36162
莠谷隆
PESTANAL®, analytical standard
别名:
N′-(4-溴苯基)-N-甲氧基-N-甲脲
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关于此项目
经验公式（希尔记法）:
C9H11BrN2O2
化学文摘社编号:
分子量:
259.10
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
221-301-5
Beilstein/REAXYS Number:
2103964
MDL number:
InChI key
WLFDQEVORAMCIM-UHFFFAOYSA-N
InChI
1S/C9H11BrN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)
SMILES string
CON(C)C(=O)Nc1ccc(Br)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
application(s)
agriculture
environmental
format
neat
Quality Level
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General description
Metobromuron is a phenylurea herbicide widely used in pre- and post-emergence control of blackgrass, silky bentgrass, wild oats and annual meadow grass.
Application
Metobromuron may be used as an analytical reference standard for the quantification of the analyte in vegetables, soil, tobacco and aqueous samples by various chromatography 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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
Method development for the determination of selected pesticides on tobacco by high-performance liquid chromatography--electrospray ionisation-tandem mass spectrometry.
Mayer-Helm B, et al.
Talanta, 74(5), 1184-1190 (2008)
Application of solid-phase microextraction for determining phenylurea herbicides and their homologous anilines from vegetables.
Berrada H, et al.
Journal of Chromatography A, 1042(1-2), 9-14 (2004)
The determination of some substituted urea herbicide residues in soil by electron-capture gas chromatography.
McKone CE
Journal of Chromatography A, 44(1-2), 60-66 (1969)
Photochemical versus coupled photochemical--biological flow system for the treatment of two biorecalcitrant herbicides: metobromuron and isoproturon.
Parra S, et al.
Applied Catalysis. B, Environmental, 27(3), 153-168 (2000)
Vincent J Smith et al.
Carbohydrate research, 344(17), 2388-2393 (2009-10-06)
We report the formation of inclusion complexes between the phenylurea herbicide metobromuron [3-(p-bromophenyl)-1-methoxy-1-methylurea] and beta- and gamma-cyclodextrin in the solid state. Formation of crystalline inclusion complexes by the kneading method was confirmed by powder X-ray diffraction and further structural characterization
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