2,4,6-trimethylaniline
Structural formula | |||||||||||||||||||
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Surname | 2,4,6-trimethylaniline | ||||||||||||||||||
other names |
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Molecular formula | C 9 H 13 N | ||||||||||||||||||
Brief description |
yellow-brown liquid with a characteristic odor |
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properties | |||||||||||||||||||
Molar mass | 135.21 g mol −1 | ||||||||||||||||||
Physical state |
liquid |
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density |
0.96 g cm −3 (20 ° C) |
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Melting point |
−5 ° C |
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boiling point |
232-234 ° C |
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solubility |
practically insoluble in water |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2,4,6-Trimethylaniline ( mesidine ) is an aromatic amine with three methyl groups (-CH 3 ) and one amino group (-NH 2 ) as substituents on the benzene ring . It belongs to the trimethylaniline group of substances . The common name mesidine is derived from mesitylene ( sym. Trimethylbenzene).
history
Mesidine was described by August Wilhelm von Hofmann in 1875 .
Extraction and presentation
2,4,6-Trimethylaniline is produced by nitration of mesitylene and subsequent reduction.
use
2,4,6-Trimethylaniline is used as an intermediate in the production of anthraquinone dyes , pharmaceuticals and azo polymerization initiators .
Individual evidence
- ↑ a b c d e f g h Entry on 2,4,6-trimethylaniline in the GESTIS substance database of the IFA , accessed on July 23, 2016(JavaScript required) .
- ^ AW Hofmann : Note on mesidine . In: Reports of the German Chemical Society . tape 8 , no. 1 , January 1875, p. 61–62 , doi : 10.1002 / cber.18750080119 ( PDF ).
- ↑ a b entry on mesidine. In: Römpp Online . Georg Thieme Verlag, accessed on November 20, 2014.
Web links
Commons : 2,4,6-Trimethylaniline - Collection of Pictures, Videos, and Audio Files