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Merck
CN

45651

Quinalphos

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H15N2O3PS
CAS Number:
13593-03-8
Molecular Weight:
298.30
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756865
EC Number:
237-031-6
Beilstein/REAXYS Number:
754823
MDL number:
MFCD00078719

Key Documents

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InChI key

JYQUHIFYBATCCY-UHFFFAOYSA-N

InChI

1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-12-9-13-10-7-5-6-8-11(10)14-12/h5-9H,3-4H2,1-2H3

SMILES string

CCOP(=S)(OCC)Oc1cnc2ccccc2n1

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
environmental

format

neat

storage temp.

2-8°C

Quality Level

100

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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.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

危险化学品
农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCP0225
BCCK4704
BCCJ3460
BCCH1301
BCCB8533

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Bárbara Reichert et al.
Analytica chimica acta, 1004, 40-50 (2018-01-14)
This paper describes the optimization and validation of an acetonitrile based method for simultaneous extraction of multiple pesticides and mycotoxins from raw coffee beans followed by LC-ESI-MS/MS determination. Before extraction, the raw coffee samples were milled and then slurried with
Vijay A K B Gundi et al.
Ecotoxicology and environmental safety, 68(2), 278-285 (2007-02-06)
Interaction effects of the insecticides monocrotophos and quinalphos (organophosphates), and cypermethrin (pyrethroid), on microbial activities in two agricultural soils-black vertisol soil and red alfinsol soil were tested for 30 days under laboratory conditions. Individual application of the three insecticides at
C Gonçalves et al.
Chemosphere, 64(8), 1375-1382 (2006-02-14)
The photochemical persistence of quinalphos, one of the most widely used organophosphorous insecticides, was investigated in a variety of environmental matrices such as natural waters and soils of different composition. Simulated solar irradiation was obtained using a xenon arc lamp
Sushma Pandey et al.
Chemosphere, 63(5), 869-880 (2005-10-01)
Chlorpyrifos (O,O-diethyl O-3,5,6-trichloro-2 pyridyl phosphorothioate) 20 EC and Quinalphos (O,O-diethyl O-quinoxalin-2-yl phosphorothioate) 25 EC, were applied in groundnut (Arachis hypogaea L.) field as seed treatment at 25 ml/kg and soil treatment at 4 l/ha in 1998 and 1999. The residues
M Azharul Islam et al.
Journal of hazardous materials, 170(1), 230-238 (2009-05-30)
This paper deals with the multiple response optimization for the removal of organophosphorus pesticide quinalphos [QP: O,O-diethyl O-2-quinoxalinyl phosphorothioate] from the aqueous solution onto low-cost material and tried to overcome the drawbacks of univariate optimization. Used tea leaves were used
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