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MilliporeSigma

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
Beilstein/REAXYS Number:
8912188
MDL number:
MFCD00036219
UNSPSC Code:
41116107
PubChem Substance ID:
329757002
NACRES:
NA.24

Key Documents

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grade

analytical standard

Quality Level

100

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

SMILES string

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

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

InChI key

LCCNCVORNKJIRZ-UHFFFAOYSA-N

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_germany

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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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
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
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
Josef Seifert
Environmental toxicology and pharmacology, 35(2), 200-206 (2013-01-19)
This paper provides new information related to the mechanism of OPI (organophosphorus insecticides) teratogenesis. The COMFA (comparative molecular field analysis) and COMSIA (comparative molecular similarity indices analysis) suggest that the electrostatic and steric fields are the best predictors of OPI
View All Related Papers

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