31102
2,6-Dichlorophenol
PESTANAL®, analytical standard
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About This Item
Linear Formula:
Cl2C6H3OH
CAS Number:
Molecular Weight:
163.00
Beilstein:
1447806
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
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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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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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S Almeda et al.
Analytica chimica acta, 587(1), 97-103 (2007-03-28)
Actually there is a great trend on the development of effective analytical methods for monitoring trace levels of various phenols which can indicate, among others compounds, the water quality. A simple, inexpensive supported liquid membrane (SLM) device was used in
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
Qiang He et al.
Applied microbiology and biotechnology, 65(4), 377-382 (2004-06-05)
A continuous fed-batch reactor system was developed to rapidly obtain dense chlororespiring cultures of Anaeromyxobacter dehalogenans strain 2CP-C. A syringe pump continuously delivered concentrated 2,6-dichlorophenol (50-150 mM) to an anaerobic reactor vessel at a rate that sustained linear growth but
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
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
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