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4-Aminophthalonitrile
[CAS# 56765-79-8]

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Complete supplier list of 4-Aminophthalonitrile
Identification
Classification Chemical reagent >> Organic reagent >> Cyanide/nitrile
Name 4-Aminophthalonitrile
Synonyms 3,4-Dicyanoaniline; 4-Amino-1,2-benzenedicarbonitrile
Molecular Structure CAS # 56765-79-8, 4-Aminophthalonitrile, 3,4-Dicyanoaniline, 4-Amino-1,2-benzenedicarbonitrile
Molecular Formula C8H5N3
Molecular Weight 143.15
CAS Registry Number 56765-79-8
EC Number 260-370-6
SMILES C1=CC(=C(C=C1N)C#N)C#N
Properties
Melting point 177-182 ºC
Water solubility Insoluble
Safety Data
Hazard Symbols symbol symbol   GHS06;GHS07 Danger    Details
Hazard Statements H301-H311-H315-H319-H331-H335    Details
Precautionary Statements P261-P262-P264-P264+P265-P270-P271-P280-P301+P316-P302+P352-P304+P340-P305+P351+P338-P316-P319-P321-P330-P332+P317-P337+P317-P361+P364-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.3H311
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.3H331
Eye irritationEye Irrit.2AH319
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
4-Aminophthalonitrile, a chemical compound also known as 4-APN, was first discovered through organic chemistry research. Its synthesis involves the reaction of phthalonitrile with ammonia or an amine derivative. This discovery can be traced back to the late 20th century, with its structure confirmed via spectroscopic analysis and chemical characterization. The unique combination of an amino group and phthalonitrile structure makes 4-Aminophthalonitrile a valuable compound for various applications across different industries.

4-Aminophthalonitrile serves as a key intermediate in the synthesis of vat dyes, which are widely used in the textile industry for dyeing cotton and other natural fibers. It contributes to the vibrant and colorfast hues of textile products.

This compound is utilized as a building block in organic synthesis to produce various heterocyclic compounds and pharmaceutical intermediates. Its versatile reactivity enables the creation of complex molecules with diverse functionalities.

4-Aminophthalonitrile finds applications in materials science for the synthesis of functional materials, including polymers, resins, and coatings. It imparts specific properties such as thermal stability, electrical conductivity, and corrosion resistance to these materials.

Used as a starting material in pharmaceutical synthesis, 4-Aminophthalonitrile contributes to the production of pharmaceuticals targeting various therapeutic areas, including cardiovascular diseases, cancer treatments, and antimicrobial agents.

Researchers employ 4-Aminophthalonitrile in chemical research for studying reaction mechanisms and developing new synthetic routes. It serves as a valuable tool for exploring novel molecules and their potential applications in medicine, materials science, and other fields.
Market Analysis Reports
List of Reports Available for 4-Aminophthalonitrile
Related Products
4-Aminophthalhydrazide  3-Aminophthalhydrazide  3-Aminophthalic acid  4-Aminophthalic acid  3-Aminophthalic acid hydrochloride  4-Aminophthalide  5-Aminophthalide  6-Aminophthalide  3-Aminophthalimide  4-Aminophthalimide  o-Aminophthalylhydrazido-N-acetyl-beta-D-glucosaminide  Aminophylline  3-Amino-2-picoline  2-Amino-4-picoline  2-Amino-3-picoline  4-Amino-2-picoline  (+/-)-2-Aminopimelic acid  1-Aminopiperidine  4-(3-Aminophenyl)-2-pyrrolidinone hydrochloride  1-(4-Aminophenyl)-3-(1-pyrrolidino)-5-pyrazolone