2,4,6-Trimethylaniline, also known as mesidine, is a colorless liquid aromatic amine. It is an important precursor in the synthesis of various organic compounds, including dyes, pharmaceuticals, and pesticides. 2,4,6-Trimethylaniline is synthesized through the reduction of 2,4,6-trinitroanisole using a reducing agent like iron and hydrochloric acid. The compound is known for its ability to act as a weak base and can be used in the formation of salts with strong acids. Research on 2,4,6-trimethylaniline focuses on its potential applications in materials science, especially in the development of conductive polymers and organic semiconductors. Its unique electronic and structural properties make it a valuable component for developing new materials with advanced electrical conductivity and optical properties. The compound is also studied for its potential in catalysis and as a building block in the synthesis of complex organic molecules.'
2,4,6-trimethylaniline: RN given refers to parent cpd
ID Source | ID |
---|---|
PubMed CID | 6913 |
CHEBI ID | 82545 |
SCHEMBL ID | 139002 |
MeSH ID | M0061715 |
Synonym |
---|
BIDD:GT0806 |
88-05-1 |
2,4,6-trimethyl aniline |
mesitylamine |
einecs 201-794-3 |
mesidine |
2-amino-1,3,5-trimethylbenzene |
mesidin [czech] |
mesidin |
aminomesitylene |
2-aminomesitylene |
mesitylene, 2-amino- |
1-amino-2,4,6-trimethylbenzen [czech] |
2,4,6-trimethylbenzenamine |
ccris 2871 |
hsdb 2694 |
aniline, 2,4,6-trimethyl- |
nsc-31 |
2,4,6-trimethylaniline |
inchi=1/c9h13n/c1-6-4-7(2)9(10)8(3)5-6/h4-5h,10h2,1-3h |
benzenamine, 2,4,6-trimethyl- |
2,4,6-trimethylaniline, 98% |
AKOS000119132 |
C19540 |
(2,4,6-trimethyl-phenyl)-amine |
STL164356 |
2,4,6-trimethylphenylamine |
1-amino-2,4,6-trimethylbenzen |
unii-yir5crl5bg |
yir5crl5bg , |
FT-0609896 |
2,4,6-trimethylaniline [iarc] |
1-amino-2,4,6-trimethylbenzene |
2-amino-1,3,5-trimethylbenzene [hsdb] |
SCHEMBL139002 |
CHEBI:82545 |
DTXSID5043847 |
mesityl amine |
2,4,6-trimethyl-aniline |
2,4,6-trimethyl-phenylamine |
benzeneamine, 2,4,6-trimethyl- |
W-100422 |
STR00896 |
CS-W007785 |
F2190-0482 |
2,4,6-trimethylaniline (mesidine), nd25=1,4959 |
2,4,6-trimethylaniline, purum, >=98.0% (gc) |
mfcd00007740 |
Q4596776 |
AMY25805 |
CCG-302506 |
D77687 |
2-nitrophenyln-acetyl-alpha-dgalactosaminide |
EN300-19092 |
Z104472738 |
Class | Description |
---|---|
substituted aniline | |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 4 (50.00) | 18.7374 |
1990's | 3 (37.50) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (12.50) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.
| This Compound (36.98) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 9 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |