63019-82-9

Usage

Uses

Used in Textile Industry:
N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline is used as a coloring agent for textiles, providing vibrant and long-lasting hues to fabrics. Its solubility in organic solvents facilitates its application in dyeing processes.
Used in Leather Industry:
In the leather industry, N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline serves as a dye, imparting color to leather goods. Its ability to produce a range of shades makes it a versatile choice for various leather products.
Used in Plastics Industry:
N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline is also utilized for coloring plastics, enhancing the visual appeal and customization options for plastic products.
Used in Biological Staining:
N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline finds application in biological staining, where it helps in the visualization of cellular structures under a microscope, aiding in research and diagnostics.
Used as a pH Indicator:
In laboratory settings, N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline functions as a pH indicator, assisting in the measurement and monitoring of acidity or alkalinity in various experiments.
Safety Precautions:
It is important to handle N,N-dimethyl-4-[(E)-pyridin-4-yldiazenyl]aniline with care, as it may pose health risks if ingested, inhaled, or comes into contact with skin and eyes. Proper safety measures should be taken during its use to minimize potential hazards.

Upstream product

• 504-24-5 4-aminopyridine 
• 138-89-6 p-dimethylaminonitrosobenzene 
• 100-23-2 N,N-Dimethyl-4-nitroaniline 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 1019107-33-5 1-benzyl-{4-[4-(N,N-dimethylaminophenyl)azo]}pyridinium chloride 
• 1019107-32-4 1-propyl-{4-[4-(N,N-dimethylaminophenyl)azo]}pyridinium bromide 
• 5169-64-2 1,1'-dihydroxy-2,2'-diphenyl-3,3'-biindole 

Relevant academic research and scientific papers

Molecular design of boronic acid-based dye receptors for nucleosides

Chromophric receptors for nucleosides were designed utilizing the boronic acid-diol interaction which effectively operates in aqueous solution. Receptors consist of a boronic acid moiety and a dimethylaminophenylazo moiety. The boronic acid moiety forms a

Structural Arrangement of 4-[4-(Dimethylamino)phenylazo]pyridine Push–Pull Molecules in Acidic Layered Hosts Solved by Experimental and Calculation Methods

4-[4-(dimethylamino)phenylazo]pyridine (further denoted as G) representing a type of push–pull molecules can be intercalated into α- and γ-modifications of zirconium phosphate (α-ZrP and γ-ZrP) and into zirconium (4-sulfophenyl)phosphonate (ZrSPP). The ob

COMPOUND FOR GENERATING SECOND HARMONIC OF LIGHT, DYE COMPOSITION FOR GENERATING SECOND HARMONIC OF LIGHT, AND CELL EXAMINATION METHOD

Provided are a compound that generates an SHG signal but has suppressed generation of a TPF signal. Also provided is a cell examination method using the same. A compound for generating a second harmonic of light, the compound being an azobenzene derivative of formula (1), or a salt thereof. (R1 and R2 independently represent alkyl groups having 6-12 carbon atoms, and R3 to R18 independently represent substituents selected from hydrogen, halogens, alkyl groups, alkoxy groups, aryl groups, amino groups, hydroxyl groups, nitro groups, and cyano groups, but R5 and R6, R9 and R10, R13 and R14, and R17 and R18 may combine together and form a ring structure having 5-7 carbon atoms. X represents —N+R19R20R21, a sulfonyl group, a carboxyl group, or an —OR group. Here, R19, R20, and R21 independently represent straight-chain or branched alkyl groups having 1-5 carbon atoms, and —OR represents a monovalent polyalkylene oxide group terminated by an alkoxy group. a is 0 or 1, b is 0 or 1, and n is an integer of 1-10.)

Light-controlled real time information transmitting systems based on nanosecond thermally-isomerising amino-azopyridinium salts

Aminoazopyridines are valuable molecules for stable information transmitting systems as well as for light-controlled optical oscillators. Amino-substituted azopyridinium methyl iodide salts transmit optical information within the time scale of nanoseconds, and moreover, show oscillation frequencies up to 1 MHz at room temperature.

Variable density effect of self-assembled polarizable monolayers on the electronic properties of silicon

Electronic structures at the Si/SiO2/molecule interfaces were studied by Kelvin probe techniques (contact potential difference) and compared to theoretical values derived by the Helmholtz equation. Two parameters influencing the electronic properties of n-type 〈100〉 Si/SiO 2 substrates were systematically tuned: the molecular dipole of coupling agent molecules comprising the layer and the surface coverage of the chromophoric layer. The first parameter was checked using direct covalent grafting of a series of trichlorosilane-containing coupling agent molecules with various end groups causing a different dipole with the same surface number density. It was found that the change in band bending (ΔBB) clearly indicated a major effect of passivation due to two-dimensional polysiloxane network formation, with minor differences resulting from the differences in the end groups' capacity to act as electron traps . The change in electron affinity (ΔEA) parameter increased upon increasing the dipole of the end group comprising the monolayer, resulting in a range of 600 mV. Moreover, a shielding effect of the aromatic spacer compared with the aliphatic spacer was found and estimated to be about 200 mV. The density effect was examined using the 4-[4-(N,N-dimethylamino phenyl)azo]pyridinium halide chromophore which has a calculated dipole of more than 10 D. It was clearly shown that upon increasing surface chromophoric coverage an increase in the electronic effects on the Si substrate was observed. However, a major consequence of depolarization was also detected while comparing the experimental and calculated values.

Langmuir-Blodgett film and second harmonic generation of a new type of amphiphilic non-linear optical bis-chromophore complex dye

A bivalent zinc complex anion: bis(2-thione-1,3-dithiol-4,5-dimercapto)zinc, has been chosen to balance several non-linear optical (NLO) dye cations in the design and synthesis of a series of novel bis-chromophore complex dyes. The Langmuir film-forming properties of these new NLO complex dyes at the air/water interface, the stability and second-order non-linear optical properties of the monolayer and Langmuir-Blodgett multilayer films were investigated. Results show that both the film-forming properties and NLO coefficiencies were improved greatly when the zinc complex anion was incorporated into four types of NLO-active organic dyes.