4013-95-0

Basic information

• Product Name: N,N'-dibutylethylenediamine
• Synonyms: N,N'-Dibutylethane-1,2-diamine;butyl-[2-(butylamino)ethyl]amine;N1,N2-dibutylethane-1,2-diamine
• CAS NO: 4013-95-0
• Molecular Formula: C10H24N2
• Molecular Weight: 172.32
• EINECS: 223-667-1
• Mol File: 4013-95-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N'-dibutylethylenediamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-dibutylethylenediamine(4013-95-0)
• EPA Substance Registry System: N,N'-dibutylethylenediamine(4013-95-0)

Safety Data

• Hazardous Substances Data: 4013-95-0(Hazardous Substances Data)

Upstream product

• 534-26-9 lysidine 
• 109-65-9 1-bromo-butane 
• 925-49-5 N,N'-ethanediyl-bis-butyramide 
• 107-06-2 1,2-dichloro-ethane 
• 109-73-9 N-butylamine 
• 106-93-4 ethylene dibromide 
• 123-72-8 butyraldehyde 
• 107-15-3 ethylenediamine 
• 71-36-3 butan-1-ol 
• 50-99-7 D-glucose 
• 56-81-5 glycerol 
• 7020-84-0 N,N'-di(butylidene)ethylenediamine 
• 14040-75-6 N,N'-bis(n-butyl)oxamide 

Downstream Products

• 73941-39-6 1,3-dibutyl-2-propyl-imidazolidine 
• 4761-09-5 1,3-Dibutyl-imidazolidin-2-on 
• 97863-91-7 1,3-dibutyl-2-phenyl-[1,3,2]diazaborolidine 
• 56270-03-2 1,3-dibutyl-2-methyl-2-phenyl-[1,3,2]diazasilolidine 
• 124-40-3 dimethyl amine 

Relevant articles and documents

Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis

Short amines, such as ethanolamines and ethylenediamines, are important compounds in today's bulk and fine chemicals industry. Unfortunately, current industrial manufacture of these chemicals relies on fossil resources and requires rigorous safety measures when handling explosive or toxic intermediates. Inspired by the elegant working mechanism of aldolase enzymes, a novel heterogeneously catalyzed process—reductive aminolysis—was developed for the efficient production of short amines from carbohydrates at low temperature. High-value bio-based amines containing a bio-derived C2 carbon backbone were synthesized in one step with yields up to 87 C%, in the absence of a solvent and at a temperature below 405 K. A wide variety of available primary and secondary alkyl- and alkanolamines can be reacted with the carbohydrate to form the corresponding C2-diamine. The presented reductive aminolysis is therefore a promising strategy for sustainable synthesis of short, acyclic, bio-based amines.

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.

Method and apparatus for sunless tanning

Apparatus for simulating skin tanning comprises a receptacle containing a fluid comprising dihydroxyacetone, a receptacle containing a fluid comprising a secondary polyamine, and dispensing means for simultaneously or sequentially providing desired amounts of dihydroxyacetone and polyamine.