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36164

Supelco

Metoxuron

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H13ClN2O2
CAS Number:
Molecular Weight:
228.68
Beilstein:
2128284
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
NMR: suitable
gas chromatography (GC): suitable

mp

124-127 °C

suitability

passes test for identity (NMR)

application(s)

agriculture
environmental

format

neat

SMILES string

COc1ccc(NC(=O)N(C)C)cc1Cl

InChI

1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14)

InChI key

DSRNRYQBBJQVCW-UHFFFAOYSA-N

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General description

Metoxuron is a phenylurea herbicide widely used for agricultural applications.

Application

Metoxuron may be used as an analytical reference standard for the determination of the analyte in soil, aqueous samples, crops and vegetables by various chromatographic techniques.
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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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[Effect of dosanex on the immunologic reactions in animals].
M V Tat'ian et al.
Gigiena i sanitariia, (2)(2), 85-86 (1983-02-01)
Francisco A Macías et al.
Journal of agricultural and food chemistry, 54(4), 1040-1048 (2006-02-16)
Avena fatua L. (wild oat) and Lolium rigidum Gaud. (rigid ryegrass) are highly problematic weeds affecting a wide variety of cereal crops worldwide. The fact that both of these weeds have developed resistance to several herbicide groups made them optimal
W Sanchez et al.
Marine environmental research, 62 Suppl, S29-S33 (2006-05-19)
This study examined the response of 7-ethoxyresorufine-O-deethylase, glutathione-S-transferase, glutathione peroxidase, glutathione content, level of thiobarbituric acid reactive compounds and circulating vitellogenin, in three-spined sticklebacks after 21 days of exposure to Diquat herbicide, commercial nonylphenol polyethoxylate adjuvant and mixture between Diquat
Determination of pesticides in vegetables using large-volume injection column liquid chromatography--electrospray tandem mass spectrometry.
Hogenboom AC, et al.
Journal of Chromatography A, 892(1-2), 379-390 (2000)
Aqueous oxidation of phenylurea herbicides by triplet aromatic ketones.
Canonica S, et al.
Environmental Science & Technology, 40(21), 6636-6641 (2006)

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