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Documentos Principais

33897

Supelco

Thiacloprid-amide

PESTANAL®, analytical standard

Sinônimo(s):

[3-(6-Chloro-3-pyridylmethyl)thiazolidin-2-ylidene]urea

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About This Item

Fórmula empírica (Notação de Hill):
C10H11ClN4OS
Número CAS:
Peso molecular:
270.74
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

Formato

neat

cadeia de caracteres SMILES

NC(=O)\N=C1/SCCN1Cc2ccc(Cl)nc2

InChI

1S/C10H11ClN4OS/c11-8-2-1-7(5-13-8)6-15-3-4-17-10(15)14-9(12)16/h1-2,5H,3-4,6H2,(H2,12,16)/b14-10-

chave InChI

LEZHOZPJYAQQNU-UVTDQMKNSA-N

Descrição geral

Thiacloprid-amide is a metabolite of thiacloprid, an insecticide belonging to the class of neonicotinoids.[1] It is primarily used for foliar applications for pest control in arable crops, orchards, vegetables, and other crops.[1]

Find more information here: Neonicotinoids

Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Thiacloprid-amide may be used as an analytical reference standard for the determination of the analyte in:
  • Green pepper/tomato samples using water based extraction and solid-phase extraction followed by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS).[2]
  • Honey bees and honey samples using solid-phase extraction followed by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS).[3]

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informações legais

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Certificados de análise (COA)

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Water-based extraction and liquid chromatography-tandem mass spectrometry analysis of neonicotinoid insecticides and their metabolites in green pepper/tomato samples.
Iwafune T, et al.
Journal of Agricultural and Food Chemistry, 62(13), 2790-2796 (2014)
Performance of honey bee colonies under a long-lasting dietary exposure to sublethal concentrations of the neonicotinoid insecticide thiacloprid.
Siede R, et al.
Pest Management Science, 73(7), 1334-1344 (2017)
Determination of neonicotinoid insecticides and their metabolites in honey bee and honey by liquid chromatography tandem mass spectrometry.
Gbylik-Sikorska M, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 990(7), 132-140 (2015)
Kouji H Harada et al.
PloS one, 11(1), e0146335-e0146335 (2016-01-06)
Neonicotinoids, which are novel pesticides, have entered into usage around the world because they are selectively toxic to arthropods and relatively non-toxic to vertebrates. It has been suggested that several neonicotinoids cause neurodevelopmental toxicity in mammals. The aim was to
Marc Le Vée et al.
Journal of biochemical and molecular toxicology, 33(10), e22379-e22379 (2019-08-01)
The interactions of six neonicotinoid pesticides and one neonicotinoid metabolite with drug transporters have been characterized in vitro. Acetamiprid, clothianidin, imidacloprid, nitenpyram, thiacloprid and its metabolite thiacloprid amide, and thiamethoxam, each used at 100 µM, did not impair activity of the

Protocolos

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

Analysis of banned neonicotinoid insecticides from dandelion blossoms using QuEChERS and LC-MS.

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