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Product Information

Basic information about this product

Article No. 001573
Grade Synthesis
Purity 98%
CAS No. 60-09-3
Molecular Formula C12H12N3
Molecular Weight 197.24
H.S. Code 29270010
Shelf Life 60 Months

Hazard Information

Safety and hazard classification

GHS08 GHS08
GHS09 GHS09
Hazard Symbols
GHS08, GHS09

Safety Information

Important safety instructions and precautions

Signal Word: Danger
UN No.: 3077
IMCO Class No.: 9
Packing Group: III
Hazardous Statement: H350-H410
Precaution Statement: P201-P273-P308 + P313-P501

Product Description

Detailed information about the product

Product Overview

4-Aminoazobenzene 98% For Synthesis (CAS No. 60-09-3) is an aromatic azo compound consisting of an azobenzene chromophore bearing a primary amino group in the para position. Conjugation across the phenyl rings and azo linkage gives the molecule its characteristic chromophoric behaviour, while the amino functionality provides a reactive site for diazotisation, condensation, acylation, and other derivatisation reactions. This combination makes 4-aminoazobenzene a versatile intermediate for extending conjugated structures and preparing functional azo compounds.

The Synthesis grade is intended for preparative organic chemistry, dye-intermediate research, and the development of amino-functionalised azobenzene derivatives. It is suitable for reaction sequences involving modification of the para-amino group, formation of additional azo linkages, preparation of Schiff bases, and synthesis of conjugated compounds for chemical and materials-related investigations.

Typical Applications

  • Intermediate for the synthesis of azo, diazo, and related colour-forming compounds
  • Diazotisation followed by coupling to prepare disazo and extended azo structures
  • Preparation of selected acid-yellow and induline-type dye intermediates
  • Condensation with suitable aldehydes to produce azobenzene-containing Schiff bases
  • Synthesis of ligands and coordination compounds derived from aminoazobenzene structures
  • Functionalisation of the para-amino group to prepare substituted azo derivatives
  • Research involving azo chromophores and conjugated aromatic compounds
  • Preparative organic-chemistry studies requiring an amino-functionalised azobenzene building block

4-Aminoazobenzene is recognised as a dye intermediate and chemical building block, while published synthetic work documents its use in diazotisation–coupling sequences and Schiff-base preparation.

Common Synonyms

  • p-Aminoazobenzene
  • Aminoazobenzene
  • 4-Phenylazoaniline
  • 4-(Phenylazo)aniline
  • 4-(Phenyldiazenyl)aniline
  • Benzenamine, 4-(phenyldiazenyl)-
  • Azobenzene, 4-amino-
  • Aniline Yellow
  • C.I. Solvent Yellow 1
  • C.I. 11000

Storage Conditions

Store in a tightly closed container in a cool, dry, and well-ventilated location. Protect the material from direct light, excessive heat, moisture, and contamination. Minimise dust formation during dispensing and reseal the container promptly after use to preserve product quality.