Interesting facts
Interesting Facts about 2,6-Diethylaniline
2,6-Diethylaniline is an intriguing chemical compound that belongs to the family of aromatic amines. Here are some engaging aspects of this compound:
- Structure and Substitution: The compound features two ethyl groups attached to the aniline structure at the 2 and 6 positions of the benzene ring. This unique substitution pattern contributes to its specific chemical properties and reactivity.
- Applications: 2,6-Diethylaniline is primarily used in the synthesis of dyes and pigments, showcasing its importance in the textile and plastics industries. Furthermore, it is utilized in the production of rubber antioxidants, enhancing the durability and longevity of rubber products.
- Toxicological Profile: As with many aromatic amines, 2,6-diethylaniline should be handled with care. Exposure can lead to health concerns, and therefore, safety protocols are essential when working with this compound in a laboratory setting.
- Synthetic Pathway: Chemists often employ various methods to synthesize 2,6-diethylaniline, often starting from readily available precursors. Understanding these synthetic routes is crucial for any aspiring chemist interested in organic synthesis.
- Reactivity: The presence of the nitrogen atom in the amine group makes 2,6-diethylaniline a nucleophilic site. This reactivity allows for various chemical reactions, including electrophilic aromatic substitution and acylation processes, which are fundamental in organic chemistry.
Overall, 2,6-diethylaniline is a valuable compound with both industrial applications and a variety of intriguing properties that make it a subject of study in the fields of chemistry and materials science.
Synonyms
2,6-DIETHYLANILINE
579-66-8
Benzenamine, 2,6-diethyl-
2,6-Diethylbenzenamine
2-Amino-1,3-diethylbenzene
Aniline, 2,6-diethyl-
2,6-Diethyl aniline
2,6-Diethyl-aniline
2,6-diethylphenylamine
CCRIS 2688
HSDB 5699
2,6-Diethyl-Benzenamine
Benzamine, 2,6-diethyl-
EINECS 209-445-7
BRN 1423626
DTXSID6027218
AI3-26297
2,6-Diethyl-Benzamine
VT2234594H
2,6-Diethylbenzenamine, 9CI
DTXCID607218
2,6-DIETHYLANILINE [HSDB]
4-12-00-02841 (Beilstein Handbook Reference)
2,6Diethyl aniline
2,6Diethylbenzenamine
2,6-Diethylbenzamine
Aniline, 2,6diethyl
Benzenamine, 2,6diethyl
2,6-DEA
209-445-7
MFCD00007753
CAS-579-66-8
2,6 DIETHYLANILINE
UNII-VT2234594H
Diethylaminobenzene
2,6-diethylanilin
2.6-diethylaniline
2,6-Diethylaniline, 98%
(2,6-diethyl-phenyl)-amine
SCHEMBL262868
CHEMBL3184218
Tox21_202010
Tox21_300333
STL570693
AKOS000120339
CS-W018171
FD64331
NCGC00247995-01
NCGC00247995-02
NCGC00254454-01
NCGC00259559-01
AC-10108
DS-13621
D0476
NS00014202
EN300-20612
D77824
Q209276
2,6-Diethylaniline, PESTANAL(R), analytical standard
F0001-1508
Z104479240
InChI=1/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H
Solubility of 2,6-diethylaniline
2,6-diethylaniline, a substituted aniline compound, presents interesting solubility characteristics. Its solubility can be influenced by several factors
:As a result, 2,6-diethylaniline is generally:
Overall, the solubility behavior of 2,6-diethylaniline exemplifies the balance between its polar amino group and its nonpolar hydrocarbon components. As the saying goes, “like dissolves like,” and in the case of this compound, that principle sees it favoring organic over aqueous solutions.