Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

129364

Sigma-Aldrich

4-Iodoaniline

98%

Synonym(s):

p-Iodoaniline

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

About This Item

Linear Formula:
IC6H4NH2
CAS Number:
540-37-4
Molecular Weight:
219.02
Beilstein/REAXYS Number:
774101
EC Number:
208-743-4
MDL number:
MFCD00007848
UNSPSC Code:
12352100
PubChem Substance ID:
24847899
NACRES:
NA.22

assay

98%

form

solid

mp

61-63 °C (lit.)

solubility

H2O: slightly soluble
alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble

functional group

iodo

SMILES string

Nc1ccc(I)cc1

InChI

1S/C6H6IN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

InChI key

VLVCDUSVTXIWGW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

4-Iodoaniline is the most potent methaemoglobin former.

Application

4-Iodoaniline was used to prepare phenyl functionalized graphene oxide (I-Ph-GO).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF2858V
0000239397
WXBF0506V
STBK9720
STBK1238

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Ok-Kyung Park et al.
Nano letters, 12(4), 1789-1793 (2012-01-21)
Highly conductive reduced graphene oxide (GO) polymer nanocomposites are synthesized by a well-organized in situ thermochemical synthesis technique. The surface functionalization of GO was carried out with aryl diazonium salt including 4-iodoaniline to form phenyl functionalized GO (I-Ph-GO). The thermochemically
R Mahmud et al.
Toxicology, 117(1), 1-11 (1997-02-14)
The structural basis of dapsone (4,4'-diaminodiphenyl sulphone) haemotoxicity has been determined by investigation of the in vitro bioactivation of a series of 4-substituted arylamines. In the presence of rat liver microsomes, dapsone (100 microM) was the most potent former of
H Yoshida et al.
The Biochemical journal, 248(1), 79-84 (1987-11-15)
Azopigments were obtained from the delta fraction of bilirubin (mammalian biliprotein) in cholestatic sera of men, rats and guinea pigs by diazo reaction with diazotized p-iodoaniline and analysed by t.l.c. Delta bilirubin of men and rats generated both unconjugated and
J C Sinclair et al.
Protein expression and purification, 12(3), 371-380 (1998-05-16)
The N-hydroxyarylamine O-acetyltransferase from Salmonella typhimurium has been expressed as a histidine-tagged fusion protein in Escherichia coli and purified to apparent homogeneity using single-step immobilized metal ion chromatography. Sufficient quantities of the purified protein have been obtained to allow its
Reetendra Singh et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 20(13), 1728-1737 (2019-05-09)
Covalently cross-linked heterostructures of 2D materials are a new class of materials which possess electrochemical and photochemical hydrogen evolution properties. It was of considerable interest to investigate the role of interlayer spacing in the nanocomposites involving MoS2 and graphene sheets
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