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45389

Supelco

Chloroxuron

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H15ClN2O2
CAS Number:
Molecular Weight:
290.74
Beilstein/REAXYS Number:
2814275
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

CN(C)C(=O)Nc1ccc(Oc2ccc(Cl)cc2)cc1

InChI

1S/C15H15ClN2O2/c1-18(2)15(19)17-12-5-9-14(10-6-12)20-13-7-3-11(16)4-8-13/h3-10H,1-2H3,(H,17,19)

Inchi Key

IVUXTESCPZUGJC-UHFFFAOYSA-N

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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.

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Legal Information

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

Pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Acute 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

>212.0 °F

flash_point_c

> 100 °C

ppe

Eyeshields, Faceshields, Gloves


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Determination of chloroxuron in strawberries using liquid chromatography with electron-capture detection.
F A Maris et al.
Bulletin of environmental contamination and toxicology, 35(6), 711-715 (1985-12-01)
A Amorisco et al.
Rapid communications in mass spectrometry : RCM, 20(10), 1569-1576 (2006-04-22)
The first stages of the photocatalytic degradation of the compounds chlortoluron [3-(3-chloro-4-methylphenyl)-1,1-dimethylurea] and chloroxuron [3-[4-(4-chlorophenoxy)phenyl]-1,1-dimethylurea], belonging to the class of phenyl-urea herbicides, were investigated using high-performance liquid chromatography (HPLC) coupled to electrospray ionization ion trap tandem mass spectrometry (ESI-IT-MS/MS). Degradation
C Yang et al.
Electrophoresis, 20(12), 2337-2342 (1999-09-28)
Capillary electrochromatography (CEC) was introduced to the separation of nine important urea herbicides using octadecyl-silica (ODS) capillary columns that were specially designed to allow the realization of a relatively strong electroosmotic flow (EOF) and, in turn, fast separations. The ODS

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