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Clothianidin

PESTANAL®, analytical standard

Synonym(s):

(E)-1-(2-Chloro-5-thiazolylmethyl)-3-methyl-2-nitroguanidine

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About This Item

Empirical Formula (Hill Notation):
C6H8ClN5O2S
CAS Number:
Molecular Weight:
249.68
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

CN\C(NCc1cnc(Cl)s1)=N/[N+]([O-])=O

InChI

1S/C6H8ClN5O2S/c1-8-6(11-12(13)14)10-3-4-2-9-5(7)15-4/h2H,3H2,1H3,(H2,8,10,11)

InChI key

PGOOBECODWQEAB-UHFFFAOYSA-N

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General description

Clothianidin is a neonicotinoid insecticide with excellent systemic action for a wide variety of insect pests, that acts effectively on nicotinic acetylcholine receptors (nAChR).
Find more information here: Neonicotinoids

Application

Clothianidin may be used as a reference standard for the analysis of the analyte in agricultural samples using dual-labeled time-resolved fluoro-immunoassay (TRFIA), followed by gas chromatography (GC).
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

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Description
Pricing

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Dual-labeled time-resolved fluoroimmunoassay for simultaneous detection of clothianidin and diniconazole in agricultural samples.
Sheng E, et al.
Food Chemistry, 192(2), 525-530 (2016)
Ni Xiang et al.
PloS one, 12(7), e0181201-e0181201 (2017-07-14)
Heterodera glycines, the soybean cyst nematode, is the most economically important plant-parasitic nematode on soybean production in the U.S. The objectives of this study were to evaluate the potential of plant growth-promoting rhizobacteria (PGPR) strains for mortality of H. glycines
H Hesketh et al.
Scientific reports, 6, 37655-37655 (2016-12-21)
Concern over reported honeybee (Apis mellifera spp.) losses has highlighted chemical exposure as a risk. Current laboratory oral toxicity tests in A. mellifera spp. use short-term, maximum 96 hour, exposures which may not necessarily account for chronic and cumulative toxicity. Here
Julia C Jones et al.
Ecology and evolution, 8(1), 441-451 (2018-01-13)
There is growing recognition that the gut microbial community regulates a wide variety of important functions in its animal hosts, including host health. However, the complex interactions between gut microbes and environment are still unclear. Honey bees are ecologically and
Antoine Abrieux et al.
PloS one, 11(11), e0167469-e0167469 (2016-12-03)
Neonicotinoid insecticides are widely used to protect plants against pest insects, and insecticide residues remaining in the environment affect both target and non-target organisms. Whereas low doses of neonicotinoids have been shown to disturb the behaviour of pollinating insects, recent

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

Protocols

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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