Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

45494

Supelco

Fenuron

PESTANAL®, analytical standard

Synonym(s):

1,1-Dimethyl-3-phenylurea, Fenuron

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C9H12N2O
CAS Number:
101-42-8
Molecular Weight:
164.20
Beilstein:
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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCD9984
BCBX4374

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

[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)
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)
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
[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)
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
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service