131857
1,2,4,5-Tetrachlorbenzol
98%
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About This Item
Empirische Formel (Hill-System):
C6H2Cl4
CAS-Nummer:
Molekulargewicht:
215.89
Beilstein:
1618315
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
98%
Form
chips
bp
240-246 °C (lit.)
mp (Schmelzpunkt)
138-140 °C (lit.)
SMILES String
Clc1cc(Cl)c(Cl)cc1Cl
InChI
1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H
InChIKey
JHBKHLUZVFWLAG-UHFFFAOYSA-N
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Anwendung
1,2,4,5-Tetrachlorobenzene was used to study the environmental behavior of hexachlorobutadiene (HCBD).
Signalwort
Warning
H-Sätze
P-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
320.0 °F - closed cup
Flammpunkt (°C)
160 °C - closed cup
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Oxygen consumption of juvenile rainbow trout (Oncorhynchus mykiss) exposed to sublethal concentrations of 1,2,4,5-tetrachlorobenzene and tetrachloroguaiacol.
R Yang et al.
Bulletin of environmental contamination and toxicology, 59(3), 479-485 (1997-09-01)
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