3007-75-8

Basic information

• Product Name: N,N-DI-N-OCTYLANILINE
• Synonyms: N,N-DI-N-OCTYLANILINE;N,N-Dioctylaniline;Dioctylphenylamine;N-Phenyldioctylamine
• CAS NO: 3007-75-8
• Molecular Formula: C₂₂H₃₉N
• Molecular Weight: 317.55
• Mol File: 3007-75-8.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 197-198°C 3mm
• Flash Point: >130°C
• Appearance: /
• Density: 0.885 g/cm³
• Vapor Pressure: 4.55E-07mmHg at 25°C
• Refractive Index: 1.5495
• PKA: 6.29±0.50(Predicted)
• CAS DataBase Reference: N,N-DI-N-OCTYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DI-N-OCTYLANILINE(3007-75-8)
• EPA Substance Registry System: N,N-DI-N-OCTYLANILINE(3007-75-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 3007-75-8(Hazardous Substances Data)

Usage

General Description

N,N-Di-N-octylaniline, also known as 2,2'-dianilino-1,1'-binaphthyl, is a chemical compound commonly used as a dye intermediate and in the manufacture of various colorants and pigments. It is a member of the family of diarylanilines, which are important building blocks in organic synthesis. N,N-Di-N-octylaniline is also used as a color developer in the production of color photographic materials and as a stabilizer in the production of plastics and rubber. It is a clear, light yellow to brown liquid with a characteristic odor, and it is insoluble in water but soluble in organic solvents. The chemical is considered to have low toxicity and is not expected to bioaccumulate in the environment.

InChI:InChI=1/C22H39N/c1-3-5-7-9-11-16-20-23(22-18-14-13-15-19-22)21-17-12-10-8-6-4-2/h13-15,18-19H,3-12,16-17,20-21H2,1-2H3

Upstream product

• 621-06-7 2,N-diphenylacetamide 
• 124-07-2 Octanoic acid 
• 62-53-3 aniline 
• 111-87-5 octanol 
• 98-95-3 nitrobenzene 
• 111-83-1 1-bromo-octane 
• 14866-33-2 tetraoctyl ammonium bromide 
• 3007-71-4 N-octylaniline 

Downstream Products

• 93523-79-6 C₃₉H₅₀NO⁽¹⁺⁾*ClO₄^(1-) 
• 149796-15-6 6-(1,3-dioxoindan-2-ylidene)-2-oxo-3-(4-N,N-dioctylaminophenyl)-2,6-dihydrobenzofuran 
• 174420-65-6 3-[4-(N,N-dioctylamino)phenyl]-4-hydroxycyclobutene-1,2-dione 
• 933037-93-5 4-[(1E)-2-(4-iodophenyl)ethenyl]-N,N-dioctylbenzenamine 
• 497151-94-7 4-N,N-dioctylamino-4'-formyl-2'-nitroazobenzene 
• 193154-07-3 4-(N,N-dioctylamino)-4'-trifluoroacetylazobenzene 
• 174420-64-5 1-chloro-2-(p-dioctylaminophenyl)cyclobutene 3,4-dione 

Relevant articles and documents

NOVEL CATHODE BUFFER LAYER MATERIAL AND ORGANIC PHOTOELECTRIC DEVICE INCLUDING SAME

The present invention relates to a novel cathode buffer layer material and an organic photoelectric device including the same. When the novel compound of the present invention is applied to a cathode buffer layer of an organic photoelectric device, for example, an organic solar cell or an organic photodiode, there is an effect in which the surface characteristics of an electron transport layer are improved through the high dipole moment of the novel compound to thereby facilitate electron extraction from a photoactive layer to a cathode electrode and to reduce series resistance and leakage current, and accordingly, the performance of an organic optoelectronic device (organic solar cell, organic photodiode, etc.) to be manufactured can be remarkably improved, which is industrially advantageous.

Iridium-Catalyzed Alkylation of Amine and Nitrobenzene with Alcohol to Tertiary Amine under Base- and Solvent-Free Conditions

Herein, an efficient and green method for the selective synthesis of tertiary amines has been developed that involves iridium-catalyzed alkylation of various primary amines with aromatic or aliphatic alcohols. Notably, the catalytic protocol enables this transformation in the absence of additional base and solvent. Furthermore, the alkylation of nitrobenzene with primary alcohol to tertiary amine has also been achieved by the same catalytic system. Deuterium-labeling experiments and a series of control experiments were conducted, and the results suggested that an intermolecular borrowing hydrogen pathway might exist in the alkylation process.

Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen

A convenient, practical and green N-alkylation of amines has been accomplished by applying readily available carboxylic acids in the presence of molecular hydrogen. Applying an in situ formed ruthenium/triphos complex and an organic acid as cocatalyst, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields. This novel method is also successfully applied for the synthesis of unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling reaction of the corresponding amines, carboxylic acids, and CO2 as a C1 source.