arylamine

chemical compound

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Last updated

June 18, 2026

Quick Summary

An arylamine is a type of chemical compound that contains an amine group attached to an aryl group. Amines are organic compounds derived from ammonia, where one or more hydrogen atoms are replaced by organic substituents.12

Key characteristics of arylamines include:
* Structure: They have an aryl group (a cyclic, aromatic hydrocarbon group) directly bonded to the nitrogen atom of an amine group. A common example is aniline, where a phenyl group is attached to the amino nitrogen.13
* Properties: Like other amines, arylamines can have distinct odors, though their physical properties vary. Aromatic amines are generally denser than water. Some arylamines, like aniline, can be toxic and have been linked to health issues such as cancer.2
* Uses: Arylamines are important in the synthesis of various products, including dyes, pesticides, and synthetic fibers like Kevlar. They are also used in photography and as antioxidants. Aryl diazonium ions, derived from primary aromatic amines, are useful in preparing aryl halides.45

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bladder cancer
Risk Factors, Causes, and symptoms
…class of organic chemicals called arylamines is another significant risk factor. People who work in the leather, rubber, printing, and textiles industries or with large quantities of paint are often exposed to these chemicals and should exercise caution in their use. Other risk factors include those associated with lifestyle, such…
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…class of organic chemicals called arylamines is another significant risk factor. People who work in the leather, rubber, printing, and textiles industries or with large quantities of paint are often exposed to these chemicals and should exercise caution in their use. Other risk factors include those associated with lifestyle, such…
Read More

phenol
General synthesis of phenols
…is the diazotization of an arylamine (a derivative of aniline, C₆H₅NH₂) to give a diazonium salt, which hydrolyzes to a phenol. Most functional groups can survive this technique, as long as they are stable in the presence of dilute acid.
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…is the diazotization of an arylamine (a derivative of aniline, C₆H₅NH₂) to give a diazonium salt, which hydrolyzes to a phenol. Most functional groups can survive this technique, as long as they are stable in the presence of dilute acid.
Read More