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Merck

45463

Diuron

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C9H10Cl2N2O
CAS Number:
330-54-1
Molecular Weight:
233.09
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756756
EC Number:
206-354-4
Beilstein/REAXYS Number:
2215168
MDL number:
MFCD00018136

Key Documents

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Product Name

Diuron, PESTANAL®, analytical standard

InChI key

XMTQQYYKAHVGBJ-UHFFFAOYSA-N

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)

SMILES string

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

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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

100

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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

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN0071
BCCJ0691
BCCF0588
BCBZ5361
BCBS1743

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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
Ezequiel Petrillo et al.
Science (New York, N.Y.), 344(6182), 427-430 (2014-04-26)
Light is a source of energy and also a regulator of plant physiological adaptations. We show here that light/dark conditions affect alternative splicing of a subset of Arabidopsis genes preferentially encoding proteins involved in RNA processing. The effect requires functional
Priyanka Sharma et al.
Biosensors & bioelectronics, 39(1), 99-105 (2012-08-14)
We report a novel in-situ electrochemical synthesis approach for the formation of functionalized graphene-graphene oxide (fG-GO) nanocomposite on screen-printed electrodes (SPE). Electrochemically controlled nanocomposite film formation was studied by transmission electron microscopy (TEM) and Raman spectroscopy. Further insight into the
Robert Musiol et al.
Bioorganic & medicinal chemistry, 15(3), 1280-1288 (2006-12-05)
The lack of the wide spectrum of biological data is an important obstacle preventing the efficient molecular design. Quinoline derivatives are known to exhibit a variety of biological effects. In the current publication, we tested a series of novel quinoline
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
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