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Merck
CN

D70201

2,6-Dichlorophenol

99%

Synonym(s):

2,6-Dichlorophenol

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About This Item

Linear Formula:
Cl2C6H3OH
CAS Number:
87-65-0
Molecular Weight:
163.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894072
EC Number:
201-761-3
Beilstein/REAXYS Number:
1447806
MDL number:
MFCD00002176

Key Documents

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Product Name

2,6-Dichlorophenol, 99%

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

assay

99%

form

crystals

bp

218-220 °C (lit.)

mp

64-66 °C (lit.)

Quality Level

200

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Related Categories

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
0000336354
MKCW2231
0000336354
0000279367
MKCS9444

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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
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
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
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
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