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Thiodicarb

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H18N4O4S3
CAS Number:
59669-26-0
Molecular Weight:
354.47
EC Number:
261-848-7
MDL number:
MFCD00145401
UNSPSC Code:
41116107
PubChem Substance ID:
329754970
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H330,H400

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH8681
BCCH2352
BCBV7272
BCBT8119
BCBT7191

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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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