推荐产品
等级
analytical standard
产品线
PESTANAL®
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
沸点
218-220 °C (lit.)
mp
64-66 °C (lit.)
应用
agriculture
environmental
包装形式
neat
SMILES字符串
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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相关类别
一般描述
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.
应用
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
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
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
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
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
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
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
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