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Key Documents

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45463

Supelco

Diuron

PESTANAL®, analytical standard

Sinónimos:

3-(3,4-Dichlorophenyl)-1,1-dimethylurea

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About This Item

Fórmula empírica (notación de Hill):
C9H10Cl2N2O
Número de CAS:
330-54-1
Peso molecular:
233.09
Beilstein/REAXYS Number:
2215168
EC Number:
206-354-4
MDL number:
MFCD00018136
UNSPSC Code:
41116107
PubChem Substance ID:
329756756
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

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1

InChI

1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)

InChI key

XMTQQYYKAHVGBJ-UHFFFAOYSA-N

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Categorías relacionadas

Application

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

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT RE 2 Inhalation

target_organs

Blood

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ0691
BCCF0588
BCBZ5361
BCBS1743
BCBS0837V

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S Giacomazzi et al.
Chemosphere, 56(11), 1021-1032 (2004-07-28)
Diuron is a biologically active pollutant present in soil, water and sediments. A synthesis of literature data on its physicochemical properties, partitioning behaviour, abiotic and biotic transformations, toxicological and ecotoxicological impacts has been here performed. Data have shown that diuron
Sheridan M Martin et al.
Journal of hazardous materials, 231-232, 70-78 (2012-07-17)
We studied the sorption-desorption behaviour of two herbicides (diuron and artrazine) in a soil rich in Fe and Al oxides (Ferrosol), either amended freshly with two different types of biochars or that contained biochars aged under field conditions. Standard batch
Robert Musiol et al.
Bioorganic & medicinal chemistry, 16(8), 4490-4499 (2008-03-18)
Two series of amides based on quinoline scaffold were designed and synthesized in search of photosynthesis inhibitors. The compounds were tested for their photosynthesis-inhibiting activity against Spinacia oleracea L. and Chlorella vulgaris Beij. The compounds lipophilicity was determined by the
Lijin Tian et al.
Physical chemistry chemical physics : PCCP, 15(9), 3146-3154 (2013-01-24)
Photosystems I (PSI) and II (PSII) are two major pigment-protein complexes of photosynthetic organisms that function in series to convert sunlight energy into chemical energy. We have studied the picosecond fluorescence behaviour of the core of both photosystems in vivo
Tobias Wunder et al.
Planta, 237(2), 541-558 (2012-10-23)
Reversible phosphorylation of LHCII, the light-harvesting complex of photosystem II, controls its migration between the two photosystems (state transitions), and serves to adapt the photosynthetic machinery of plants and green algae to short-term changes in ambient light conditions. The thylakoid
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Protocolos

HPLC Analysis of Atrazine Herbicides on Ascentis® Express C18

Separation of Atrazine-desethyl; Metoxuron; Hexazinone; Simazine; Cyanazine; Methabenzthiazuron; Atrazine; Monolinuron; Diuron; Isoproturon; Metobromuron; Metazachlor; Sebuthylazin; Linuron; Metolachlor

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