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D70201

Sigma-Aldrich

2,6-Dichlorophenol

99%

Sinónimos:

2,6-Dichlorophenol

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About This Item

Fórmula lineal:
Cl2C6H3OH
Número de CAS:
87-65-0
Peso molecular:
163.00
Beilstein/REAXYS Number:
1447806
EC Number:
201-761-3
MDL number:
MFCD00002176
UNSPSC Code:
12352100
PubChem Substance ID:
24894072
NACRES:
NA.22

assay

99%

form

crystals

bp

218-220 °C (lit.)

mp

64-66 °C (lit.)

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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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_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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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
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
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:
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