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36158

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Methidathion

PESTANAL®, analytical standard

Synonym(s):

S-2,3-Dihydro-5-methoxy-2-oxo-1,3,4-thiodiazol-3-yl-methyl-O,O-dimethyl-phosphodithioate

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About This Item

Empirical Formula (Hill Notation):
C6H11N2O4PS3
CAS Number:
950-37-8
Molecular Weight:
302.33
Beilstein:
619915
EC Number:
213-449-4
MDL number:
MFCD00055286
UNSPSC Code:
41116107
PubChem Substance ID:
329755304
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

storage temp.

2-8°C

SMILES string

COC1=NN(CSP(=S)(OC)OC)C(=O)S1

InChI

1S/C6H11N2O4PS3/c1-10-5-7-8(6(9)16-5)4-15-13(14,11-2)12-3/h4H2,1-3H3

InChI key

MEBQXILRKZHVCX-UHFFFAOYSA-N

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General description

Methidathion is a dimethoxyorganic phosphorus pesticide and cholinesterase inhibitor.

Application

Methidathion may be used as a reference standard for the determination of methidathion in serum and urine samples of acute poisoning by high-performance liquid chromatography with diode-array detector.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

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
BCCJ3747
BCBX1633
SZBD234XV
SZBB174XV
SZB7263XV

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Evaluation of the carcinogenic potential of pesticides: 2. Methidathion.
Quest J A, et al.
Regulatory Toxicology and Pharmacology, 12(2), 117-126 (1990)
Determination of organophosphorus pesticides in biological samples of acute poisoning by HPLC with diode-array detector.
Cho Y, et al.
Chemical & Pharmaceutical Bulletin, 45(4), 737-740 (1997)
Thai-Hoang Le et al.
Chemosphere, 79(1), 67-71 (2010-01-26)
In this study, the expression of five stress responsive genes was quantified and analyzed using a semi-quantitative RT-PCR to study the changes in their expression in Daphnia magna after exposure to known pesticides, glyphosate and methidathion. Hemoglobin (Dhb), which was
Eloisa Caldas et al.
Food additives and contaminants, 23(2), 148-158 (2006-02-02)
Field trials were conducted in commercial agricultural areas in Brazil to determine the variability of residues of parathion methyl, diazinon and methidathion in individual units of large crops treated twice with a mixture of the three pesticides. Over 120 random
Idriss Bakas et al.
Analytica chimica acta, 734, 99-105 (2012-06-19)
A specific adsorbent for extraction of methidathion from olive oil was developed. The design of the molecularly imprinted polymer (MIP) was based on the results of the computational screening of the library of polymerisable functional monomers. MIP was prepared by
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