7403-68-1

Basic information

• Product Name: 2-[(2,2-dimethylpropyl)amino]ethanol
• Synonyms: 2-(neopentylamino)ethanol
• CAS NO: 7403-68-1
• Molecular Formula: C₇H₁₇NO
• Molecular Weight: 131.216
• Mol File: 7403-68-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 204.8°C at 760 mmHg
• Flash Point: 66.5°C
• Density: 0.872g/cm³
• Vapor Pressure: 0.062mmHg at 25°C
• Refractive Index: 1.439
• CAS DataBase Reference: 2-[(2,2-dimethylpropyl)amino]ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2,2-dimethylpropyl)amino]ethanol(7403-68-1)
• EPA Substance Registry System: 2-[(2,2-dimethylpropyl)amino]ethanol(7403-68-1)

Safety Data

• Hazardous Substances Data: 7403-68-1(Hazardous Substances Data)

Usage

General Description

2-[(2,2-dimethylpropyl)amino]ethanol, also known as DMPO, is a chemical compound with the molecular formula C7H17NO. It is an amino alcohol, which means it contains both an amine and an alcohol functional group. DMPO is often used as a catalyst in organic synthesis reactions and as a stabilizer in pharmaceuticals and personal care products. It is a colorless liquid with a slightly ammoniacal odor and is soluble in water, alcohols, and ethers. DMPO is considered to be relatively low in toxicity, but it should still be handled with care and proper protective equipment.

Upstream product

• 75-84-3 2,2-dimethyl-propanol-1 
• 141-43-5 ethanolamine 
• 75-21-8 oxirane 
• 5813-64-9 2.2-dimethylpropylamine 
• 630-19-3 pivalaldehyde 

Relevant articles and documents

N-Alkylation of Alkylolamines with Alcohols Over Mesoporous Solid Acid–Base Cs–B–Zr Catalyst

Abstract: The mesoporous solid acid–base Cs–B–Zr mixed oxides were synthesized using the co-precipitation method followed by a subsequent thermal treatment. The catalytic activity of solid Cs–B–Zr mixed oxide was tested for solvent free acid–base catalysed direct alkylolamines with alcohols as green alkylating agent. The effects of Cs/B/Zr ratio, calcination temperature, reaction conditions, and reaction substrate on the catalytic performance of the catalysts were investigated. The XRD, N2 adsorption–desorption, ICP-OES, FT-IR and NH3/CO2-TPD results showed that the mesoporous structure and acid–base properties of the catalysts play important roles in the reaction. A suitable number of acid and basic sites on the catalyst lead to a high activity for the N-alkylation reaction. Graphical Abstract: A direct N-alkylation of amino alcohol with alcohols has been developed using mixed oxide Cs–B–Zr as an acid–base bifunctionalized catalyst.[Figure not available: see fulltext.]

Method of producing optically active, 4-substituted (S)-2-oxazolidinones

The invention relates to a method of producing optically active, 4-substituted (S)-2-Oxazolidinones, novel (S)-2-oxazolidinones, novel, optically active (S)-amino alcohols and the use of these compounds.