4200-95-7

Basic information

• Product Name: 1-AMINOHEPTADECANE
• Synonyms: RARECHEM AL BW 0481;Aminoheptadecane;Heptadecylamin;1-AMINOHEPTADECANE 95+%;Heptadecane-1-amine;heptadecan-1-amine;1-heptadecanamine;Margarylamine
• CAS NO: 4200-95-7
• Molecular Formula: C₁₇H₃₇N
• Molecular Weight: 255.48
• EINECS: 224-103-7
• Product Categories: Alkylamines;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes
• Mol File: 4200-95-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 46 °C
• Boiling Point: 336 °C
• Flash Point: 146.2 °C
• Appearance: /
• Density: 0.8510
• Vapor Pressure: 0.000118mmHg at 25°C
• Refractive Index: 1.4510
• Solubility: soluble in Methanol
• PKA: 10.67±0.10(Predicted)
• CAS DataBase Reference: 1-AMINOHEPTADECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINOHEPTADECANE(4200-95-7)
• EPA Substance Registry System: 1-AMINOHEPTADECANE(4200-95-7)

Safety Data

• Hazardous Substances Data: 4200-95-7(Hazardous Substances Data)

Usage

General Description

1-Aminoheptadecane, also known as heptadecylamine, is a long-chain alkylamine compound with the chemical formula C17H37NH2. It is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. 1-Aminoheptadecane is primarily used as an intermediate in the production of surfactants, emulsifiers, corrosion inhibitors, and lubricants. It also finds application as a chemical precursor in the synthesis of pharmaceuticals, pesticides, and other organic compounds. Additionally, this chemical is utilized as a building block in the manufacture of cationic polymers, quaternary ammonium compounds, and other specialty chemicals. Overall, 1-Aminoheptadecane is a versatile compound with diverse industrial applications due to its long hydrophobic alkyl chain and amino functional group, making it useful in various chemical processes and products.

InChI:InChI=1/C17H37N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2-18H2,1H3

Upstream product

• 75-09-2 dichloromethane 
• 57-11-4 stearic acid 
• 110-54-3 hexane 
• 124-26-5 stearamide 
• 116557-12-1 eicosan-3-one oxime 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 629-73-2 1-Hexadecene 
• 201230-82-2 carbon monoxide 
• 100-46-9 benzylamine 
• 7418-01-1 heptadecyl isocyanate 
• 124-41-4 sodium methylate 
• 5399-02-0 heptadecanenitrile 
• 7418-04-4 heptadecyl-carbamic acid methyl ester 

Downstream Products

• 2524-46-1 sym-diheptadecylurea 
• 112152-91-7 sulfanilic acid heptadecylamide 
• 55775-34-3 N-heptadecyl(p-methoxy)aniline 
• 5638-17-5 N-heptadecylaniline 
• 1071160-14-9 C₃₄H₅₇N₃O₄S 
• 126145-75-3 C₁₀₃H₁₇₇N₃O₁₈ 

Relevant articles and documents

Observations on the Reaction of O-Acylthiohydroxamates with Thionitrite Esters: a Novel Free Radical Chain Reaction for Decarboxylative Amination

Treatment of primary and secondary O-acyl derivatives of N-hydroxy-2-thiopyridone with thionitrite esters gives trans nitroso dimers in a free radical chain reaction.

Sequential hydroaminomethylation/Pd-catalyzed hydrogenolysis as an atom efficient route to valuable primary and secondary amines

The facile synthesis of valuable primary and secondary amines is reported using a sequential procedure of hydroaminomethylation and Pd-catalyzed hydrogenolysis. The hydroaminomethylation reaction was catalyzed by a cationic Rh(I) iminopyridyl complex and the N-alkylated benzylamines were produced with high chemoselectivity, albeit as mixtures of linear and branched products. Performing the hydrogenolysis reaction using 10% Pd/C, provided access to valuable primary and secondary amines which have applications in the surfactant, pharmaceutical and polymer industries.

Selective Hydrogenation of Nitriles to Primary Amines by using a Cobalt Phosphine Catalyst

A general procedure for the catalytic hydrogenation of nitriles to primary amines by using a non-noble metal-based system is presented. Co(acac)3 in combination with tris[2-(dicyclohexylphosphino)ethyl]phosphine efficiently catalyzes the selective hydrogenation of a wide range of (hetero)aromatic and aliphatic nitriles to give the corresponding amines.