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Merck

45350

Supelco

Bromacil

PESTANAL®, analytical standard

Synonym(e):

Isocil

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About This Item

Empirische Formel (Hill-System):
C9H13BrN2O2
CAS-Nummer:
Molekulargewicht:
261.12
Beilstein:
6804755
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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)

InChIKey

CTSLUCNDVMMDHG-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Analysenzertifikate (COA)

Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

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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