37529-29-6

Basic information

• Product Name: P-N-NONYLANILINE
• Synonyms: P-NONYLAMILINE;P-N-NONYLANILINE;4-Nonylaniline;4-n-Nonylaniline;p-Nonylaniline
• CAS NO: 37529-29-6
• Molecular Formula: C₁₅H₂₅N
• Molecular Weight: 219.37
• Product Categories: Alkyl;Alkylanilines
• Mol File: 37529-29-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 144/2mm
• Flash Point: >110°(230°F)
• Appearance: /
• Density: 0.913 g/cm³
• Vapor Pressure: 0.000138mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: P-N-NONYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: P-N-NONYLANILINE(37529-29-6)
• EPA Substance Registry System: P-N-NONYLANILINE(37529-29-6)

Safety Data

• Hazardous Substances Data: 37529-29-6(Hazardous Substances Data)

Usage

General Description

P-N-Nonylaniline is a synthetic, organic chemical compound that is part of the aniline family. Chemically, it is considered an aromatic amine, with the molecular formula written as C15H25N. This substance has the appearance of a brownish-powder or oily liquid. P-N-Nonylaniline is primarily used as an intermediate in the manufacturing of dyes and other chemical compounds. However, it is classified as hazardous and often harmful to humans and the environment. It can be toxic when ingested or absorbed through the skin, and has the potential to cause damage to the liver and kidneys.

InChI:InChI=1/C15H25N/c1-2-3-4-5-6-7-8-9-14-10-12-15(16)13-11-14/h10-13H,2-9,16H2,1H3

Upstream product

• 62-53-3 aniline 
• 143-08-8 nonyl alcohol 
• 124-11-8 non-1-ene 
• 764-85-2 Nonanoyl chloride 
• 1081-77-2 n-nonylbenzene 
• 17763-80-3 para-nitrophenyl triflate 
• 3088-78-6 dihydroxy-nonyl-borane 
• 71-43-2 benzene 
• 6008-36-2 1-phenylnonan-1-one 
• 80504-85-4 1-(4-nitrophenyl)-1,3-nonadiene 

Downstream Products

• 106132-85-8 (4-Nonyl-phenyl)-(4-propyl-phenyl)-diazene 
• 132329-29-4 4-Heptyloxy-benzoic acid 3-hydroxy-4-{[(E)-4-nonyl-phenylimino]-methyl}-phenyl ester 
• 132329-35-2 4-Octyloxy-benzoic acid 3-hydroxy-4-{[(E)-4-nonyl-phenylimino]-methyl}-phenyl ester 
• 126332-10-3 [1-(4-Butoxy-phenyl)-meth-(E)-ylidene]-(4-nonyl-phenyl)-amine 
• 1306630-52-3 C₅₀H₅₇N₅O₆ 
• 80155-20-0 4-(4-Nonyl-phenylazo)-phenol 
• 97586-30-6 5-Ethoxy-2-{[(E)-4-nonyl-phenylimino]-methyl}-phenol 
• 256383-45-6 (4-n-nonylphenyl)boronic acid 
• 1359844-16-8 C₁₅H₂₃I 
• 1356840-19-1 4-n-nonylbenzeneboronic acid pinacolate 
• 1349697-55-7 C₄₇H₆₂N₂O₂S₂ 

Relevant articles and documents

Design and synthesis of boronic acid inhibitors of endothelial lipase

Endothelial lipase (EL) and lipoprotein lipase (LPL) are homologous lipases that act on plasma lipoproteins. EL is predominantly a phospholipase and appears to be a key regulator of plasma HDL-C. LPL is mainly a triglyceride lipase regulating (V)LDL levels. The existing biological data indicate that inhibitors selective for EL over LPL should have anti-atherogenic activity, mainly through increasing plasma HDL-C levels. We report here the synthesis of alkyl, aryl, or acyl-substituted phenylboronic acids that inhibit EL. Many of the inhibitors evaluated proved to be nearly equally potent against both EL and LPL, but several exhibited moderate to good selectivity for EL.

Ring alkylation of aniline or an aniline derivative using ionic liquid catalysts

A process for ring-alkylating aniline or an aniline derivative in which aniline or an aniline derivative is reacted with an alkylating agent in the presence of an ionic liquid which includes a Lewis acid and a quaternary cation, to produce a ring-alkylated alkylaniline or a ring-alkylated aniline derivative. The use of an ionic liquid permits convenient separation of the alkylated reaction product from the reactants.

Method for preparing aromatic secondary amino compound

Disclosed are (1) a method for preparing an aromatic secondary amino compound which comprises reacting an N-cyclohexylideneamino compound in the presence of a hydrogen moving catalyst and a hydrogen acceptor by the use of a sulfur-free polar solvent and/or a cocatalyst, and (2) a method for preparing an aromatic secondary amino compound which comprises reacting cyclohexanone or a nucleus-substituted cyclohexanone, an amine and a nitro compound corresponding to the amine in a sulfur-free polar solvent in the presence of a hydrogen moving catalyst, a cocatalyst being added or not added.