All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C10H18N4O4S3
CAS Number:
Molecular Weight:
354.47
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
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
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-
InChI key
XDOTVMNBCQVZKG-OXAWKVHCSA-N
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General description
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.
Recommended products
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
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
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
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