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Merck

36187

Supelco

Parathionmethyl

PESTANAL®, analytical standard

Synonym(e):

O,O-Dimethyl-O-(4-nitrophenyl)-phosphorothioat, Methyl-parathion

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About This Item

Empirische Formel (Hill-System):
C8H10NO5PS
CAS-Nummer:
Molekulargewicht:
263.21
Beilstein:
8905814
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

2-8°C

SMILES String

COP(=S)(OC)Oc1ccc(cc1)[N+]([O-])=O

InChI

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

InChIKey

RLBIQVVOMOPOHC-UHFFFAOYSA-N

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Allgemeine Beschreibung

Parathion-methyl is an organophosphorus insecticide and acaricide, which is widely used in controlling insect pests of agricultural crops, fruits and vegetables.

Anwendung

Parathion-methyl may be used as a reference standard in the determination of parathion-methyl in water samples using high performance liquid chromatography with electrochemical detection (HPLC-EC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Rechtliche Hinweise

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

Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 3 - STOT RE 2

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

114.8 °F - open cup

Flammpunkt (°C)

46 °C - open cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Analysenzertifikate (COA)

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Comparative study of three immunoassays based on monoclonal antibodies for detection of the pesticide parathion-methyl in real samples.
KolosovaY A, et al.
Analytica Chimica Acta, 511(2), 323-331 (2004)
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
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.
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
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

Protokolle

Test your food for fipronil contamination using our analytical standards, certified reference materials, solvents, and columns for analysis.

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