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45377

Supelco

Chlorobromouron

PESTANAL®, analytical standard

Synonym(s):

Chlorbromuron

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About This Item

Empirical Formula (Hill Notation):
C9H10BrClN2O2
CAS Number:
13360-45-7
Molecular Weight:
293.54
Beilstein:
2128736
EC Number:
236-411-9
MDL number:
MFCD00055474
UNSPSC Code:
41116107
PubChem Substance ID:
329756684
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

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

InChI

1S/C9H10BrClN2O2/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

NLYNUTMZTCLNOO-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

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H332,H411

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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)

Lot/Batch Number
BCCJ8231
BCBX9935
SZBD273XV
SZB8268XV
SZE8268X

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J Clemy Monicka et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 94, 30-35 (2012-04-21)
FT-Raman and IR spectra of the herbicidal compound chlorbromuron have been recorded and analyzed. The detailed interpretation of the vibrational spectra has been carried out with the aid of normal coordinate analysis (NCA) following the scaled quantum mechanical force field
Susana Silva Martínez et al.
Water research, 43(1), 33-40 (2008-11-07)
The removal of low concentration of chlorbromuron herbicide in aqueous systems was carried out by electro-Fenton process comprised of three-electrode divided and undivided cell with a reticulated vitreous carbon cathode and platinum anode. The electro-Fenton was also carried out in
[Comparative gonadotoxic effect of maloran in laboratory animals after its administration by different routes].
N R Shepel'skaia et al.
Gigiena i sanitariia, (3)(3), 84-85 (1985-03-01)
[Hygienic standardization of the herbicide Maloran in the air of a work area].
G A Voĭtenko et al.
Gigiena i sanitariia, (8)(8), 76-78 (1981-08-01)
Liying Guo et al.
Mikrochimica acta, 186(7), 464-464 (2019-06-24)
Graphene oxide was covalently modified with p-phenylenediamine via a diazonium reaction. The resulting material was employed as a sorbent for the solid-phase extraction of six phenylurea herbicides (metoxuron, monuron, chlortoluron, isoproturon, monolinuron, and buturon) from environmental water and lettuce leafs.
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