3529-09-7

Basic information

• Product Name: N,N-DI-N-BUTYLETHYLENEDIAMINE
• Synonyms: 1,2-Ethanediamine, N,N-dibutyl-;2-DI-N-BUTYLAMINOETHYLAMINE;N,N-DI-N-BUTYLETHYLENEDIAMINE;TIMTEC-BB SBB005880;Dibutylethylenediamine;N,N-Di-n-butylethylenediamine,98%;2-(dibutylamino)ethylamine;N,N-Dibutyl-1,2-ethanediamine
• CAS NO: 3529-09-7
• Molecular Formula: C₁₀H₂₄N₂
• Molecular Weight: 172.31
• EINECS: 222-558-6
• Mol File: 3529-09-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 187-188 °C
• Boiling Point: 109-114°C 20mm
• Flash Point: 88°C
• Appearance: /
• Density: 0,82 g/cm3
• Vapor Pressure: 0.125mmHg at 25°C
• Refractive Index: 1.4430
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 9.67±0.10(Predicted)
• BRN: 1738440
• CAS DataBase Reference: N,N-DI-N-BUTYLETHYLENEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DI-N-BUTYLETHYLENEDIAMINE(3529-09-7)
• EPA Substance Registry System: N,N-DI-N-BUTYLETHYLENEDIAMINE(3529-09-7)

Safety Data

• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: 2735
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 3529-09-7(Hazardous Substances Data)

Usage

Description

N,N-Di-N-butylethylenediamine, also known as N,N-Dibutylethane-1,2-diamine, is an organic compound with the chemical formula C10H22N2. It is characterized by its amine functional groups and butyl substituents, which contribute to its unique properties and applications.

Uses

Used in Flavor Industry:
N,N-Di-N-butylethylenediamine is used as a volatile flavor compound in the food industry, specifically for enhancing the taste and aroma of semi-wild-blood Aba Tibetan pork. Its unique chemical structure allows it to contribute to the distinct flavor profile of this particular type of meat, making it a valuable additive in the culinary world.
Please note that the provided materials only mention the use of N,N-Di-N-butylethylenediamine as a flavor compound in the food industry. If there are other applications in different industries, they are not mentioned in the provided materials.

InChI:InChI=1/C10H24N2/c1-3-5-8-12(10-7-11)9-6-4-2/h3-11H2,1-2H3

Upstream product

• 111-92-2 dibutylamine 
• 107-15-3 ethylenediamine 
• 71-36-3 butan-1-ol 
• 82154-67-4 N-(2-(Dibutylamino)ethyl)propionamide 
• 18071-38-0 N,N-dibutyl-glycine nitrile 
• 151-56-4 ethyleneimine 
• 6287-40-7 dibutylamine hydrochloride 

Downstream Products

• 56224-59-0 N,N'-Bis-(2-dibutylamino-ethyl)-4,6-dinitro-benzene-1,3-diamine 
• 422524-37-6 N'-(4-benzyloxy-benzyl)-N,N-dibutyl-ethane-1,2-diamine 
• 23445-47-8 4.4'-Dimethyl-benzilsaeure-N-(β-dibutyl-amino-ethyl)-amid 
• 23445-49-0 4.4'-Difluor-benzilsaeure-N-<β-dibutylamino-ethyl>-amid 
• 31416-51-0 4.4'-Dichlor-benzilsaeure-N-(β-dibutyl-amino-ethyl)-amid 
• 23445-57-0 4.4'-Dibrom-benzilsaeure-N-(β-dibutyl-amino-ethyl)-amid 
• 23437-40-3 Benzilsaeure-N-<β-dibutylamino-ethyl>-amid 
• 23437-42-5 3.3'-Dimethyl-benzilsaeure-N-(β-dibutyl-amino-ethyl)-amid 
• 23445-51-4 3.3'-Dichlor-benzilsaeure-N-(β-dibutyl-amino-ethyl)-amid 
• 23445-48-9 4,4'-Dimethoxybenzilsaeure-N-(β-dibutylaminoethyl)-amid 
• 23445-50-3 2.2'-Dichlor-benzilsaeure-N-<β-dibutyl-amino-ethyl>-amid 
• 23536-29-0 2,2'-Dimethoxybenzilsaeure-N-(β-dibutylaminoethyl)-amid 
• 223651-67-0 [2-[[N-[2-(Dibutylamino)ethyl]carbamoyloxy]methyl]phenyl]-N-octadecylformamide 
• 1393827-99-0 3,4-diphenyl-1H-pyrrole-2,5-dicarboxylic acid bis[(2-dibutylaminoethyl)amide] 

Relevant articles and documents

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.

Some new derivatives of phenoxyacetic acid

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