3065-46-1

Basic information

• Product Name: Ethanamine, 2,2-1,2-ethanediylbis(oxy)bisN,N-dimethyl-
• Synonyms: Ethanamine, 2,2-1,2-ethanediylbis(oxy)bisN,N-dimethyl-;1,2-Bis(2-dimethylaminoethoxy)ethane;N,N'-[Ethylenebis(oxyethylene)]bis(dimethylamine);2-[2-(2-dimethylaminoethyloxy)ethoxy]ethyl-dimethyl-amine;2-[2-(2-dimethylaminoethyloxy)ethoxy]-N,N-dimethylethanamine;2-[2-(2-dimethylaminoethyloxy)ethoxy]-N,N-dimethyl-ethanamine;2-[2-[2-(dimethylamino)ethoxy]ethoxy]-N,N-dimethylethanamine
• CAS NO: 3065-46-1
• Molecular Formula: C₁₀H₂₄N₂O₂
• Molecular Weight: 204.36
• Mol File: 3065-46-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 342.82°C (rough estimate)
• Flash Point: 64.3°C
• Appearance: /
• Density: 1.0048 (rough estimate)
• Refractive Index: 1.4610 (estimate)
• PKA: 9.10±0.28(Predicted)
• CAS DataBase Reference: Ethanamine, 2,2-1,2-ethanediylbis(oxy)bisN,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanamine, 2,2-1,2-ethanediylbis(oxy)bisN,N-dimethyl-(3065-46-1)
• EPA Substance Registry System: Ethanamine, 2,2-1,2-ethanediylbis(oxy)bisN,N-dimethyl-(3065-46-1)

Safety Data

• Hazardous Substances Data: 3065-46-1(Hazardous Substances Data)

Usage

Safety Profile

Moderately toxic by ingestion andskin contact. When heated to decomposition it emits toxicfumes such as NOx.

Upstream product

• 112-26-5 1,2-bis(2-chloroethoxy)ethane 
• 124-40-3 dimethyl amine 
• 31255-10-4 1,2-bis-(2-bromo-ethoxy)-ethane 
• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 

Downstream Products

• 109495-27-4 N,N'-diethyl-N,N,N',N'-tetramethyl-N,N'-(3,6-dioxa-octanediyl)-di-ammonium; diiodide 
• 58688-38-3 7,13-dimethyl-7,13-diaza-1,4,10-trioxacyclopentadecane 
• 31255-13-7 7,16-dimethyl-7,16-diaza-1,4,10,13-tetraoxacyclooctadecane 
• 72814-05-2 N,N-dimethyl-1,7,10,16-tetraoxa-4,13-diaza-(16)orthocyclophan 
• 108876-72-8 hexa-N-methyl-N,N'-(3,6-dioxa-octanediyl)-di-ammonium; diiodide 

Relevant articles and documents

Selective Synthesis of Bisdimethylamine Derivatives from Diols and an Aqueous Solution of Dimethylamine through Iridium-Catalyzed Borrowing Hydrogen Pathway

Bisdimethylamine derivatives are an important class of compounds in the polymer and pharmaceutical industries. However, existing methods for the synthesis of these compounds have several drawbacks such as low selectivity, use of toxic reagents, and generation of waste. In this study, a new system was developed for the selective synthesis of bisdimethylamine derivatives using a diol and dimethylamine as starting materials and an iridium complex bearing an N-heterocyclic carbene ligand as catalyst. The starting materials were easily available, less toxic, inexpensive, and easy to handle. The reaction proceeded efficiently through a borrowing hydrogen pathway under aqueous conditions, without any additional organic solvent, to afford various bisdimethylamine derivatives in good to excellent yields.