4746-32-1

Basic information

• Product Name: N-HEXYLANILINE, 98%
• Synonyms: N-n-Hexylaniline, 98%
• CAS NO: 4746-32-1
• Molecular Formula: C₁₂H₁₉N
• Molecular Weight: 177.29
• Product Categories: Amines;C11 to C38;Nitrogen Compounds
• Mol File: 4746-32-1.mol
• Article Data: 141

Chemical Properties

• Boiling Point: 140-145 °C/15 mmHg
• Flash Point: 110 °C
• Appearance: Colorless to brown/Liquid
• Density: 0.8994 g/mL at 25 °C
• Vapor Pressure: 0.0049mmHg at 25°C
• Refractive Index: n20/D 1.5228
• PKA: 5.05±0.50(Predicted)
• CAS DataBase Reference: N-HEXYLANILINE, 98%(CAS DataBase Reference)
• NIST Chemistry Reference: N-HEXYLANILINE, 98%(4746-32-1)
• EPA Substance Registry System: N-HEXYLANILINE, 98%(4746-32-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 4746-32-1(Hazardous Substances Data)

Usage

Description

N-HEXYLANILINE, 98% is a chemical compound with a purity of 98%, belonging to the class of aniline organic compounds derived from benzene. It is specifically composed of a hexyl group attached to the amine functional group, known for its strong odor and versatile industrial applications.

Uses

Used in Chemical Production:
N-HEXYLANILINE, 98% is used as an intermediate in the production of dyes, pigments, and other organic compounds, contributing to the coloration and enhancement of various products.
Used in Textile Industry:
In the textile industry, N-HEXYLANILINE, 98% is utilized for dyeing and finishing processes, providing color and improving the quality of fabrics.
Used in Plastics and Rubber Manufacturing:
This chemical compound is employed in the manufacturing of plastics and rubber, where it serves to modify properties such as flexibility, durability, and color.
Used as a Catalyst in Chemical Reactions:
N-HEXYLANILINE, 98% is used as a catalyst to facilitate various chemical reactions, enhancing the efficiency and speed of these processes.
Used in Metalworking Processes:
As a corrosion inhibitor, N-HEXYLANILINE, 98% is applied in metalworking processes to protect metals from corrosion, ensuring the longevity and integrity of metal components.

InChI:InChI=1/C12H19N/c1-2-3-4-8-11-13-12-9-6-5-7-10-12/h5-7,9-10,13H,2-4,8,11H2,1H3

Upstream product

• 638-45-9 1-Iodohexane 
• 62-53-3 aniline 
• 544-10-5 1-Chlorohexane 
• 111-25-1 1-bromo-hexane 
• 111-27-3 hexan-1-ol 
• 103-70-8 Formanilid 
• 108-86-1 bromobenzene 
• 111-26-2 hexan-1-amine 
• 66-25-1 hexanal 
• 98-95-3 nitrobenzene 
• 1483-73-4 diphenyliodonium bromide 
• 591-50-4 iodobenzene 
• 108-90-7 chlorobenzene 
• 21369-64-2 n-hexyllithium 

Downstream Products

• 37877-50-2 N-hexyl-toluene-4-sulfonanilide 
• 50917-04-9 chloro-acetic acid-(N-hexyl-anilide) 
• 55239-83-3 C₁₃H₁₈ClNO 
• 83715-94-0 10-Hexyl-3-phenyl-10H-pyrimido[4,5-b]quinoline-2,4-dione 
• 213190-21-7 Hexyl-phenyl-dithiocarbamic acid methyl ester 
• 33228-45-4 4-hexylaniline 
• 62-53-3 aniline 
• 66-25-1 hexanal 
• 20330-59-0 N-(4-hexylphenyl)acetamide 
• 32416-69-6 N-hexyl-4-nitroso-aniline 
• 1263079-29-3 C₄₅H₆₃N₃ 
• 1202804-81-6 C₃₂H₄₄N₂ 
• 1202804-72-5 C₃₂H₄₄N₂ 
• 72450-68-1 N-benzyl-N-hexyl aniline 

Relevant articles and documents

Mechanistic Analysis of Metallaphotoredox C-N Coupling: Photocatalysis Initiates and Perpetuates Ni(I)/Ni(III) Coupling Activity

The combined use of reaction kinetic analysis, ultrafast spectroscopy, and stoichiometric organometallic studies has enabled the elucidation of the mechanistic underpinnings to a photocatalytic C-N cross-coupling reaction. Steady-state and ultrafast spect

Solvent-dependent nuclearity, geometry and catalytic activity of [(SPhos)Pd(Ph)Cl]2

The nuclearity and structures of the palladium complex [(SPhos)Pd(Ph)Cl]2 in the solid and solution states are revisited using a combination of Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy, NMR spectroscopy, mass spectrometry,

Reductive amination of ketones/aldehydes with amines using BH3N(C2H5)3as a reductant

Herein, we report the first example of efficient reductive amination of ketones/aldehydes with amines using BH3N(C2H5)3 as a catalyst and a reductant under mild conditions, affording various tertiary and secondary amines in excellent yields. A mechanistic study indicates that BH3N(C2H5)3 plays a dual function role of promoting imine and iminium formation and serving as a reductant in reductive amination. This journal is

Ligand compound for copper catalyzed aryl halide coupling reaction, catalytic system and coupling reaction

The invention provides a ligand compound capable of being used for copper catalyzed aryl halide coupling reaction, the ligand compound is a three-class compound containing a 2-(substituted or non-substituted) aminopyridine nitrogen-oxygen group, and the invention also provides a catalytic system for the aryl halide coupling reaction. Thecatalytic system comprises a copper catalyst, a compound containing a 2-(substituted or non-substituted) aminopyridine nitrogen-oxygen group adopted as a ligand, alkali and a solvent, and meanwhile, the invention also provides a system for the aryl halide coupling reaction adopting the catalyst system. The compound containing the 2-(substituted or non-substituted) aminopyridine nitrogen oxygen group can be used as the ligand for the copper catalyzed aryl chloride coupling reaction, and the ligand is stable under a strong alkaline condition and can well maintain catalytic activity when being used for the copper-catalyzed aryl chloride coupling reaction. In addition, the copper catalyst adopting the compound as the ligand can particularly effectively promote coupling of copper catalyzed aryl chloride and various nucleophilic reagents which are difficult to generate under conventional conditions, C-N, C-O and C-S bonds are generated, and numerous useful small molecule compounds are synthesized. Therefore, the aryl halide coupling reaction has a very good large-scale application prospect by adopting the copper catalysis system of the ligand.