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About This Item
Empirical Formula (Hill Notation):
C6H4Br2
CAS Number:
Molecular Weight:
235.90
EC Number:
203-574-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1904538
MDL number:
grade
reagent grade
vapor density
8.16 (vs air)
vapor pressure
5 mmHg ( 66 °C)
product line
Vetec™
assay
97%
refractive index
n20/D 1.608 (lit.)
bp
218-219 °C (lit.)
mp
−7 °C (lit.)
density
1.952 g/mL at 25 °C (lit.)
SMILES string
Brc1cccc(Br)c1
InChI
1S/C6H4Br2/c7-5-2-1-3-6(8)4-5/h1-4H
InChI key
JSRLURSZEMLAFO-UHFFFAOYSA-N
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
200.1 °F - closed cup
flash_point_c
93.40 °C - closed cup
target_organs
Respiratory system
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A Sapota et al.
Chemosphere, 39(13), 2229-2238 (1999-11-27)
The distribution, excretion and metabolism of 1,3-dibromobenzene following a single i.p. administration to rats 100 or 300 mg/kg was investigated using radiotracer [3H] and GC-MS technique. After 72 hours about 74 to 90% were excreted in urine. The highest radioactivity
J A Szymańska
Archives of toxicology, 71(1-2), 99-106 (1996-01-01)
Rats were used to study acute and subacute hepatotoxicity of 1,3-dibromobenzene (1,3-dBB). In the single-exposure experiment, maximum hepatic 1,3-dBB concentrations were found to occur 1 to 12 h after the exposure, depending on the dose. Maximum concentrations of covalently bound
J A Szymańska et al.
Journal of applied toxicology : JAT, 16(1), 35-41 (1996-01-01)
Various doses of dibromobenzene isomers (1,2-dBB, 1,3-dBB, 1,4-dBB) were administered (i.p.) to BALB mice. The levels of reduced glutathione (GSH) and malondialdehyde (MDA) in the liver, and glutamate-pyruvate transaminase (GPT) (EC.2.6.1.2) gamma-glutamyltransferase (gamma-GT) (EC.2.3.2.2) and triglycerides (TG) in the serum
J A Szymańska
Archives of toxicology, 72(2), 97-103 (1998-02-10)
Brominated benzenes appear in the environment and human tissues. Their detection in the environment may be as a result of their usage, e.g. hexabromobenzene (HBB), and as products of HBB degradation or metabolism. The aim of this study was to
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