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D2425

Sigma-Aldrich

Diuron

≥98%

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
Beilstein:
2215168
EC Number:
206-354-4
MDL number:
MFCD00018136
UNSPSC Code:
12352100
PubChem Substance ID:
57654085
NACRES:
NA.22

Assay

≥98%

form

powder

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

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Related Categories

Application

  • The Fabrication and Property Characterization of a Ho(2)YSbO(7)/Bi(2)MoO(6) Heterojunction Photocatalyst and the Application of the Photodegradation of Diuron under Visible Light Irradiation.: This research investigates a novel photocatalyst′s ability to degrade diuron under visible light, offering insights into sustainable environmental remediation technologies (Hao and Luan, 2024).

Signal Word

Warning

Hazard Statements

H302,H351,H373,H410

Hazard Classifications

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

Target Organs

Blood

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Michael Jahn et al.
Cell reports, 25(2), 478-486 (2018-10-12)
Cyanobacteria must balance separate demands for energy generation, carbon assimilation, and biomass synthesis. We used shotgun proteomics to investigate proteome allocation strategies in the model cyanobacterium Synechocystis sp. PCC 6803 as it adapted to light and inorganic carbon (Ci) limitation.
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
Bernard Lepetit et al.
Plant physiology, 161(2), 853-865 (2012-12-05)
In diatoms, the process of energy-dependent chlorophyll fluorescence quenching (qE) has an important role in photoprotection. Three components are essential for qE: (1) the light-dependent generation of a transthylakoidal proton gradient; (2) the deepoxidation of the xanthophyll diadinoxanthin (Dd) into
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
Perry J Mitchell et al.
Environmental science & technology, 47(1), 412-419 (2012-12-05)
Reported correlations between organic contaminant sorption affinity and soil organic matter (OM) structure vary widely, suggesting the importance of OM physical conformation and accessibility. Batch equilibration experiments were used to examine the sorption affinity of bisphenol A, atrazine, and diuron
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