354987-84-1

Usage

Chemical Structure

A benzene ring with two amine groups (NH2) at positions 1 and 4, a naphthalenyl group attached to the nitrogen at position 1, and a diphenyl group attached to the nitrogen at position 4.

Molecular Weight

360.45 g/mol

Appearance

Yellow to brown crystalline solid

Solubility

Soluble in organic solvents like ethanol, acetone, and dimethyl sulfoxide (DMSO)

Melting Point

Approximately 158-162°C

Boiling Point

Not readily available, but expected to be high due to the molecular size and complexity

Density

Not readily available, but expected to be higher than water due to the molecular size and complexity

Uses

Commonly used in the production of various polymers and plastics, as well as a dye and rubber chemical

Hazardous Properties

Exposure to 1,4-Benzenediamine, N-1-naphthalenyl-N,N'-diphenyl- can be hazardous, and it is important to handle it with care, following proper safety protocols and guidelines.

Safety Precautions

Wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat when handling 1,4-Benzenediamine, N-1-naphthalenyl-N,N'-diphenyl-. Ensure proper ventilation and avoid inhalation or skin contact.

Storage

Store in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep in a tightly sealed container to prevent contamination and degradation.

Environmental Impact

Not readily available, but due to its chemical structure, it may have the potential to be toxic to aquatic life and should be disposed of according to local regulations and guidelines.

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 90-30-2 N-phenyl-1-naphthylamine 
• 62-53-3 aniline 
• 138310-84-6 N-(4-bromophenyl)-N-phenyl-1-naphthylamine 
• 32047-92-0 N-(4-iodobenzene)-N-phenylacetamide 

Downstream Products

• 209980-47-2 N,N'-bis{4-[(1-naphtyl)phenylamino]phenyl}-N,N'-diphenylbenzidine 
• 1029634-35-2 C₈₇H₆₁N₅ 

Relevant academic research and scientific papers

Compound Containing Ring Linked Via Carbazole and Fluorene And Organic Electronic Element Using The Same, Terminal Thereof

The present invention refers to carbazole ring coupled polyarylenic backbone containing organic compound and formed electrical component, its terminal number under public affairs substrate. (by machine translation)

Compound Containing Ring Linked Via Carbazole and Fluorene And Organic Electronic Element Using The Same, Terminal Thereof

Provided in the present invention are a compound containing a ring formed by bonding carbazole and fluorine, an organic electric element using the same, and a terminal thereof. The compound of the present invention can act various roles in an organic electric element and a terminal. In addition, when being applied to an organic electric element and a terminal, the compound reduces a driving voltage of the element and increases light efficiency, service life, and stability of the element.

COMPOUNDS AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

Disclosed are new compounds and an organic light emitting diode using the same. The organic light emitting diode using the new compound according to the present invention exhibits excellent characteristics in terms of actuating voltage, light efficiency, and lifespan.

NEW COMPOUNDS AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

Disclosed are new compounds and an organic light emitting diode using the same. The organic light emitting diode using the new compound according to the present invention exhibits excellent characteristics in terms of actuating voltage, light efficiency, and lifespan.

Organic EL devices and production process thereof

An organic electroluminescent device comprising a light-emitting layer between a pair of electrodes, the light-emitting layer comprising a mixture of a hole-transporting material consisting of a tertiary amine compound, an electron-transporting material and a light-emitting additive material, in which the tertiary amine compound has two or more oxidation potentials determined by a cyclic voltammetry wherein a potential difference between the first oxidation potential and the second oxidation potential in the oxidation potentials is 0.22V or more, and a glass transition temperature of at least 100° C., and the electron-transporting material has a glass transition temperature of at least 100° C.