Aniline
Aniline, phenylamine or aminobenzene ({{carbon}}{{sub|6}}{{hydrogen}}{{sub|5}}{{nitrogen}}{{hydrogen}}{{sub|2}}) is an organic chemical compound which is a primary aromatic amine consisting of a benzene ring and an amino group. The chemical structure of aniline is shown at the right.
Uses
The great commercial value of aniline is due to the readiness with which it yields, directly or indirectly, valuable dyestuffs. The discovery of mauve in 1858 by William Perkin was the first of a series of dyestuffs which are now to be numbered by hundreds. Reference should be made to the articles dyeing, fuchsine, safranine, indulines, for more details on this subject. In addition to dyestuffs, it is a starting-product for the manufacture of many drugs, such as antipyrine, antifebrin, etc. Aniline is manufactured by reducing nitrobenzene with iron and hydrochloric acid and steam-distilling the product. The purity of the product depends upon the quality of the benzene from which the nitrobenzene was prepared. In commerce three brands of aniline are distinguished—aniline oil for blue, which is pure aniline; aniline oil for red, a mixture of equimolecular quantities of aniline and ortho- and para-toluidines; and aniline oil for safranine, which contains aniline and ortho-toluidine, and is obtained from the distillate (échappés) of the fuchsine fusion. Monomethyl and dimethyl aniline are colourless liquids prepared by heating aniline, aniline hydro-chloride and methyl alcohol in an autoclave at 220°. They are of great importance in the colour industry. Monomethyl aniline boils at 193-195°; dimethyl aniline at 192°.
Related Topics:
Dye - 1858 - William Perkin - Dyeing - Fuchsine - Safranine - Indulines
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~ Table of Content ~
| ► | Introduction |
| ► | Synthesis |
| ► | Properties |
| ► | Uses |
| ► | History |
| ► | Controversy |
| ► | External links |
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