4200-95-7

Usage

Uses

Used in Surfactant Production:
1-Aminoheptadecane is used as an intermediate for the production of surfactants, which are essential in various industries for their ability to reduce surface tension and stabilize emulsions.
Used in Emulsifier Production:
1-Aminoheptadecane is used as an intermediate in the production of emulsifiers, which are crucial for creating stable mixtures of immiscible liquids, such as oil and water.
Used in Corrosion Inhibitor Production:
1-Aminoheptadecane is used as an intermediate in the synthesis of corrosion inhibitors, which are compounds that protect materials from corrosion by forming a protective film on their surface.
Used in Lubricant Production:
1-Aminoheptadecane is used as an intermediate in the production of lubricants, which are essential for reducing friction and wear in moving parts of machinery.
Used in Pharmaceutical Synthesis:
1-Aminoheptadecane is used as a chemical precursor in the synthesis of pharmaceuticals, where its unique structure can be utilized to create new and effective drug compounds.
Used in Pesticide Synthesis:
1-Aminoheptadecane is used as a chemical precursor in the synthesis of pesticides, where its properties can be leveraged to develop new and more effective pest control agents.
Used in Cationic Polymer Production:
1-Aminoheptadecane is used as a building block in the manufacture of cationic polymers, which have various applications in water treatment, paper production, and other industries.
Used in Quaternary Ammonium Compound Production:
1-Aminoheptadecane is used as a building block in the production of quaternary ammonium compounds, which are important in the formulation of disinfectants, sanitizers, and other antimicrobial agents.
Used in Specialty Chemicals Production:
1-Aminoheptadecane is utilized as a building block in the manufacture of specialty chemicals, where its unique properties can be tailored to meet specific industrial needs.

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

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

Downstream Products

• 89423-12-1 N-heptadecyl-phthalimide 
• 91472-69-4 N-heptadecyl-2,4,6-trinitroaniline 
• 126145-75-3 C₁₀₃H₁₇₇N₃O₁₈ 
• 1071160-14-9 C₃₄H₅₇N₃O₄S 
• 2524-46-1 sym-diheptadecylurea 
• 112152-91-7 sulfanilic acid heptadecylamide 
• 5638-17-5 N-heptadecylaniline 
• 55775-34-3 N-heptadecyl(p-methoxy)aniline 

Relevant academic research and scientific papers

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.

A State-of-the-Art Heterogeneous Catalyst for Efficient and General Nitrile Hydrogenation

Cobalt-doped hybrid materials consisting of metal oxides and carbon derived from chitin were prepared, characterized and tested for industrially relevant nitrile hydrogenations. The optimal catalyst supported onto MgO showed, after pyrolysis at 700 °C, magnesium oxide nanocubes decorated with carbon-enveloped Co nanoparticles. This special structure allows for the selective hydrogenation of diverse and demanding nitriles to the corresponding primary amines under mild conditions (e.g. 70 °C, 20 bar H2). The advantage of this novel catalytic material is showcased for industrially important substrates, including adipodinitrile, picolinonitrile, and fatty acid nitriles. Notably, the developed system outperformed all other tested commercial catalysts, for example, Raney Nickel and even noble-metal-based systems in these transformations.

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.

The reaction of thionitrites with Barton esters: A convenient free radical chain reaction for decarboxylative nitrosation

Tertiary thionitrite esters react with primary and secondary O-acyl derivatives of N-hydroxy-2-thiopyridone to give trans nitroso dimers as the principal products of a free radical chain reaction.