Acetamide, N-(4-aminophenyl)-, hydrochloride

Cl.CC(=O)NC1=CC=C(N)C=C1

InChIKey=JWCADJJPGAITCH-UHFFFAOYSA-N

InChI=1S/C8H10N2O.ClH/c1-6(11)10-8-4-2-7(9)3-5-8;/h2-5H,9H2,1H3,(H,10,11);1H

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Acid violet 7 and its biodegradation products induce chromosome aberrations, lipid peroxidation, and cholinesterase inhibition in mouse bone marrow.	2010-08	20369386
Determination of p-phenylenediamine and its metabolites MAPPD and DAPPD in biological samples using HPLC-DAD and amperometric detection.	2009-06-01	19409864
In vitro mutagenicity of Acid Violet 7 and its degradation products by Pseudomonas putida mt-2: Correlation with chemical structures.	2009-03	21783945
Synthesis, IR, UV/vis-, (1)H NMR and DFT study of chelatophore functionalized 1,3-benzoxazinone spiropyrans.	2008-12-01	18550424
Molecular structure, spectroscopic studies and first-order molecular hyperpolarizabilities of p-amino acetanilide.	2008-11-15	18321771
Physical stability of amorphous acetanilide derivatives improved by polymer excipients.	2006-08	16880672
Oligomers of "extended viologen", p-phenylene-bis-4,4'-(1-aryl-2,6-diphenylpyridinium), as candidates for electron-dopable molecular wires.	2005-01-21	15651779
Transient resonance Raman and density functional theory investigation of the 4-acetamidophenylnitrenium ion.	2003-06-27	12816488

Patents

Substance Class	Chemical Created by `admin` on `Tue Apr 01 17:44:28 GMT 2025` Edited by `admin` on `Tue Apr 01 17:44:28 GMT 2025`
Record UNII	V7BJ5H4ZL6
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

Acetamide, N-(4-aminophenyl)-, hydrochloride

Common Name

English

Acetamide, N-(4-aminophenyl)-, monohydrochloride

Preferred Name

English

Acetamide, N-(4-aminophenyl)-, hydrochloride (1:1)

Systematic Name

English

Code System Code Type Description

ECHA (EC/EINECS)

256-052-1