31102
2,6-Dichlorophenol
PESTANAL®, analytical standard
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About This Item
Fórmula lineal:
Cl2C6H3OH
Número de CAS:
Peso molecular:
163.00
Beilstein/REAXYS Number:
1447806
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Productos recomendados
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
bp
218-220 °C (lit.)
mp
64-66 °C (lit.)
application(s)
agriculture
environmental
format
neat
SMILES string
Oc1c(Cl)cccc1Cl
InChI
1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H
InChI key
HOLHYSJJBXSLMV-UHFFFAOYSA-N
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Categorías relacionadas
General description
2,6-Dichlorophenol is an organochloride of phenol and also a degradation product of some pesticides.Chloride phenols are widely used by the chemical industry as an intermediate product in synthesis and previously were frequently applied as wood preservatives and fungicides. They are considered one of the emerging pollutants in wastewater due to their extreme corrosive nature and toxicity even at low concentrations.
Application
2,6-Dichlorophenol may have the following uses:
- To study the kinetics, performance, and mechanism of the oxidative degradation of 2,6-dichlorophenol (2,6-DCP) by ferrate (VI) (Fe(VI))
- Removal of 2,6-dichlorophenol in water by copper oxide (CuO) activated peroxymonosulfate as catalyst
- Removal of 2,6-dichlorophenol by adsorption with activated polypropylene nanofiber
- Degradation of 2,6-dichlorophenol by Fe-doped titanium oxide(TiO2) sonophotocatalytic process
- Determination of 2,6-dichlorophenol by surface-enhanced Raman scattering (SERS) with molecular imprinting
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Yu Tian et al.
Water research, 47(1), 279-288 (2012-11-06)
Distribution variation of a metabolic uncoupler, 2,6-dichlorophenol (2,6-DCP), in long-term sludge culture was studied, and the effects on sludge reduction and biological inhibition of this chemical during the 90-day operation were established. The extracellular polymeric substance (EPS) matrix functioned as
Anna Maria Polcaro et al.
Journal of hazardous materials, 148(3), 505-512 (2007-04-07)
This paper presents the results of a study on the electrokinetic treatment of kaolinite and humic acid kaolinite complexes spiked with 2,6-dichlorophenol or 3-(3,4-dichlorophenyl)-1,1-dimethylurea (diuron). In particular, the attention was paid to the interaction between solid surface and dissolved organics:
Ulker Beker et al.
Environmental geochemistry and health, 32(4), 291-296 (2010-04-14)
The objective of this study is to examine the adsorption-desorption behavior of a magnetically active hybrid sorbent (MAHS) material, prepared by dispersing colloid-like hydrated iron oxide particles in the outer periphery of a macroporous ion-exchange resin (Amberlite XAD-2). The experimental
Kennedy Kiriira Gachoka et al.
Revista brasileira de parasitologia veterinaria = Brazilian journal of veterinary parasitology : Orgao Oficial do Colegio Brasileiro de Parasitologia Veterinaria, 20(4), 347-350 (2011-12-15)
In order to clarify the role of 2,6-dichlorophenol (2,6-DCP) in the courtship of Amblyomma cajennense, sexually mature males that had previously fed on rabbits were tested in bioassays. The males were released onto dummies treated with whole female extract or
B Karthikeyan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(3), 619-623 (2005-07-19)
Raman spectra of phenoxyacetic acid and chlorine substituted phenoxyacetic acids viz., o-chlorophenoxyacetic acid, p-chlorophenoxyacetic acid and 2,6-dichlorophenoxyacetic acid have been analysed with the aid of abinitio theoretical calculations. The effect of chlorine substituents on the Raman spectra of phenoxyacetic acid
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