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Documenti

45350

Supelco

Bromacil

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C9H13BrN2O2
Numero CAS:
Peso molecolare:
261.12
Beilstein:
6804755
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
environmental

Formato

neat

Stringa SMILE

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)
CTSLUCNDVMMDHG-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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

Applicazioni

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.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation markEnvironment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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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