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45494

Supelco

Fenuron

PESTANAL®, analytical standard

Synonym(s):

1,1-Dimethyl-3-phenylurea, Fenuron

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About This Item

Empirical Formula (Hill Notation):
C9H12N2O
CAS Number:
Molecular Weight:
164.20
Beilstein/REAXYS Number:
2208535
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
environmental

format

neat

SMILES string

CN(C)C(=O)Nc1ccccc1

InChI

1S/C9H12N2O/c1-11(2)9(12)10-8-6-4-3-5-7-8/h3-7H,1-2H3,(H,10,12)

InChI key

XXOYNJXVWVNOOJ-UHFFFAOYSA-N

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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

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pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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H H Attaway et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 17(6), 683-699 (1982-01-01)
Anaerobic degradation of diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea], monuron [3-(4-chlorophenyl)-1,1-dimethylurea], and fenuron [1,1-dimethyl-3-phenylurea] were studied. Herbicide containing media (reduced with cysteine-HCl and under 95% N2:5% CO2 gas phase) were inoculated with pond sediments. Sediment from a diuron-treated pond dehalongenated diuron to 3-(3-chlorophenyl)-1,1-dimethylurea (CPDU)
[Hygienic evaluation of the method of ozonization used for detoxication of aqueous solutions of urea derivatives].
V I Tsipriian et al.
Gigiena i sanitariia, (2)(2), 83-85 (1985-02-01)
[Hygienic significance of pathomorphologic changes of the organs in albino rats in studying the embryotoxic effect of fenuron].
Iu N Talakin et al.
Gigiena i sanitariia, (9)(9), 73-75 (1989-09-01)
J P Aguer et al.
Chemosphere, 44(2), 205-209 (2001-07-11)
Humic acids (HAs) from three soils of different origin (Chernozem, Ferralsol and Ranker) have been fractionated by coupling size exclusion chromatography (SEC) and polyacrylamide gel electrophoresis (PAGE) on three fractions (fractions A, B, C + D) with different molecular sizes
Humic substances as natural photoinducers degrading pesticides in the environment.
O E Trubetskaya et al.
Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections, 406, 94-96 (2006-04-01)

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