131326
五氯苯
96%
别名:
1,2,3,4,5-Pentachlorobenzene
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线性分子式:
HC6Cl5
化学文摘社编号:
分子量:
250.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-172-0
Beilstein/REAXYS Number:
1911550
MDL number:
产品名称
五氯苯, 96%
InChI key
CEOCDNVZRAIOQZ-UHFFFAOYSA-N
InChI
1S/C6HCl5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H
SMILES string
Clc1cc(Cl)c(Cl)c(Cl)c1Cl
assay
96%
form
solid
bp
275-277 °C (lit.)
mp
84-87 °C (lit.)
density
1.609 g/mL at 25 °C (lit.)
functional group
chloro
Quality Level
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General description
水样中的五氯苯是通过直接与程序升温蒸发器-气相色谱-质谱联用的填充吸附剂（MEPS）测定的。
Application
用五氯苯通过光解法制备四氯苯。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
监管及禁止进口产品
此项目有
Synthesis of bridgehead fluorides by fluorodeiodination.
Della EW and Head NJ. et al.
The Journal of Organic Chemistry, 57(10), 2850-2855 (1992)
Gloria Grueiro Noche et al.
Analytical and bioanalytical chemistry, 405(21), 6739-6748 (2013-06-20)
A fully automated method consisting of microextraction by packed sorbent (MEPS) coupled directly to programmed temperature vaporizer-gas chromatography-mass spectrometry (PTV-GC-MS) has been developed to determine the 12 chlorobenzene congeners (chlorobenzene; 1,2-, 1,3-, and 1,4-dichlorobenzene; 1,2,3-, 1,2,4-, and 1,3,5-trichlorobenzene; 1,2,3,4-, 1,2,3,5-
Zhiqiang Nie et al.
Chemosphere, 85(11), 1707-1712 (2011-10-26)
Magnesium production is considered to be one potential source of unintentional persistent organic pollutants (unintentional POPs). However, studies on the emissions of unintentional POPs from magnesium metallurgy are still lacking. Emissions of unintentional POPs, such as polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), dioxin-like
Zhenzhen Xu et al.
Chemosphere, 87(9), 1032-1038 (2012-01-28)
Pentachlorobenzene (PeCB) in simulated flue gas was destructed by a commercial V(2)O(5)-WO(3)/TiO(2) catalyst in this study. The effects of reaction temperature, oxygen concentration, space velocity and some co-existing pollutants on PeCB conversion were investigated. Furthermore, a possible mechanism for the
Feng Xu et al.
Protein engineering, design & selection : PEDS, 20(10), 473-480 (2007-10-27)
We had reported engineering of the heme monooxygenase cytochrome P450cam from Pseudomonas putida with the F87W/Y96F/L244A/V247L mutations for the oxidation of pentachlorobenzene (PeCB), a recalcitrant environmental contaminant, to pentachlorophenol. In order to provide further insights into P450 structure, function and
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