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36141

Supelco

Linuron

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H10Cl2N2O2
CAS Number:
Molecular Weight:
249.09
Beilstein:
2128725
EC Number:
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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

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

InChI

1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)

InChI key

XKJMBINCVNINCA-UHFFFAOYSA-N

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General description

Linuron is a substituted phenyl urea herbicide used for controlling weeds in carrot plantations.

Application

Linuron has been used as a standard for the determination of linuron in water and agricultural preparations by HPLC method using stripping voltammetry with carbon paste electrode.
Linuron may be used as a reference standard in the determination of linuron in fruits using high-performance liquid chromatography (HPLC).
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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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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Effect of Linuron (3- (3, 4-dichlorophenyl) -1- Methoxy -1- Methylurea) on Carrot Varieties
McLaughlin FM
Toxicology and Applied Pharmacology, 119(2), 195-204 (1972)
The determination of the herbicide linuron in Saskatoon berries using HPLC with column switching
Cessna, Allan J
Journal of Liquid Chromatography, 11(3), 725-735 (1988)
Investigation of a mechanism for Leydig cell tumorigenesis by linuron in rats
Cook, et al.
Toxicology and Applied Pharmacology, 119(2), 195-204 (1993)
Kristel Sniegowski et al.
Applied and environmental microbiology, 77(18), 6614-6621 (2011-08-02)
On-farm biopurification systems (BPS) treat pesticide-contaminated wastewater of farms through biodegradation. Adding pesticide-primed soil has been shown to be beneficial for the establishment of pesticide-degrading populations in BPS. However, no data exist on the response of pesticide-degrading microbiota, either endogenous
Kristel Sniegowski et al.
Chemosphere, 88(9), 1114-1118 (2012-06-12)
Addition of pesticide-primed soil containing adapted pesticide degrading bacteria to the biofilter matrix of on farm biopurification systems (BPS) which treat pesticide contaminated wastewater, has been recommended, in order to ensure rapid establishment of a pesticide degrading microbial community in

Protocols

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

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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