36174
灭草隆
PESTANAL®, analytical standard
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关于此项目
线性分子式:
ClC6H4NHCON(CH3)2
化学文摘社编号:
分子量:
198.65
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-766-1
Beilstein/REAXYS Number:
2097922
MDL number:
InChI key
BMLIZLVNXIYGCK-UHFFFAOYSA-N
InChI
1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)
SMILES string
CN(C)C(=O)Nc1ccc(Cl)cc1
grade
analytical standard
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
Quality Level
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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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
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)
Hana Mest'ánková et al.
Chemosphere, 57(10), 1307-1315 (2004-11-03)
The degradation of Monuron (3-(4-chlorophenyl)-1,1-dimethylurea) photoinduced by Fe(III) in aqueous solution has been investigated. The rate of degradation depends on the concentration of Fe(OH)2+, the most photoreactive species in terms of *OH radical formation. These *OH radicals are able to
W Chu et al.
Chemosphere, 86(11), 1079-1086 (2011-12-30)
A comprehensive study of the degradation of monuron, one of the phenylurea herbicides, was conducted by UV-Vis/WO(3) process. It was found that hydroxyl radicals played a major role in the decay of monuron while other radicals (e.g. superoxide) and hole
L C Rai et al.
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 5(1), 13-16 (1992-01-01)
The impact of 2,4-dinitrophenol and chlorophenyl dimethylurea on ATP content, carbon fixation, O2 evolution, nitrogenase activity and Cr uptake of Anabaena doliolum has been studied. 2,4-Dinitrophenol has been found to be more toxic than chlorophenyldimethylurea for all these processes. However
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
实验方案
-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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