36605
2,6-二氯苯甲酰胺
PESTANAL®, analytical standard
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关于此项目
线性分子式:
Cl2C6H3CONH2
化学文摘社编号:
分子量:
190.03
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-918-4
Beilstein/REAXYS Number:
1869103
MDL number:
InChI key
JHSPCUHPSIUQRB-UHFFFAOYSA-N
InChI
1S/C7H5Cl2NO/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H2,10,11)
SMILES string
NC(=O)c1c(Cl)cccc1Cl
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
196-199 °C (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
General description
2,6-Dichlorobenzamide is found to be a degradation product and metabolite of the pesticide dichlobenil.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Basil Uthuppu et al.
Analytica chimica acta, 748, 95-103 (2012-10-02)
Dichlobenil is an extensively used herbicide worldwide which is transformed to the mobile 2,6-dichlorobenzamide (BAM) in soil. BAM has been found in many European groundwater resources that are exploited for drinking water. Currently, immunoassay based monitoring technique (plate based ELISA)
Ole R Sjøholm et al.
Environmental pollution (Barking, Essex : 1987), 158(12), 3618-3625 (2010-09-11)
Mineralisation capability was studied in the 2,6-dichlorobenzamide (BAM)-degrading Aminobacter sp. MSH1 under growth-arrested conditions. Cells were starved in mineral salts (MS) solution or groundwater before (14)C-labelled BAM (0.1mM) was added. Cell physiology was monitored with a panel of vitality stains combined
Erik Belleville et al.
BioTechniques, 35(5), 1044-1051 (2003-11-25)
Analytical protein microarrays offering highly parallel analysis can become an invaluable tool for a wide range of immunodiagnostic applications. Here we describe factors that influence the sensitivity of a competitive immunomicroarray that quantifies small molecules; in this case, the pesticides
Gitte Gotholdt Jensen et al.
Journal of chromatography. A, 1216(27), 5199-5206 (2009-06-03)
An analytical method was developed for the determination of 2,6-dichlorobenzamide (BAM) and five degradation products thereof including 2-chlorobenzamide (OBAM), 2,6-dichlorobenzoic acid (DCBA), 2-chlorobenzoic acid (OBA), benzoic acid (BA) and benzamide (BAD) in water samples. Solid-phase extraction was combined with liquid
Efficient biodegradation of dihalogenated benzonitrile herbicides by recombinant Escherichia coli harboring nitrile hydratase-amidase pathway
Pei X, et al.
Biochemical Engineering Journal (2017)
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