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D2425

Sigma-Aldrich

Diuron

≥98%

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Synonym(s):
3-(3,4-Dichlorophenyl)-1,1-dimethylurea
Empirical Formula (Hill Notation):
C9H10Cl2N2O
CAS Number:
Molecular Weight:
233.09
Beilstein:
2215168
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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1 of 4

This Item
169021545040410
Diuron ≥98%

Sigma-Aldrich

D2425

Diuron

Diuron certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

16902

Diuron

N,N′-Dimethylurea (sym.), ≥99% (from N)

Sigma-Aldrich

15450

N,N′-Dimethylurea

N,N′-Dimethylurea (sym.), ≥95.0% (HPLC), technical

Sigma-Aldrich

40410

N,N′-Dimethylurea

form

powder

form

-

form

solid

form

-

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

200

Gene Information

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

Gene Information

-

Gene Information

-

Gene Information

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Blood

Storage Class Code

13 - Non 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

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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
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
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

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