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关于此项目
经验公式(希尔记法):
C9H13BrN2O2
化学文摘社编号:
分子量:
261.12
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
206-245-1
Beilstein/REAXYS Number:
6804755
MDL number:
产品名称
除草定, PESTANAL®, analytical standard
InChI key
CTSLUCNDVMMDHG-UHFFFAOYSA-N
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)
SMILES string
CCC(C)N1C(=O)NC(C)=C(Br)C1=O
grade
analytical standard
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
Quality Level
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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.
General description
Bromacil is an active ingredient of the commercially marketed pesticide, Krovar, widely used for weed control in citrus orchards.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
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)
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)
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')
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
S V Babitskaia et al.
Prikladnaia biokhimiia i mikrobiologiia, 40(4), 414-420 (2004-10-01)
Two new derivatives of phosphatidylcholine with intramolecular fluorescence quenching were obtained by substituting residues of pyrene butyric and bromine-containing fatty acids for acyl chains. The two compounds can be used for quantitative evaluation of catalytic activity of pancreatic phospholipase A2
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