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Benzenemethanaminium, N,N,N-triethyl-, ethoxide, also known as triethylamine ethoxide, is an organic compound with the chemical formula C11H20NO. It is formed by the reaction of triethylamine (a tertiary amine) with ethanol, resulting in a quaternary ammonium salt. Benzenemethanaminium, N,N,N-triethyl-, ethoxide is widely used as a phase-transfer catalyst in various organic synthesis reactions, particularly in the preparation of esters, amides, and other organic compounds. Triethylamine ethoxide is known for its ability to facilitate the transfer of reactants between immiscible phases, such as between an aqueous and an organic phase, thereby enhancing the efficiency of the reaction. It is also used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle Benzenemethanaminium, N,N,N-triethyl-, ethoxide with care, following proper safety protocols.

95903-96-1

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95903-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95903-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,9,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95903-96:
(7*9)+(6*5)+(5*9)+(4*0)+(3*3)+(2*9)+(1*6)=171
171 % 10 = 1
So 95903-96-1 is a valid CAS Registry Number.

95903-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triethylbenzylammonium ethanolate

1.2 Other means of identification

Product number -
Other names triethylbenzylammonium ethoxide

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:95903-96-1 SDS

95903-96-1Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF TRIETHYLBENZYLAMMONIUM ALKOXIDES. REACTIVITY IN ELIMINATION AND NUCLEOPHILIC SUBSTITUTION REACTIONS

Shavanov, S. S.,Tolstikov, G. A.,Shutenkova, T. V.,Ryabova, N. A.,Filippova, S. A.

, p. 643 - 647 (2007/10/02)

Triethylbenzylammonium alkoxides exhibit high reactivity during the elimination of hydrogen chloride from polychloroalkanes and can also be used in the synthesis of ethers from halogenoalkanes.Quaternary ammonium salts do not form tetraalkylammonium or trialkylbenzylammonium alkoxides under the influence of a concentrated aqueous solution of sodium hydroxide in the presence of alcohols.

CATALYSIS OF LIQUID-PHASE DEHYDROCHLORINATION OF 1,1,2-TRICHLOROETHANE.

Shavanov,Tolstikov,Viktorov,Shutenkova

, p. 139 - 141 (2007/10/02)

Experiments show that vinylidene chloride can be obtained in virtually quantitative yield by the use of triethylbenzylammonium alkoxides as catalysts of 1,1,2-trichloroethane dehydrochlorination. Catalyst anions containing an unsaturated carbon bond in the position relative to oxygen increase catalyst activity. The catalyst is present in the organic phase and is not transferred from one phase into the other.

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