D70201
2,6-二氯苯酚
99%
别名:
2,6-二氯苯酚
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关于此项目
线性分子式:
Cl2C6H3OH
化学文摘社编号:
分子量:
163.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-761-3
Beilstein/REAXYS Number:
1447806
MDL number:
产品名称
2,6-二氯苯酚, 99%
InChI key
HOLHYSJJBXSLMV-UHFFFAOYSA-N
InChI
1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H
SMILES string
Oc1c(Cl)cccc1Cl
assay
99%
form
crystals
bp
218-220 °C (lit.)
mp
64-66 °C (lit.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
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
法规信息
危险化学品
此项目有
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:
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
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
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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