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Merck
CN

31102

2,6-Dichlorophenol

PESTANAL®, analytical standard

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About This Item

Linear Formula:
Cl2C6H3OH
CAS Number:
87-65-0
Molecular Weight:
163.00
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753647
EC Number:
201-761-3
Beilstein/REAXYS Number:
1447806
MDL number:
MFCD00002176

Key Documents

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Product Name

2,6-Dichlorophenol, PESTANAL®, analytical standard

InChI key

HOLHYSJJBXSLMV-UHFFFAOYSA-N

InChI

1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H

SMILES string

Oc1c(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

bp

218-220 °C (lit.)

mp

64-66 °C (lit.)

application(s)

agriculture
environmental

format

neat

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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

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.

Legal Information

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

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

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

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8154
BCCC4286

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Enzo Laurenti et al.
Journal of inorganic biochemistry, 92(1), 75-81 (2002-09-17)
The reaction mechanism of the oxidation of 2,6-dichlorophenol (2,6-DCP) by horseradish peroxidase (HRP) and H2O2 has been investigated and the reaction products have been characterized by UV-visible and mass spectrometry. Evidence for the dimerization of 2,6-DCP to 3,3',5,5'-tetrachloro-4,4'-dihydroxybiphenyl and the
A M Polcaro et al.
Annali di chimica, 91(3-4), 203-210 (2001-05-31)
The paper examines the effect of chloride on the oxidation of 2,6-dichlorophenol (DCP) performed at TiO2/RuO2 DSA anodes, which are specific catalysts for chlorine evolution. The results indicate that chlorine/hypochlorite originating from chloride oxidation in certain favourable conditions reacts with
Lígia M F Borges et al.
Experimental & applied acarology, 27(3), 223-230 (2003-02-21)
The objective of this study was to evaluate the role of 2,6-dichlorophenol (2,6-DCP) as sex pheromone of Anocentor nitens. Sex pheromones were extracted by submerging 150 female fed for 6 days in hexane (3 ml) for two hours and sonicating
Lígia Miranda Ferreira Borges et al.
Veterinary parasitology, 147(1-2), 155-160 (2007-04-27)
This study was carried out with the objective of evaluating the efficacy of a 2,6-dichlorophenol (2,6-DCP) lure to control Dermacentor nitens (Acari: Ixodidae). Slow-release formulations of the pheromone formulated with and without cypermethrin were prepared. Olfactometer bioassays were used to
Davide Vione et al.
Chemosphere, 69(10), 1548-1554 (2007-07-10)
2,4-Dichlorophenol (2,4-DCP) and 2,6-dichlorophenol (2,6-DCP) undergo oxidation, nitrosation and nitration in the presence of nitrate under UV irradiation. Nitration is favoured under acidic conditions, most likely because HNO(2) is formed on nitrate photolysis. The most likely photonitration pathway is the
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