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2-[(2,2-dimethylpropyl)amino]ethanol, also known as 2-(2,2-dimethylpropylamino)ethanol, is an organic compound with the chemical formula C7H17NO. It is a colorless liquid with a molecular weight of 129.22 g/mol. 2-[(2,2-dimethylpropyl)amino]ethanol is characterized by the presence of a primary amine group attached to a 2,2-dimethylpropyl chain and an ethanol group. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its amine functionality, it can participate in a range of chemical reactions, such as acylation, alkylation, and condensation, making it a versatile building block in organic synthesis.

7403-68-1

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7403-68-1 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.

Check Digit Verification of cas no

The CAS Registry Mumber 7403-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7403-68:
(6*7)+(5*4)+(4*0)+(3*3)+(2*6)+(1*8)=91
91 % 10 = 1
So 7403-68-1 is a valid CAS Registry Number.

7403-68-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,2-dimethylpropylamino)ethanol

1.2 Other means of identification

Product number -
Other names 2-neopentylamino-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7403-68-1 SDS

7403-68-1Downstream Products

7403-68-1Relevant academic research and scientific papers

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

Chen, Aimin,Wang, Houyong,Liu, Rui,Bo, Yingying,Hu, Jun

, p. 1182 - 1193 (2016/07/06)

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.]

PHOSPHONOOXY QUINAZOLINE DERIVATIVES AND THEIR PHARMACEUTICAL USE

-

Page 82, (2008/06/13)

Quinazoline derivatives of formula (I) wherein A is 5-membered heteroaryl containing a nitrogen atom and one or two further nitrogen atoms; compositions containing them, processes for their preparation and their use in therapy.

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

-

, (2008/06/13)

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.

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