Skip to Content
Merck
All Photos(4)

Documents

D39029

Sigma-Aldrich

1,4-Dibromobenzene

98%

Synonym(s):

1,4-Dibromobenzene, 1-Bromo-4-bromobenzene, p-Bromophenyl bromide, p-Dibromobenzene, p-Phenylene dibromide, para-Dibromobenzene

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C6H4Br2
CAS Number:
106-37-6
Molecular Weight:
235.90
Beilstein:
1904543
EC Number:
203-390-2
MDL number:
MFCD00000089
UNSPSC Code:
12352100
PubChem Substance ID:
24893795
NACRES:
NA.22

Assay

98%

form

crystals

bp

219 °C (lit.)

mp

83-87 °C (lit.)

density

1.841 g/mL at 25 °C (lit.)

SMILES string

Brc1ccc(Br)cc1

InChI

1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H

InChI key

SWJPEBQEEAHIGZ-UHFFFAOYSA-N

Gene Information

human ... CYP2A6(1548)
mouse ... Cyp2a5(13087)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Paolini et al.
Mutation research, 413(3), 205-217 (1998-07-04)
Murine S9 liver fractions isolated from mice fed 7.5 g kg-1 2(3)-tert-Butyl-4-hydroxyanisole (BHA) for 3 weeks were tested to determine: (a) the profile of both phase-I and phase-II xenobiotic metabolizing enzymes; (b) their ability to induce in vitro covalent binding
A Colacci et al.
Toxicology letters, 54(2-3), 121-127 (1990-12-01)
1,4-Dibromobenzene (1,4-DBB) was covalently bound to DNA from liver, kidney, lung and stomach of mice after intraperitoneal administration. The covalent binding index (CBI) value (23 in mouse liver) was typical of weak initiators. On the contrary, no interaction with DNA
Y Chaisuksant et al.
Ecotoxicology and environmental safety, 39(2), 120-130 (1998-03-27)
The growth rate reduction of mosquito fish (Gambusia affinis) fry was investigated with a range of sublethal exposure levels of four halobenzenes for 42 days. These compounds were found to produce growth rate reduction in mosquito fish fry at concentrations
Vijay Gupta et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(12), 2658-2665 (2019-12-04)
A new triazole-functionalized tetracarboxylic acid ligand (H4 L) has been synthesized and utilized for the fabrication of a 3D ZnII organic framework with a Zn4 (-COO)6 cluster as the secondary building unit. The framework exhibits very good thermal stability and
Jadwiga A Szymańska et al.
International journal of occupational medicine and environmental health, 15(4), 375-383 (2003-03-01)
The distribution, excretion and metabolism of 1,4-dibromobenzene (1,4-DBB) and 1,2-dibromobenzene (1,2-DBB), following a single intraperitoneal administration to female Wistar rats, were investigated using radiotracer 3H and GC-MS technique. The maximum level of 3H after 1,4-DBB administration was detected in all
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service