Skip to content
3-aminophenol

Structure via PubChem · Public domain (PubChem)

EntityQ779427· pop 18· linked from 8 articles

3-aminophenol

Sign in to save

Also known as m-hydroxyaniline

3-Aminophenol is an organic compound with formula C6H4(NH2)(OH). It is an aromatic amine and a phenol. It is the meta isomer of 2-aminophenol and 4-aminophenol.

In the Vinony graph

Within Vinony's link graph, 3-aminophenol is referenced by 8 other articles, and connects out to chlorine, International Standard Book Number and mass density.

Vinony files it under Aminophenols, Chembox having GHS data and ECHA InfoCard ID from Wikidata.

Its subject is documented across 17 Wikipedia language editions.

Chemical data

Formula
C6H7NO
Molecular weight
109.13 g/mol
IUPAC name
3-aminophenol
SMILES
C1=CC(=CC(=C1)O)N
InChIKey
CWLKGDAVCFYWJK-UHFFFAOYSA-N
XLogP
0.2
Polar surface area
46.3 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
hydrogen
Mass
109.053
Show 4 more facts
Commons category
3-Aminophenol
chemical formula
C₆H₇NO
canonical SMILES
C1=CC(=CC(=C1)O)N
melting point
124
Sources (1)

via Wikidata · CC0

~1 min read

Encyclopedic overview

3 sections
Contents
  • Preparation
  • Uses
  • References

3-Aminophenol is an organic compound with formula C6H4(NH2)(OH). It is an aromatic amine and a phenol. It is the meta isomer of 2-aminophenol and 4-aminophenol.

==Preparation== 3-Aminophenol is prepared by reduction of 3-nitrophenol. It can also be prepared by caustic fusion of 3-aminobenzenesulfonic acid (i.e. heating with NaOH to 245 °C for 6 hours) or from resorcinol via a substitution reaction with ammonium hydroxide.

Excerpted from Wikipedia’s “3-aminophenol” article, available under the CC BY-SA 4.0 licence.

Connections

Categories