13093-05-5

Usage

Uses

Used in Polymer Industry:
N,N'-Diethyl-1,6-diaminohexane is used as a cross-linking agent for enhancing the properties of polymers. Its ability to cause cross-linking between polymer chains results in improved strength, durability, and stability of the final polymer products.
Used in Chemical Catalysts:
N,N'-Diethyl-1,6-diaminohexane is used as a catalyst in various chemical reactions due to its amine groups. These groups facilitate the progress of reactions, making it an essential component in certain industrial processes.

Upstream product

• 629-03-8 1 ,6-dibromohexane 
• 75-04-7 ethylamine 
• 124-09-4 1,6-Hexanediamine 
• 75-07-0 acetaldehyde 
• 3073-59-4 hexamethylene bisacetamide 
• 64-17-5 ethanol 
• 638132-53-3 (Z)-1-{N-ethyl-N-[6-(N-ethylammoniohexyl)amino]}diazen-1-ium-1,2-diolate 
• 102550-53-8 N,N'-diethyl-N,N'-hexanediyl-bis-benzenesulfonamide 

Downstream Products

• 81942-58-7 1,6-bis-(1-ethyl-3-phenylureido-1-yl)hexane 
• 3613-89-6 1,6-Bis-(ethyl-dichloracetyl-amino)-hexan 

Relevant academic research and scientific papers

Synthesis of N,N′-disubstituted α,ω-alkanediamines, precursors of linear bis dithiocarbamates

Linear bis dithiocarbamates are conveniently obtained from symmetrical disubstituted α,ω-alkanediamines whose preparation is reported.

Use of additive sites to control nitric oxide release from nitric oxide donors contained within polymers

A method for increasing, prolonging, and/or controlling the release rates of nitric oxide (NO) from polymeric materials containing NO adducts. Such NO-containing polymeric materials may find use in devices such as blood contacting devices, and biocompatible devices utilizing the same. The method and device utilizes anionic site additives, acidic site additives and/or acidic producing site additives in a polymer that contains NO-adducts to generate higher fluxes of NO to exceed NO threshold levels desirable to substantially prevent and/or minimize reactions such as platelet activation or adhesion.

METHOD FOR PRODUCING N-MONOALKYL-SUBSTITUTED ALKYLENE AMINE

PROBLEM TO BE SOLVED: To provide a method for producing an N-monoalkyl-substituted alkylene amine especially useful for uses such as medicine intermediates, agrochemical intermediates, urethane resin-foaming catalysts, surfactants and the like among alkyl-substituted alkylene amine compounds from an alcohol and an alkylene amine as raw materials. SOLUTION: This method for producing the N-monoalkyl-substituted alkylene amine is characterized by reacting the alkylene amine with a ≥2C alkyl alcohol in the presence of a copper-containing oxide catalyst system. The N-monoalkyl-substituted alkylenamine is produced in high conversion and in N-monoalkylation selectivity.

N-(2-METHYL-2-NITROPROPYL) AND N-NITROSO DERIVATIVES OF SOME DIAMINES

Preparation of ten new derivatives of 1,6-hexanediamine and 1,4-bis(4-aminophenoxy)butane with different combination of N-nitroso and/or N-(2-methyl-2-nitropropyl) groups is presented.The title compounds are potential improvers of vulcanized rubber dynamic properties.

Novel polytriazine compounds

Novel tetraalkyl piperidine radical containing polytriazine compounds are produced by reacting a dihalogen-triazine with a bifunctional compound containing amine, alcohol, mercaptan or phenol groups at least one of the bifunctional compounds containing a tetraalkyl piperidine radical. The compounds are valuable light stabilizers for synthetic polymers, particularly polyolefin in the form of fibers or films.