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Merck

31102

Supelco

2,6-二氯苯酚

PESTANAL®, analytical standard

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About This Item

线性分子式:
Cl2C6H3OH
CAS号:
分子量:
163.00
Beilstein:
1447806
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

bp

218-220 °C (lit.)

mp

64-66 °C (lit.)

應用

agriculture
environmental

格式

neat

SMILES 字串

Oc1c(Cl)cccc1Cl

InChI

1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H

InChI 密鑰

HOLHYSJJBXSLMV-UHFFFAOYSA-N

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相关类别

一般說明

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.

應用

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

法律資訊

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

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

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

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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
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
Qiang He et al.
Applied microbiology and biotechnology, 65(4), 377-382 (2004-06-05)
A continuous fed-batch reactor system was developed to rapidly obtain dense chlororespiring cultures of Anaeromyxobacter dehalogenans strain 2CP-C. A syringe pump continuously delivered concentrated 2,6-dichlorophenol (50-150 mM) to an anaerobic reactor vessel at a rate that sustained linear growth but

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