded first-flush young leaves were tagged for identification, and a

Artículos

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

Protocolos

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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