Diethylaniline Is an Organic Compound That Is Produced In Bulk and Is Used To Manufacture Chemical Dyes Such As Azo Dyes
Diethylaniline
is used all over the world, especially in a region such as the United States. Diethylaniline
(also known as N Dinthinoline or N Dexanol) is the first organic compound with
the correct molecular structure to be used in the synthesis of azo dyes. This
organic compound was isolated by Dr. Arnold K. Klement at the University of
California, Davis. Diethylaniline can be used in dye synthesis.
Diethylaniline was initially marketed under the trade names
Methylenediamine and Diethylenediamine. The reason why Diethylaniline was marketed
under these trade names is that it was intended to be used in the synthesis of
azo dyes. It was not intended to be used in the synthesis of colors it was
never designed as a colorless compound. Currently, clinical trials are being
conducted to test the safety and toxicity of this new organic compound. Based
on the results of these tests, Diethylaniline will become a prescription
cosmetic when the regulatory bodies approve its use.
Diethylaniline
has a molecular structure that is very similar to that of the coloring agent
ferricyanide. The similarities between the structure of Diethylaniline and that
of ferricyanide give rise to some similarities in the functional groups of the
molecules that make up the color of the compound. Diethylaniline is used widely
in textile industries. In regions such as the U.S., the prevalence of textile
industries has increased the usage of N-Diethylaniline. For instance, according
to the Textile Society of America, there are around 13,427 textile mills
businesses in the US currently.
When
Diethylaniline was introduced in the market as a colorless organic compound,
many cosmetic manufacturers saw its potential in a wide range of applications. Diethylaniline
showed exceptional photosensitivity, including blue lights, but photo-dispersive
properties and stability were much better than that of other organic dyes. It
showed comparable photo-chemical properties to ferricyanide, but it showed much
better stability than that of lutein-hydroxy acids. The stability of the color
resulted from the chemical structure of the n-diethyl group. C-C-base groups
form a linear molecular structure with one oxygen and three nitrogen atoms in
the center of the carbon chain. The four extra atoms on the side of the C-C
bond are hydrogen atoms.
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