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Supelco

Bromacil

PESTANAL®, analytical standard

Synonym(s):

5-Bromo-3-sec.-butyl-6-methyluracil

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About This Item

Empirical Formula (Hill Notation):
C9H13BrN2O2
CAS Number:
Molecular Weight:
261.12
Beilstein:
6804755
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

CCC(C)N1C(=O)NC(C)=C(Br)C1=O

InChI

1S/C9H13BrN2O2/c1-4-5(2)12-8(13)7(10)6(3)11-9(12)14/h5H,4H2,1-3H3,(H,11,14)

InChI key

CTSLUCNDVMMDHG-UHFFFAOYSA-N

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General description

Bromacil is an active ingredient of the commercially marketed pesticide, Krovar, widely used for weed control in citrus orchards.

Application

Bromacil may be used as an analytical reference standard for the quantification of the analyte in environmental samples using different chromatography techniques.
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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

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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An enzyme immunoassay for the environmental monitoring of the herbicide bromacil
Bekheit.MKH, et al.
Journal of Agricultural and Food Chemistry, 41(11), 2220-2227 (1993)
Erol Ayranci et al.
Journal of hazardous materials, 112(1-2), 163-168 (2004-07-01)
The removal of pesticides such as metribuzin, bromacil, 2,4-d and atrazine from aqueous solutions was studied by adsorption on high area carbon cloth. The adsorption process was followed by in situ UV-spectrophotometric technique in a specially designed adsorption cell. Spectroscopic
Cliff R Seery et al.
Environmental pollution (Barking, Essex : 1987), 140(1), 43-51 (2005-09-07)
The innovative bioassay described here involves chlorophyll a fluorescence measurements of gametes from the macroalgae, Hormosira banksii, where gametes (eggs) were exposed to Diuron, Irgarol and Bromacil. Response was assessed as percent inhibition from control of effective quantum yield (DeltaF/Fm')
Direct determination of bromacil and diuron residues in environmental water samples by coupled-column liquid chromatography and large-volume injection
Sancho.V.J, et al.
Journal of Chromatography A, 761(1-2), 322-326 (1997)
Song-Bae Kim et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 42(5), 529-537 (2007-06-15)
This study was conducted to determine the significance of bromacil transport as a function of water and carbon content in soils and to explore the implications of neglecting sorption when making assessments of travel time of bromacil through the vadose

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