3007-75-8

Usage

Uses

Used in Chemical Synthesis:
N,N-Di-N-octylaniline is used as a dye intermediate for the production of various colorants and pigments, contributing to the vibrant color palettes in different industries.
Used in Color Photography:
In the color photography industry, N,N-Di-N-octylaniline is used as a color developer, playing a crucial role in the creation of color photographic materials.
Used in Plastics and Rubber Industry:
N,N-Di-N-octylaniline is utilized as a stabilizer in the production of plastics and rubber, enhancing the durability and performance of these materials.
Used in Organic Synthesis:
As a member of the diarylaniline family, N,N-Di-N-octylaniline is used as a building block in organic synthesis, facilitating the development of new organic compounds and materials.

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

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

Downstream Products

• 193154-07-3 4-(N,N-dioctylamino)-4'-trifluoroacetylazobenzene 
• 497151-94-7 4-N,N-dioctylamino-4'-formyl-2'-nitroazobenzene 
• 149796-15-6 6-(1,3-dioxoindan-2-ylidene)-2-oxo-3-(4-N,N-dioctylaminophenyl)-2,6-dihydrobenzofuran 
• 93523-79-6 C₃₉H₅₀NO⁽¹⁺⁾*ClO₄^(1-) 
• 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 
• 174420-64-5 1-chloro-2-(p-dioctylaminophenyl)cyclobutene 3,4-dione 

Relevant academic research and scientific papers

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.

Compound and preparation method thereof, and application of compound as n-type dopant

The invention provides a compound and a preparation method thereof, and application of the compound as an n-type dopant. The structural formula of the compound is shown as a formula (I) which is described in the specification. The compound can be used as

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.

Method of producing higher amine (by machine translation)

PROBLEM TO BE SOLVED: To provide a method of producing a secondary or tertiary higher amine. SOLUTION: The method of producing a higher amine comprises allowing a primary or secondary amine to react with an alcohol in the presence of at least one species of hydrogen halide selected from hydrogen chloride, hydrogen bromide and hydrogen iodide, or in the presence of a compound capable of producing a hydrogen halide (such as 1,3,5-triazo-2,4,6-triphosphorine-2,2,4,4,6,6-chloride). If the raw material amine is a primary amine, a secondary higher amine and a tertiary higher amine can be produced. If the raw material amine is a secondary amine, a tertiary higher amine can be produced. COPYRIGHT: (C)2012,JPO&INPIT

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.

Cruciform 9,10-distyryl-2,6-bis(p-dialkylamino-styryl)anthracene homologues exhibiting alkyl length-tunable piezochromic luminescence and heat-recovery temperature of ground states

A series of 2,6-bis(p-dialkylaminostyryl)-9,10-distyrylanthracene (FCn) cruciforms with N-alkyl chains of different lengths have been synthesized, and their aggregation-enhanced fluorescence and piezochromic luminescence (PFC) behaviours are investigated. These 9,10-distyrylanthracene-containing cruciforms exhibit relatively low fluorescence quantum yields (Φ) in THF solution (Φ ≈ 10%) and moderate aggregation-enhanced emission in aqueous media (Φ ≈ 25%), but strong and chain length-dependent solid-state fluorescence emission. Grinding and pressing experiments indicate that they are all effective PFC materials in terms of mechanical stress-induced spectral shifts (ΔλPFC = 23-54 nm), moreover, the longer alkyl-containing FCn shows a larger ΔλPFC. Powder X-ray diffraction and differential scanning calorimetry measurements reveal that the transformation between the crystalline and amorphous states upon external stimuli is responsible for the reversible PFC behaviour. It is found that increasing the N-alkyl length could effectively decrease the cold-crystallization temperature of the ground states to render the PFC states with a tunable heat-recovering temperature, and ground FC10 and FC12 solids can recover spontaneously to their original states at room temperature.

Direct one-pot reductive N-alkylation of nitroarenes by using alcohols with supported gold catalysts

Gold standard support! The direct reductive mono- or di-N-alkylation of aromatic nitro compounds with alcohols, using a hydrogen-borrowing strategy, was efficiently promoted by a ligand-free titania-supported gold catalyst system (see scheme). A variety of nitroarenes were selectively converted into the corresponding secondary or tertiary amines in good to excellent yields without any co-catalysts, such as bases and stabilizing ligands. Copyright

Ruthenium-catalyzed tertiary amine formation from nitroarenes and alcohols

A highly selective ruthenium-catalyzed C-N bond formation was developed by using the hydrogen-borrowing strategy. Various tertiary amines were obtained efficiently from nitroarenes and primary alcohols. The reaction tolerates a wide range of functionalities. A tentative mechanism was proposed for this direct amination reaction of alcohols with nitroarenes.

Surfactant-assisted chromogenic sensing of cyanide in water

Chromogenic cyanide recognition in water was achieved by the use of a hydrophobic dye in micellar containers.

Ruthenium-catalysed selective N-monoalkylation of anilines with tetraalkyl-ammonium halides

Anilines react with an array of tetraalkylammonium halides in the presence of a catalytic amount of a ruthenium catalyst together with SnCl2·2H2O in dioxane at 180°C to afford selectively N-monoalkylanilines in good yields.