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Supelco

2,6-Dichlorphenol

PESTANAL®, analytical standard

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About This Item

Lineare Formel:
Cl2C6H3OH
CAS-Nummer:
87-65-0
Molekulargewicht:
163.00
Beilstein:
1447806
EG-Nummer:
201-761-3
MDL-Nummer:
MFCD00002176
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329753647
NACRES:
NA.24

Qualität

analytical standard

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

218-220 °C (lit.)

mp (Schmelzpunkt)

64-66 °C (lit.)

Anwendung(en)

agriculture
environmental

Format

neat

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

Allgemeine Beschreibung

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.

Anwendung

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

Rechtliche Hinweise

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

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

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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Analysenzertifikate (COA)

Lot/Batch Number
BCCL8154
BCCC4286
SZBD336XV
SZBD010XV
SZB7346XV

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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
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
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