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Merck

45890

Parathion solution

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

Synonym(s):

Parathion-ethyl solution

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About This Item

Empirical Formula (Hill Notation):
C10H14NO5PS
CAS Number:
56-38-2
Molecular Weight:
291.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757002
MDL number:
MFCD00036219
Beilstein/REAXYS Number:
8912188

Product Name

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

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

InChI key

LCCNCVORNKJIRZ-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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

Quality Level

100

Related Categories

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

-0.4 °F - closed cup

flash_point_c

-18 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM7333
BCCD8855
BCBR5564V

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Becky J Proskocil et al.
American journal of physiology. Lung cellular and molecular physiology, 304(8), L519-L529 (2013-02-05)
Organophosphorus pesticides (OPs) are implicated in human asthma. We previously demonstrated that, at concentrations that do not inhibit acetylcholinesterase activity, the OP parathion causes airway hyperreactivity in guinea pigs as a result of functional loss of inhibitory M2 muscarinic receptors
Edibe Karasu-Minareci et al.
Journal of forensic and legal medicine, 19(2), 94-96 (2012-01-28)
The increase in accidental organophosphate poisoning as well as the rise in the number of cases of suicide attempts with organophosphate compounds is due to primarily to the widespread use of these compounds in agriculture. Organophosphates are anti-acetycholinesterase agents and
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
Organ donation following fatal organophosphate poisoning.
Jean-Louis Mariage et al.
Transplant international : official journal of the European Society for Organ Transplantation, 25(6), e71-e72 (2012-03-27)
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