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2-(2-hydroxyethyl-(1-phenylethyl)amino)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

46407-94-7

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46407-94-7 Usage

General Description

2-(2-hydroxyethyl-(1-phenylethyl)amino)ethanol, or N-(2-hydroxy-ethyl)-N-phenethylethanolamine, is a synthetic chemical compound that belongs to the class of amine compounds. It is a colorless liquid with a slightly fishy odor, and is often used as a chelating agent in metalworking and textile industry, as well as a component in some industrial and commercial cleaning products. It also has applications in the production of cosmetics and personal care products, where it can act as a surfactant, emulsifier, and conditioning agent. However,

Check Digit Verification of cas no

The CAS Registry Mumber 46407-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,4,0 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 46407-94:
(7*4)+(6*6)+(5*4)+(4*0)+(3*7)+(2*9)+(1*4)=127
127 % 10 = 7
So 46407-94-7 is a valid CAS Registry Number.

46407-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-hydroxyethyl(1-phenylethyl)amino]ethanol

1.2 Other means of identification

Product number -
Other names -

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:46407-94-7 SDS

46407-94-7Downstream Products

46407-94-7Relevant academic research and scientific papers

Enhanced asymmetric induction in cycloadditions to bridgehead-chiral vinyl dioxazaborocines

Davies, Christopher D.,Marsden, Stephen P.,Stokes, Elaine S.E.

, p. 4229 - 4233 (2000)

Vinyl dioxazaborocines 5 with asymmetric centres on the nitrogen bridgehead substituent have been prepared and assayed in nitrile oxide and nitrone cycloadditions, giving asymmetric inductions of up to 70 and 74% ee, respectively. (C) 2000 Elsevier Science Ltd.

ASYMMETRIC REDUCTION OF KETONES USING LiAlH4 MODIFIED WITH CHIRAL 1,2-AMINODIOLS

Morrison, James D.,Grandbois, Edward R.,Howard, Sachiko I.,Weisman, Gary R.

, p. 2619 - 2622 (2007/10/02)

Four chiral aminodiols from ring opening of (S)-propylene oxide and ethylene oxide with n-butylamine and (R) or (S)-α-methylbenzylamine were used to modify LiAlH4.Asymmetric reduction of acetophenone and propiophenone gave the highest percent enantiomeric

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