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45891

Supelco

Parathion-methyl solution

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100 μg/mL in cyclohexane, PESTANAL®, analytical standard

Synonym(s):

Methyl parathion

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About This Item

Empirical Formula (Hill Notation):
C8H10NO5PS
CAS Number:
Molecular Weight:
263.21
Beilstein/REAXYS Number:
8905814
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in cyclohexane

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

single component solution

storage temp.

2-8°C

SMILES string

S=P(OC)(OC)OC1=CC=C([N+]([O-])=O)C=C1

InChI

1S/C8H10NO5PS/c1-12-15(16,13-2)14-8-5-3-7(4-6-8)9(10)11/h3-6H,1-2H3

InChI key

RLBIQVVOMOPOHC-UHFFFAOYSA-N

Application

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

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Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

-4.0 °F - closed cup

flash_point_c

-20 °C - closed cup


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Thiago M R Araújo et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 48(4), 251-259 (2013-02-05)
This work presents a study of the abiotic degradation of commercially available methyl parathion in aqueous solution at two different concentrations (88 mg/L and 200 μg/L). The effects of solar irradiation and the presence of humic acids were evaluated and
Jingming Gong et al.
Biosensors & bioelectronics, 39(1), 320-323 (2012-08-08)
We developed a highly sensitive flow injection/amperometric biosensor for the detection of organophosphate pesticides (OPs) using layered double hydroxides (LDHs) as the immobilization matrix of acetylcholinesterase (AChE). LDHs provided a biocompatible microenvironment to keep the bioactivity of AChE, due to
Anirut Ekkhunnatham et al.
World journal of microbiology & biotechnology, 28(4), 1739-1746 (2012-07-19)
Methyl parathion hydrolase (MPH) from a methyl parathion-degrading Burkholderia cepacia indigenous to Thailand was purified to apparent homogeneity by three steps of column chromatography using Resource S, Sephadex G100, and Octyl Sepharose 4FF columns. Its molecular mass was determined to
Mohamed Abdel-Razek Saleh Abdel-Razek et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 48(6), 449-461 (2013-03-05)
The goal of this study was to optimize methyl parathion (O,O-dimethyl-O-4-p-nitrophenyl phosphorothioate) degradation using a strain of Escherichia coli DH5α expressing the opd gene. Our results indicate that this strain had lower enzymatic activity compared to the Flavobacterium sp. ATCC
Neetu Tiwari et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 101, 54-58 (2012-10-27)
A new selective and sensitive kinetic method has been developed for spectrophotometric determination of methyl parathion based on its inhibitory effect on the redox reaction between bromate and hydrochloric acid. The decolorization of neutral red by the reaction product was

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