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45890

Supelco

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

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

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

Signal Word

Danger

Hazard Statements

H225,H304,H315,H336,H410

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 Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

-0.4 °F - closed cup

Flash Point(C)

-18 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD8855
BCBR5564V
SZBC172XV
SZB8163XV
SZE8163X

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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
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
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
Can mild organophosphate poisoning result in myocardial infarction?
Hossein Sanaei-Zadeh
Journal of forensic and legal medicine, 19(6), 363-363 (2012-08-01)
Meha Jaiswal et al.
Environmental science and pollution research international, 19(6), 2055-2062 (2012-01-05)
Removal of malathion from agricultural runoff was studied using novel copper-coated chitosan nanocomposite (CuCH)-a biopolymeric waste obtained from marine industry. Synthesis and characterization of the adsorbent using different spectral techniques like Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy, energy-dispersive
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