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129364

4-Iodoaniline

Name: 4-Iodoaniline
Brand: ALDRICH

98%

Synonym(s):

p-Iodoaniline

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About This Item

Linear Formula:

IC₆H₄NH₂

CAS Number:

540-37-4

Molecular Weight:

219.02

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847899

EC Number:

208-743-4

Beilstein/REAXYS Number:

774101

MDL number:

MFCD00007848

Assay:

98%

Form:

solid

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Properties

Quality Level

100

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

Description

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

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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In situ synthesis of thermochemically reduced graphene oxide conducting nanocomposites.

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

Structural basis for the haemotoxicity of dapsone: the importance of the sulphonyl group.

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

Purification, characterization, and crystallization of an N-hydroxyarylamine O-acetyltransferase from Salmonella typhimurium.

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

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Global Trade Item Number

SKU	GTIN
129364-100G	04061838726155
129364-25G	04061838726162