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1836-42-6

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1836-42-6 Usage

General Description

Benzyltriethylammonium hydroxide is a quaternary ammonium hydroxide used as a strong base in various chemical reactions and processes. It is commonly used in organic synthesis as a catalyst for the formation of carbon-carbon and carbon-heteroatom bonds. This chemical compound is also utilized in the manufacturing of pharmaceuticals, dyes, and surfactants. Due to its highly basic nature, it must be handled with care and stored properly to prevent accidental exposure and potential hazards. Benzyltriethylammonium hydroxide is an important reagent in the field of organic chemistry and is widely utilized in industrial and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1836-42-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1836-42:
(6*1)+(5*8)+(4*3)+(3*6)+(2*4)+(1*2)=86
86 % 10 = 6
So 1836-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H22N.H2O/c1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;/h7-11H,4-6,12H2,1-3H3;1H2/q+1;/p-1

1836-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl(triethyl)azanium,hydroxide

1.2 Other means of identification

Product number -
Other names triethylbenzylammonium hydroxyde

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:1836-42-6 SDS

1836-42-6Relevant articles and documents

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.

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