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131849

Sigma-Aldrich

1,2,3,4-Tetrachlorobenzene

98%

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About This Item

Fórmula empírica (notación de Hill):
C6H2Cl4
Número de CAS:
634-66-2
Peso molecular:
215.89
Beilstein/REAXYS Number:
1910025
EC Number:
211-214-0
MDL number:
MFCD00000538
UNSPSC Code:
12352100
PubChem Substance ID:
24848037
NACRES:
NA.22

assay

98%

form

chunks

bp

254 °C/761 mmHg (lit.)

mp

42-47 °C (lit.)

functional group

chloro

SMILES string

Clc1ccc(Cl)c(Cl)c1Cl

InChI

1S/C6H2Cl4/c7-3-1-2-4(8)6(10)5(3)9/h1-2H

InChI key

GBDZXPJXOMHESU-UHFFFAOYSA-N

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Application

1,2,3,4-tetrachlorobenzene was used as a model compound to determine the chlorobenzenes (CBs) in soil samples. It was also used for rapid dechlorination of 1,2,3,4-tetrachlorodibenzo-p-dioxin (1,2,3,4-TeCDD).

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
0000217507
0000289036
0000242163
0000176353
BGBB7869

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Li Wang et al.
Journal of chromatography. A, 1256, 9-14 (2012-08-15)
A novel and simple analytical method for the determination of chlorobenzenes (CBs) in soil samples was developed using ultrasonic-assisted water extraction (UAWE) coupled with solvent bar microextraction (SBME). Four chlorobenzenes, 1,2,3-trichlorobenzene (1,2,3-TCB), 1,2,3,4-tetrachlorobenzene (1,2,3,4-TeCB), hexachlorobenzene (HCB), and 1-chloro-4-nitrobenzene (1-C-4-NB), were
Young-Beom Ahn et al.
FEMS microbiology ecology, 66(2), 271-281 (2008-07-22)
Dechlorination of spiked 1,2,3,4-tetrachlorodibenzo-p-dioxin (1,2,3,4-TeCDD) was investigated in sediment microcosms from three polychlorinated dibenzo-p-dioxin and dibenzofuran (CDD/F)-contaminated sites: River Kymijoki, Finland; Gulf Island Pond, Maine; and Lake Roosevelt, Washington. Dechlorination was stimulated by addition of electron donor and halogenated priming
Ken G Drouillard et al.
Bulletin of environmental contamination and toxicology, 93(5), 561-566 (2014-06-18)
A vial equilibration technique was used to estimate the fugacity capacities of food and feces samples for 1,2,3,4-tetrachlorobenzene (TCB). The method was calibrated using different volumes of n-octanol and by comparing the measured and predicted fugacity capacity (Zoct) of n-octanol
Kenichiro Inoue et al.
Chemosphere, 70(3), 349-357 (2007-09-18)
Adsorption characteristics of carbonaceous adsorbents were examined using 1,2,3,4-tetrachlorobenzene, naphthalene and 2,4,6-tribromophenol as adsorbates. The breakthrough and equilibrium adsorption characteristics were evaluated using laboratory-scale adsorption test equipment. A micropore volume of diameter less than 2 nm is the most important
K T Kitchin et al.
Toxicology, 26(3-4), 243-256 (1983-03-01)
To assess possible maternal hepatic and reproductive effects of this uncharged, low molecular weight, lipophilic chlorinated benzene 0, 100, 300 and 1000 mg/kg/day of 1,2,3,4-tetrachlorobenzene (TCB) was orally administered to pregnant rats on days 9-13 of gestation and the animals
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