131857
1,2,4,5-四氯苯
98%
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关于此项目
经验公式（希尔记法）:
C6H2Cl4
化学文摘社编号:
分子量:
215.89
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-466-2
Beilstein/REAXYS Number:
1618315
MDL number:
Assay:
98%
Form:
chips
InChI key
JHBKHLUZVFWLAG-UHFFFAOYSA-N
InChI
1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H
SMILES string
Clc1cc(Cl)c(Cl)cc1Cl
assay
98%
form
chips
bp
240-246 °C (lit.)
mp
138-140 °C (lit.)
Quality Level
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Application
1,2,4,5-四氯苯用于研究六氯丁二烯 (HCBD) 的环境行为 。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
320.0 °F - closed cup
flash_point_c
160 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
此项目有
Haiyan Zhang et al.
Environmental science & technology, 48(3), 1525-1531 (2014-01-10)
Although hexachlorobutadiene (HCBD) was recently proposed as a candidate persistent organic pollutant (POP) under the Stockholm Convention, information about its environmental levels and distributions is still very limited. In this work, HCBD was determined in the sewage sludge from 37
S Beil et al.
European journal of biochemistry, 247(1), 190-199 (1997-07-01)
The bacterium, Burkholderia (previously Pseudomonas) sp. strain PS12, reported earlier to degrade 1,2,4-trichlorobenzene is shown here to utilize also 1,2,4,5-tetrachlorobenzene (Cl4-benzene) as a growth substrate. To investigate the possibility that this organism attacks Cl4-benzene with a chlorobenzene dioxygenase which concomitantly
Lin Xiao et al.
Environmental science & technology, 41(8), 2750-2755 (2007-05-31)
We observed that the presence of transition metal ion, Ag+, Cu2+, or Fe3+, at a concentration of 3 mg L(-1) increases sorption of two nonpolar hydrophobic organic compounds (HOCs), phenanthrene (PHEN), and 1,2,4,5-tetrachlorobenzene (TeCB) by 1.5-4 times to Gram-negative bacteria
Motoki Terashima et al.
Chemosphere, 57(6), 439-445 (2004-09-08)
Solubilizing abilities of aggregates of humic acid (HA) to chlorinated benzenes (CBs) were investigated by means of the apparent water solubility enhancement. Both the water solubilities of 1,4-dichlorobenzene (DCB) and 1,2,4,5-tetrachlorobenzene (TeCB) linearly increased with increasing concentration of HA above
S Beil et al.
Journal of bacteriology, 180(21), 5520-5528 (1998-10-29)
The TecA chlorobenzene dioxygenase and the TodCBA toluene dioxygenase exhibit substantial sequence similarity yet have different substrate specificities. Escherichia coli cells producing recombinant TecA enzyme dioxygenate and simultaneously eliminate a halogen substituent from 1,2,4,5-tetrachlorobenzene but show no activity toward benzene
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