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Key Documents

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45494

Supelco

Fenuron

PESTANAL®, analytical standard

Sinónimos:

1,1-Dimethyl-3-phenylurea

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About This Item

Fórmula empírica (notación de Hill):
C9H12N2O
Número de CAS:
101-42-8
Peso molecular:
164.20
Beilstein/REAXYS Number:
2208535
EC Number:
202-941-4
MDL number:
MFCD00025662
UNSPSC Code:
41116107
PubChem Substance ID:
329756786
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

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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Certificados de análisis (COA)

Lot/Batch Number
BCCD9984
BCBX4374
SZBD238XV
SZBA218XV
SZE6009X

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C Richard et al.
Environmental science & technology, 38(7), 2052-2057 (2004-04-29)
The IHSS soil humic acid (HA) standard and two HAs from soils of very different origin (Chernozem and Ranker) were fractionated by tandem size-exclusion chromatography-polyacrylamide gel electrophoresis. From each HA, three fractions with different molecular sizes (MSs) and electrophoretic mobilities
[Embryotropic effect of fenuron].
L T Voloshina
Vrachebnoe delo, (2)(2), 103-105 (1985-02-01)
Yen Hai Dao et al.
Water research, 45(11), 3309-3317 (2011-04-26)
The relative rates of degradation of three hydroxyl radical probe compounds (atrazine, fenuron and parachlorobenzoic acid (pCBA)) by Fe(III)/H(2)O(2) (pH = 2.85), Fe(III)NTA/H(2)O(2) (neutral pH), Fe(II)/O(2), Fe(II)NTA/O(2), Fe(II)/H(2)O(2) and Fe(II)NTA/H(2)O(2) (neutral pH) have been investigated using the competitive kinetic method.
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)
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