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Bromacil

PESTANAL®, analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C9H13BrN2O2
Numéro CAS:
Poids moléculaire :
261.12
Numéro Beilstein :
6804755
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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)

Clé InChI

CTSLUCNDVMMDHG-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Informations légales

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

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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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