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45651

Supelco

Quinalphos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C12H15N2O3PS
Número de CAS:
13593-03-8
Peso molecular:
298.30
Beilstein:
754823
Número CE:
237-031-6
Número MDL:
MFCD00078719
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329756865
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

CCOP(=S)(OCC)Oc1cnc2ccccc2n1

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

Clave InChI

JYQUHIFYBATCCY-UHFFFAOYSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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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.

Información legal

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

Palabra de señalización

Danger

Clasificaciones de peligro

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

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCK4704
BCCJ3460
BCCH1301
BCCB8533
BCBT9651

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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
Azim Haziq Zainuddin et al.
Environmental geochemistry and health, 42(11), 3703-3715 (2020-06-04)
The application of organophosphorus pesticides (OPPs) increased gradually because of the rise in global food demand that triggered the agriculture sector to increase the production, leading to OPP residues in the surface water. This study elucidated the presence of OPPs
L K S Chauhan et al.
Mutation research, 587(1-2), 120-125 (2005-09-28)
In vivo cytogenetic effects of commercially formulated cypermethrin (CYP, synthetic pyrethroid insecticide) and/or quinalphos (QUI, organophosphate insecticide), generally used in combination, were examined through chromosomal aberrations (CA) and micronucleus test (MT) in mice. Male mice were orally gavaged to a
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
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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Chromatograms

application for LC-MS, application for SPE

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