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Merck
CN

45891

Parathion-methyl solution

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:
298-00-0
Molecular Weight:
263.21
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757003
MDL number:
MFCD00041813
Beilstein/REAXYS Number:
8905814

Key Documents

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InChI

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

SMILES string

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

InChI key

RLBIQVVOMOPOHC-UHFFFAOYSA-N

grade

analytical standard

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

Quality Level

100

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

signalword

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

WGK 2

flash_point_f

-4.0 °F - closed cup

flash_point_c

-20 °C - closed cup

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCC3581
BCBT4026

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Scott A Trammell et al.
Chemical communications (Cambridge, England), 48(34), 4121-4123 (2012-03-22)
Using a low power green laser, we have demonstrated a rate acceleration of ~2-fold for the hydrolysis of methyl parathion by irradiating the plasmon absorption band of Au nanoparticles capped with a Cu(bpy) catalyst.
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
Xiang Huang et al.
Aquatic toxicology (Amsterdam, Netherlands), 114-115, 189-199 (2012-03-27)
Methyl parathion (MP) is a widely used organophosphorus pesticide that causes severe health and environmental effects. We investigated the alteration of the proteomic profile in the membrane enriched fraction of the kidneys of the scallop Mizuhopecten yessoensis exposed to low-level
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
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