D70201
2,6-Dichlorophenol
99%
Synonym(s):
2,6-Dichlorophenol
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About This Item
Linear Formula:
Cl2C6H3OH
CAS Number:
Molecular Weight:
163.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-761-3
Beilstein/REAXYS Number:
1447806
MDL number:
Assay:
99%
Form:
crystals
Quality Level
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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Related Categories
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
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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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
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
Brancilene Santos de Araujo et al.
Chemosphere, 63(4), 642-651 (2005-12-21)
Hairy root cultures of Daucus carota L., Ipomoea batatas L. and Solanum aviculare Forst were investigated for their susceptibility to the highly toxic pollutants phenol and chlorophenols and for the involvement of inherent peroxidases in the removal of phenols from
Fabio Pezzotti et al.
Biotechnology progress, 20(6), 1868-1871 (2004-12-04)
Degradation of 2,6-dichlorophenol (2,6-DCP) was accomplished by oxidation catalyzed by Coprinus cinereus peroxidase. Immobilization of the enzyme in a polyacrylamide matrix enhanced DCP oxidation. Hydrogen peroxide, peroxidase's natural substrate, was produced enzymatically in situ to avoid peroxidase inactivation by its
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
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