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Supelco

Monuron

PESTANAL®, analytical standard

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About This Item

Fórmula linear:
ClC6H4NHCON(CH3)2
Número CAS:
150-68-5
Peso molecular:
198.65
Beilstein:
2097922
Número CE:
205-766-1
Número MDL:
MFCD00018556
Código UNSPSC:
41116107
ID de substância PubChem:
329755318
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pf

173-174 °C (lit.)

aplicação(ões)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

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)

chave InChI

BMLIZLVNXIYGCK-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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.

Informações legais

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

Palavra indicadora

Warning

Frases de perigo

H302,H351,H410

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCJ1502
BCBW5539
SZBD119XV
SZBD114XV
SZB8114XV

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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)
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
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
[Hygienic regulation of the monurone content of soil].
Iu N Talakin et al.
Gigiena i sanitariia, (12)(12), 55-57 (1984-12-01)
Maria Bobu et al.
Chemosphere, 63(10), 1718-1727 (2005-11-18)
The photodegradation of monuron (3-(4-chlorophenyl)-1,1-dimethylurea) in aqueous solutions under simulated solar irradiation has been conducted by different advanced oxidation processes (UV/H(2)O(2), UV/H(2)O(2)/Fe(2+), UV/H(2)O(2)/TiO(2), UV/TiO(2), dark H(2)O(2)/Fe(3+)). The degradation rates were always higher for the homogeneous catalysis in photo-Fenton reactions (UV/H(2)O(2)/Fe(2+))
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Protocolos

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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