82532-76-1

Basic information

• Product Name: 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE
• Synonyms: 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE;P-DIPHENYLAMINOBENZALDEHYDE-N,N-DIPHENYL-HYDRAZONE;4-Diphenylamino-benzaldehyde-N,N-diphenylhydrazone;1,1-Diphenyl-2-[4-(diphenylamino)benzylidene]hydrazine;Diphenyl[4-[(2,2-diphenylhydrazono)methyl]phenyl]amine;N,N-Diphenyl-4-(2,2-diphenylhydrazonomethyl)aniline;N,N-Diphenyl-4-[(2,2-diphenylhydrazono)methyl]benzenamine
• CAS NO: 82532-76-1
• Molecular Formula: C31H25N3
• Molecular Weight: 439.55
• Product Categories: electronic
• Mol File: 82532-76-1.mol

Chemical Properties

• Melting Point: 164-169 °C(lit.)
• Boiling Point: 595.754 °C at 760 mmHg
• Flash Point: 314.101 °C
• Appearance: /
• Density: 1.06 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.609
• CAS DataBase Reference: 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE(82532-76-1)
• EPA Substance Registry System: 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE(82532-76-1)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 82532-76-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE is used as a reagent in organic synthesis for the formation of hydrazones, which are important intermediates in the synthesis of various organic compounds.
Used in Chemical Analysis:
In the field of chemical analysis, 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE is used as a detection and quantification agent for aldehydes and ketones in various chemical reactions, providing a means to monitor and measure the presence of these compounds.
Used in Material Science:
4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE is employed in material science for the development of new materials, leveraging its unique chemical properties to create innovative substances with potential applications in various industries.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-(DIPHENYLAMINO)BENZALDEHYDE DIPHENYLHYDRAZONE is used in the research and development of new drugs, contributing to the discovery of novel therapeutic agents and advancing medicinal chemistry.

InChI:InChI=1/C31H25N3/c1-5-13-27(14-6-1)33(28-15-7-2-8-16-28)29-23-21-26(22-24-29)25-32-34(30-17-9-3-10-18-30)31-19-11-4-12-20-31/h1-25H/b32-25+

Upstream product

• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 530-47-2 N,N-diphenylhydrazine hydrochloride 
• 530-50-7 1,1-Diphenylhydrazine 

Relevant articles and documents

PROCESS FOR PRODUCING HYDRAZONE COMPOUND

The present invention provides a process for producing a hydrazone compound represented by the general formula (5): which comprises a step of condensing a hydrazine compound represented by the general formula (3): with a carbonyl compound represented by the general formula (4): without taking the hydrazine compound out of a reactor. According to the invention, the target hydrazone compound can be obtained in high quality and in a high yield without taking the hydrazine compound out of the reactor at all, the hydrazine compound being a reaction intermediate which is structurally unstable and has a fear of influencing safety of workers owing to its toxicity (mutagenicity).

CHARGE TRANSPORT PROPERTIES OF ARYLALDEHYDE HYDRAZONES IN THEIR GLASSY STATES - SINGLE COMPONENT AND DOPED SYSTEMS

For the purpose of elucidating charge transport in disordered organic materials, hole transport in the glassy state of 4-diphenylaminobenzaldehyde diphenylhydrazone (DPH), 4-diphenylaminobenzaldehyde methylphenylhydrazone (DPMH), and DPH doped with a small amount of 4-diethylaminobenzaldehyde diphenylhydrazone (DEH) has been studied.The hole drift mobility in the DPMH glass was approximately one-fifth of that in the DPH glass; this was attributed to a higher activation energy in terms of the Arrhenius formalism or to an increased width of the Gaussian density of states based on the site energy disorder model for the DPMH glass.The introduction of less than 1 molpercent DEH into DPH resulted in a significant increase in activation energy or in the Gaussian width of the site energy distribution, which increased with increasing concentration of the dopant. - Keywords: 4-diphenylaminobenzaldehyde diphenylhydrazone, 4-diphenylaminobenzaldehyde methylphenylhydrazone, 4-diethylaminobenzaldehyde diphenylhydrazone, mobility, charge transport, Poole Frenkel, photoconductivity, trapping

HOLE DRIFT MOBILITIES IN THE GLASSY STATE OF ARYLALDEHYDE AND ARYLKETONE HYDRAZONES

Hole transport in the glassy state of arylaldehyde and arylketone hydrazones, 4-diphenylaminobenzaldehyde diphenylhydrazone (DPH) and 4-diphenylaminoacetophenone diphenylhydrazone (M-DPH), has been studied.The values of the hole drift mobility in the glas