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36174

Supelco

Monuron

PESTANAL®, analytical standard

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About This Item

Linear Formula:
ClC6H4NHCON(CH3)2
CAS Number:
150-68-5
Molecular Weight:
198.65
Beilstein:
2097922
EC Number:
205-766-1
MDL number:
MFCD00018556
UNSPSC Code:
41116107
PubChem Substance ID:
329755318
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

173-174 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

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

InChI

1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)

InChI key

BMLIZLVNXIYGCK-UHFFFAOYSA-N

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General description

Monuron belongs to the arylurea family of herbicides, which is widely used in agriculture.

Application

Monuron may be used as a reference standard in the determination of monuron in rice and corn using high performance liquid chromatography coupled with fluorescence detection combined with ultraviolet decomposition and post-column derivatization.
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

Warning

Hazard Statements

H302,H351,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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)

Lot/Batch Number
BCCJ1502
BCBW5539

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A highly sensitive and rapid ELISA for the arylurea herbicides diuron, monuron, and linuron.
Schneider P, et al.
Journal of Agricultural and Food Chemistry, 42(2), 413-422 (1994)
[Hygienic regulation of the monurone content of soil].
Iu N Talakin et al.
Gigiena i sanitariia, (12)(12), 55-57 (1984-12-01)
W Chu et al.
Chemosphere, 69(2), 177-183 (2007-06-23)
Photodegradation of the phenylurea herbicide monuron by using riboflavin (Rf), a sensitizer, was investigated by varying the doses of monuron and Rf in this work. An enhanced photochemical effect was observed in the process compared with the direct photolysis by
Hadjira Boucheloukh et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(8), 1339-1345 (2012-06-05)
The photo-induced transformation of monuron (3-(4-chlorophenyl)-1,1 dimethylurea) was investigated in an aqueous solution containing nitrates and nitrites at 310 nm and 365 nm, respectively. In both NO(3)(-) and NO(2)(-) conditions, the degradation of monuron followed pseudo-first order kinetics. The intermediate
W Chu et al.
Journal of agricultural and food chemistry, 55(14), 5708-5713 (2007-06-15)
The immobilization of cobalt ion on different media to catalyze oxone has been investigated. A probe herbicide, Monuron, was effectively degraded by using Co2+/oxone systems. For Co2+ supported on zeolite, 100% of Monuron could be removed within a 10 min
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Protocols

US EPA Method 632: HPLC Analysis of Pesticides on Ascentis® C18

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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