Skip to Content
Merck
All Photos(2)

Key Documents

More Documents

180025

Sigma-Aldrich

3-Bromoaniline

98%

Synonym(s):

(3-Bromophenyl)amine, (m-Bromophenyl)amine, 1-Amino-3-bromobenzene, 3-Amino-1-bromobenzene, 3-Bromobenzenamine, m-Aminobromobenzene, m-Bromoaniline

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
BrC6H4NH2
CAS Number:
591-19-5
Molecular Weight:
172.02
Beilstein:
742028
EC Number:
209-704-4
MDL number:
MFCD00007757
UNSPSC Code:
12352100
PubChem Substance ID:
24850844
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.625 (lit.)

bp

251 °C (lit.)

mp

15-18 °C (lit.)

density

1.58 g/mL at 25 °C (lit.)

SMILES string

Nc1cccc(Br)c1

InChI

1S/C6H6BrN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2

InChI key

DHYHYLGCQVVLOQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

The in vitro nephrotoxic potential of 3-bromoaniline was studied.

Application

3-Bromoaniline was used in the synthesis of amino substituted quinazoline.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

446.0 °F

Flash Point(C)

> 230 °C

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

Cobb JM, et al.
Tetrahedron Letters, 40(5), 1045-1048 (1999)
G O Rankin et al.
Journal of applied toxicology : JAT, 15(2), 139-146 (1995-03-01)
Haloanilines are commonly used as chemical intermediates in the manufacture of a wide range of products. The purpose of this study was to examine the in vivo nephrotoxic and hepatotoxic potentials of the 3-haloanilines. The in vitro effects of the
Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12599-12602 (2012-09-05)
(C), its (O)K! An efficient palladium-catalyzed carbonylative synthesis of 2-alkylbenzoxazinones has been developed. By starting from 2-bromoanilines and acid anhydrides, the corresponding products were isolated in good yields.
L A Khawli et al.
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 19(3), 297-301 (1992-04-01)
Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoaniline was produced from the tin precursor, which was prepared using a palladium catalyzed reaction of hexabutylditin with m-bromoaniline. The radioiodinated BIA derivative is characterized by
Ali Sarafraz Yazdi et al.
Journal of chromatography. A, 1082(2), 136-142 (2005-07-23)
A novel method for the extraction of aromatic amines present in water samples is produced here coupling two-step liquid-phase microextraction with high performance liquid chromatography by using a monolithic column. The hydrophobic porous polypropylene membranes were used as the interface

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