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Diuron-d6

PESTANAL®, analytical standard

Synonym(s):

3-(3,4-Dichlorophenyl)-1,1-dimethylurea-d6

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About This Item

Empirical Formula (Hill Notation):
C9H4D6Cl2N2O
CAS Number:
Molecular Weight:
239.13
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

mass shift

M+6

SMILES string

[2H]C([2H])([2H])N(C(=O)Nc1ccc(Cl)c(Cl)c1)C([2H])([2H])[2H]

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)/i1D3,2D3

InChI key

XMTQQYYKAHVGBJ-WFGJKAKNSA-N

General description

Diuron-d6 is an isotopically labeled analog of the phenylurea herbicide diuron, which is used for the control of annual grass and broad-leaved weeds in agriculture.

Application

Diuron-d6 may be used as an internal standard for the quantification of diuron in:
  • Sewage sludge using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS).
  • Water samples using stir bar sorptive extraction and liquid desorption coupled to liquid chromatography-tandem mass spectrometry (SBSE-LD-LC-MSMS).

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

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Description
Pricing

Signal Word

Warning

Hazard Statements

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

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Certificates of Analysis (COA)

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Multiresidue analysis of atrazine, diuron and their degradation products in sewage sludge by liquid chromatography tandem mass spectrometry.
Ghanem A, et al.
Analytical and Bioanalytical Chemistry, 391(1), 345-352 (2008)
Augusto A Vieira et al.
Food chemistry, 242, 475-480 (2017-10-19)
Booster biocides have been widely applied to ships and other submerged structures. These compounds can be released into the marine environment as the result of vessel hull leaching and may remain in different environmental compartments. This study aimed at introducing
Stir bar sorptive extraction coupled to liquid chromatography-tandem mass spectrometry for the determination of pesticides in water samples: Method validation and measurement uncertainty.
Margoum C, et al.
Talanta, 116(1), 1-7 (2013)
N-nitrosodimethylamine Formation During Chlorination of Diuron with Influence Analysis of the Sacramento-San Joaquin Delta Water Quality for Urban Uses (2009)
Kerstin Schäfer et al.
Current biology : CB, 30(5), 840-853 (2020-02-23)
Twin arginine translocation (TAT) pathways have been extensively studied in bacteria and chloroplasts for their role in membrane translocation of folded proteins. However, an increasing number of organisms have been found to contain mitochondria-located TAT subunits, including plant mitochondria, which

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