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Thiodicarb

PESTANAL®, analytical standard

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About This Item

Formule empirique (notation de Hill):
C10H18N4O4S3
Numéro CAS:
59669-26-0
Poids moléculaire :
354.47
Numéro CE :
261-848-7
Numéro MDL:
MFCD00145401
Code UNSPSC :
41116107
ID de substance PubChem :
329754970
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

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
GHS06,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301,H330,H400

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
BCCH8681
BCCH2352
BCBV7272
BCBT8119
BCBT7191

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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)
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)
H L Ammon et al.
Acta crystallographica. Section C, Crystal structure communications, 51 ( Pt 8), 1619-1621 (1995-08-15)
Dimethyl N,N'-[thiobis(methyliminocarbonyloxy)] bis-(ethanimidothiolate), C10H18N4O4S3, is an example of a sulfenylated biscarbamate insecticide. The molecule has an approximate twofold axis through the central S atom which joins the two methyliminocarbonyloxyethanimidothiolate units. One of the two arms is planar in the crystal.
Dislodgable insecticide residues on cotton foliage: acephate, AC 222,705, EPN, fenvalerate, methomyl, methyl parathion, permethrin, and thiodicarb.
G W Ware et al.
Bulletin of environmental contamination and toxicology, 25(4), 608-615 (1980-10-01)
M Q Yi et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 143(1), 113-116 (2006-02-08)
The inhibitory effects of four carbamate insecticides, methomyl, thiodicarb, carbofuran and carbosulfan, on acetylcholinesterase of male and female Carassius auratus were investigated in the laboratory. Kinetic constants, biomolecular rate constant (k(i)), carbamylation rate constant (k2) and decarbamylation rate constant (k3)
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