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Merck

D70201

Sigma-Aldrich

2,6-Dichlorphenol

99%

Synonym(e):

2,6-Dichlorophenol

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About This Item

Lineare Formel:
Cl2C6H3OH
CAS-Nummer:
Molekulargewicht:
163.00
Beilstein:
1447806
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

99%

Form

crystals

bp

218-220 °C (lit.)

mp (Schmelzpunkt)

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

InChIKey

HOLHYSJJBXSLMV-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Corrosion

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Skin Corr. 1B

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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Kunden haben sich ebenfalls angesehen

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
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
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:
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
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

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