1137-80-0

Basic information

• Product Name: N,N-Dimethyl-4-(4-pyridinyl)aniline
• Synonyms: 4-[4-(Dimethylamino)phenyl]pyridine;N,N-Dimethyl-4-(4-pyridinyl)aniline;Dimethyl-(4-pyridin-4-yl-phenyl)-amine
• CAS NO: 1137-80-0
• Molecular Formula: C₁₃H₁₄N₂
• Molecular Weight: 198.26
• Mol File: 1137-80-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 334°C at 760 mmHg
• Flash Point: 155.8°C
• Appearance: /
• Density: 1.066g/cm³
• Vapor Pressure: 0.000132mmHg at 25°C
• Refractive Index: 1.595
• CAS DataBase Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)
• EPA Substance Registry System: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)

Safety Data

• Hazardous Substances Data: 1137-80-0(Hazardous Substances Data)

Usage

Description

N,N-Dimethyl-4-(4-pyridinyl)aniline is a chemical compound with the molecular formula C13H15N. It is a derivative of aniline and is known for its versatility in various industrial and commercial applications.

Uses

Used in Dye and Pigment Production:
N,N-Dimethyl-4-(4-pyridinyl)aniline is used as a key intermediate in the synthesis of dyes and pigments, contributing to the coloration and stability of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, N,N-Dimethyl-4-(4-pyridinyl)aniline serves as a building block for the development of certain drugs, playing a crucial role in the creation of new medicinal compounds.
Used in Materials Science:
N,N-Dimethyl-4-(4-pyridinyl)aniline is utilized in the field of materials science, particularly in the manufacturing of polymers and plastics, where it enhances the properties of these materials.
It is important to handle N,N-Dimethyl-4-(4-pyridinyl)aniline with care, as it can be toxic if not used properly.

InChI:InChI=1/C13H14N2/c1-15(2)13-5-3-11(4-6-13)12-7-9-14-10-8-12/h3-10H,1-2H3

Upstream product

• 110-86-1 pyridine 
• 121-69-7 N,N-dimethyl-aniline 
• 98-88-4 benzoyl chloride 
• 707-74-4 (trichloromethyl)mesitylene 
• 28611-39-4 4-(dimethylamino)benzene-boronic acid 
• 19524-06-2 4-bromopyridine hydrochloride 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 5957-96-0 4-(4-chlorophenyl)pyridine 
• 68-12-2 N,N-dimethyl-formamide 
• 637-87-6 1-Chloro-4-iodobenzene 
• 1692-15-5 4-pyridylboronic acid 

Downstream Products

• 91779-24-7 1-(4'-nitrophenyl)-4-(4''-dimethylaminophenyl)pyridinium iodide 
• 91779-22-5 1-phenyl-4-(4'-dimethylaminophenyl)pyridinium chloride 
• 91779-23-6 1-(4'-chlorophenyl)-4-(4''-dimethylaminophenyl)pyridinium chloride 
• 91779-21-4 1-(4'-methoxyphenyl)-4-(4''-dimethylaminophenyl)pyridinium chloride 
• 175091-14-2 (C₅H₄N)2Re(CO)3(C₅H₄N)(C₆H₄)N(CH₃)2⁽¹⁺⁾ 
• 906061-18-5 (4-(4'-dimethylaminophenyl)pyridine)tungsten pentacarbonyl 

Relevant articles and documents

First synthesis of novel aminophenyl pyridinium-5-(hydroxybenzoyl)-hydrazonomethyl-2-oxothiazol-3-ide derivatives and evaluation of their anticancer activities

The first total synthesis for large-scale production and anticancer activity of novel aminophenylpyridinium-5-(hydroxybenzoyl)hydrazonomethyl-2-oxothiazol-3-ide (PBHT) (1) and its derivatives are reported. The chemical structure of PBHT was unambiguously

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Some reactions of pyridinium salts derived from trichloromethylarenes with N- and C-nucleophiles

The reaction of N-(4-pyridyl)pyridinium and 4-chloropyridinium salts obtained from 1-trichloromethyl-2,4,6-trimethylbenzene and pyridine with N-nucleophiles such as piperidine and morpholine and with C-nucleophiles such as N,N-dimethylaniline and indole proceeds through hetarylation and gives the corresponding 4-substituted pyridines. N-(α,α-Dichlorobenzyl)pyridinium and N,N'-(α-chlorobenzylidene)bispyridinium salts obtained from trichloromethylbenzene do not undergo hetarylation.

Fluorescent substrates for neurotransmitter transporters

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