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Usage

Uses

Used in Pharmaceutical Industry:
2-Aminoundecane is used as a chemical intermediate for the synthesis of pharmaceuticals. Its role in this industry is crucial as it aids in the production of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Surfactant Production:
In the manufacturing of surfactants, 2-Aminoundecane is utilized as a key component. Surfactants are essential in a wide range of products, from detergents to cosmetics, due to their ability to reduce surface tension and stabilize mixtures.
Used in Laboratory Chemicals:
2-Aminoundecane is also used in the production of laboratory chemicals. It is an important reagent in various chemical reactions and research processes, facilitating scientific investigations and experiments.
Used as a Reagent in Chemical Reactions:
2-AMINOUNDECANE functions as a reagent in a variety of chemical reactions, playing a significant role in the synthesis of complex organic molecules and contributing to the advancement of chemical research and development.

InChI:InChI=1/C11H25N/c1-3-4-5-6-7-8-9-10-11(2)12/h11H,3-10,12H2,1-2H3

Upstream product

• 2158-28-3 undecan-2-one oxime 
• 112-12-9 methyl nonyl ketone 
• 78527-33-0 N-(1-methyl-decyl)-formamide 
• 123-91-1 1,4-dioxane 

Relevant academic research and scientific papers

Selective synthesis of primary amines by reductive amination of ketones with ammonia over supported Pt catalysts

Supported platinum catalysts are studied for the reductive amination of ketones under ammonia and hydrogen. For a model reaction with 2-adamantanone, Pt-loaded MoOx/TiO2 (Pt-MoOx/TiO2) shows the highest yield of primary amine. The catalyst is effective for the selective transformation of various aliphatic and aromatic ketones to the corresponding primary amines, which demonstrates the first example of the selective synthesis of primary amines by this reaction. The yield of the amine increases with increase in the negative shift of the C￡O stretching band in the infrared spectra of adsorbed acetone on the catalysts, suggesting that Lewis acid sites on the support material play an important role in this catalytic system.

Selective reductions. Part 60: Chemoselective reduction of organyl azides with dichloroborane-dimethyl sulfide

The rate and stoichiometry of the reduction of an organyl azide with BH3·THF was examined under standardized conditions at room temperature. Borane derivatives, such as dialkyl-, alkoxy-, and haloboranes were also examined for the reduction of azides. This study revealed BHCl2·SMe2 to be the most suitable reagent for the reduction of azides. The chemoselectivity of this reagent was also studied by reducing n-hexyl azide in the presence of representative series of functional groups, including esters, halides, nitriles, and nitro groups. BHCl2·SMe2 reduces azides in the presence of all of the above functional groups as well as olefins. Taking advantage of the differences in reactivity of BHCl2·SMe2 and BH3·THF or BH3·SMe2, it is now possible to reduce selectively an azide in the presence of olefins or to hydroborate an olefin in the presence of azides by a judicious choice of the reagent.

DICHLOROBORANE-DIMETHYL SULFIDE, A HIGHLY SELECTIVE REDUCING AGENT FOR REDUCTION OF ORGANYL AZIDES TO AMINES

Dichloroborane-dimethylsulfide reduces a variety of organyl azides, such as primary, secondary, tertiary, and aromatic to the corresponding amines in excellent yields.Cycloalkyl and benzylic azides are also readily reduced by this reagent.The reduction of azide with BHCl2*SMe2 is highly selective and many functional groups, such as halogen, ester, nitrile, aliphatic and armatic nitro, survice in this process.