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Thiodicarb

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C10H18N4O4S3
Numéro CAS:
Poids moléculaire :
354.47
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

CS\C(C)=N/OC(=O)N(C)SN(C)C(=O)O\N=C(\C)SC

InChI

1S/C10H18N4O4S3/c1-7(19-5)11-17-9(15)13(3)21-14(4)10(16)18-12-8(2)20-6/h1-6H3/b11-7-,12-8-

Clé InChI

XDOTVMNBCQVZKG-OXAWKVHCSA-N

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Description générale

Thiodicarb is a carbamate herbicide effective against Lepidoptera, Coleoptera, Diptera and Hemiptera pests. It acts by inhibiting acetylcholinesterase activity.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Thiodicarb may be used as an analytical reference standard for the determination of the analyte in cotton, fruits/vegetables, and in different food matrices by various chromatography techniques.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Skull and crossbonesEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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Determination of carbamate pesticide residues in vegetables and fruits by liquid chromatography- atmospheric pressure photoionization- mass spectrometry and atmospheric pressure chemical ionization- mass spectrometry.
Takino M, et al.
Journal of Agricultural and Food Chemistry, 52(4), 727-735 (2004)
Simultaneous determination of thiodicarb and its main metabolite residues in cotton by ultra-performance liquid chromatography coupled to tandem mass spectrometry.
Wu Y, et al.
Analytical Methods : Advancing Methods and Applications, 5(4), 1052-1057 (2013)
C L Lanning et al.
Toxicology letters, 85(3), 127-133 (1996-06-01)
Pesticides have been shown to interact with the multidrug resistance protein associated with cancer chemotherapy, P-glycoprotein (P-gp). P-gp, therefore, has also been implicated in the development of pesticide resistance. The purpose of this study was to characterize the effect P-gp
C P Suh et al.
Journal of economic entomology, 93(3), 577-583 (2000-07-21)
The effect of insecticides on Trichogramma exiguum Pinto & Platner emergence, adult survival, and fitness parameters was investigated. Insecticides tested were lambda cyhalothrin, cypermethrin, thiodicarb, profenophos, spinosad, methoxyfenozide, and tebufenozide. All insecticides, with the exception of methoxyfenozide and tebufenozide, adversely
Sally K Moccelini et al.
Talanta, 82(1), 164-170 (2010-08-06)
A biosensor based on alfalfa sprout (Medicago sativa) homogenate as a source of peroxidase is proposed for the determination of thiodicarb by square-wave voltammetry. This enzyme was immobilized in self-assembled monolayers of l-cysteine on a gold electrode. Several parameters were

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