2044-21-5

Basic information

• Product Name: DI-N-NONYLAMINE
• Synonyms: 1-Nonanamine, N-nonyl-;1-nonanamine,N-nonyl-;N,N-bis(n-nonyl)amine;N,N-Dinonylamine;N-Nonyl-1-nonanamine;DINONYL-AMINE;DI-N-NONYLAMINE;N-nonylnonan-1-amine
• CAS NO: 2044-21-5
• Molecular Formula: C₁₈H₃₉N
• Molecular Weight: 269.51
• Product Categories: Aliphatics;Amines;Miscellaneous Reagents
• Mol File: 2044-21-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 24°C
• Boiling Point: 336°C
• Flash Point: 24 °C
• Appearance: /
• Density: 0.8055
• Vapor Pressure: 0.000107mmHg at 25°C
• Refractive Index: 1.4445
• CAS DataBase Reference: DI-N-NONYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: DI-N-NONYLAMINE(2044-21-5)
• EPA Substance Registry System: DI-N-NONYLAMINE(2044-21-5)

Safety Data

• Statements: 34
• Safety Statements: 26-36/37/39
• RIDADR: 2735
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 2044-21-5(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 2044-21-5 differently. You can refer to the following data:
1. Dinonylamine is an alkylamine that can be used in extraction of chloride complexes of niobium.
2. A alkylamine that can be used in extraction of chloride complexes of niobium.

InChI:InChI=1/C18H39N/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h19H,3-18H2,1-2H3

Upstream product

• 112-05-0 nonanoic acid 
• 100-61-8 N-methylaniline 

Downstream Products

• 86781-50-2 3-(2,4-Dimethyl-phenyl)-1,1-dinonyl-urea 
• 100-61-8 N-methylaniline 
• 2044-22-6 trinonyl-amine 

Relevant articles and documents

PRODUCTION OF AMINES

A process for the hydrogenation of carboxylic acids and/or derivatives, particularly amides, is described. The process includes reacting an acid or derivative such as an amide with a source of hydrogen in the presence of a catalyst system. The catalyst system obtainable by combining: (a) a source of ruthenium, and (b) a phosphine compound of general Formula I: (Formula I). The hydrogenation reaction is carried out in the presence of a low concentration of water or at low pressure or in the presence of a source of ammonia or the hydrogenation reaction is carried out in the absence of water or a combination of these factors is utilised. The invention also relates to the use of ammonia in the production of primary amines by hydrogenation of carboxylic acids and/or derivatives thereof or a process for the production of primary amines generally.