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Merck

45607

Parathion

PESTANAL®, analytical standard

Synonym(s):

O,O-Diethyl O-(4-nitrophenyl) phosphorothioate, Ethylparathione, Parathion-ethyl

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About This Item

Empirical Formula (Hill Notation):
C10H14NO5PS
CAS Number:
Molecular Weight:
291.26
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
200-271-7
MDL number:

Product Name

Parathion, PESTANAL®, analytical standard

InChI key

LCCNCVORNKJIRZ-UHFFFAOYSA-N

InChI

1S/C10H14NO5PS/c1-3-14-17(18,15-4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3

SMILES string

CCOP(=S)(OCC)Oc1ccc(cc1)[N+]([O-])=O

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

Quality Level

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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

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 1 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 1

Storage Class

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

wgk

WGK 3

flash_point_f

248.0 °F - closed cup

flash_point_c

120 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Heleni Tsoukali et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 822(1-2), 194-200 (2005-07-02)
Headspace-solid phase microextraction (HS-SPME) was studied and optimised for the determination of four common organophosphorus pesticides (OPPs) in biological samples. Various parameters controlling SPME were studied: choice of SPME fiber, type and content of salt added, preheating and extraction time
Rania Ibrahim et al.
International journal of pharmaceutics, 435(1), 33-37 (2012-04-10)
A previously developed method employing the use of a dialysis membrane in series with human dermis tissue mounted in side-by-side diffusion cells was utilized to observe the effects of the presence of soluble proteins in the donor compartment on the
Jerry Yen et al.
Neurotoxicology and teratology, 33(6), 735-741 (2011-11-01)
Zebrafish are increasingly used for developmental neurotoxicity testing because early embryonic events are easy to visualize, exposures are done without affecting the mother and the rapid development of zebrafish allows for high throughput testing. We used zebrafish to examine how
Abdul Shafeeuulla Khan et al.
Journal of molecular graphics & modelling, 34, 10-17 (2012-02-07)
The extreme toxicity of organophosphorus nerve agents and pesticides mandates to employ models or simulants in place of the actual compounds in the laboratory. The importance of simulants is known, however, their efficacy for direct comparison with the toxic organophosphorus
Basma Damiri et al.
Toxicological sciences : an official journal of the Society of Toxicology, 125(2), 368-381 (2011-11-16)
There are few in vivo knockout models available to study the function of Cyp2 members involved in the metabolism of endogenous and exogenous chemicals. These models may help provide insight into the cytochrome P450s (CYPs) responsible for the detoxification and

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