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18408-42-9

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18408-42-9 Usage

General Description

Bis(trimethylsilyl)sebacate, also known as decanedioic acid bis(trimethylsilyl) ester, is a chemical compound with the molecular formula C18H38O4Si2. The compound belongs to the organic silicons category and is derived from sebacic acid and trimethylsilane. It's a colorless liquid and is widely used in industrial applications such as the production of adhesives, sealants, and lubricants. It is also a processing aid in the manufacture of rubber products. Despite its industrial significance, there is a lack of data about its environmental and human health impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 18408-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18408-42:
(7*1)+(6*8)+(5*4)+(4*0)+(3*8)+(2*4)+(1*2)=109
109 % 10 = 9
So 18408-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H34O4Si2/c1-21(2,3)19-15(17)13-11-9-7-8-10-12-14-16(18)20-22(4,5)6/h7-14H2,1-6H3

18408-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis(trimethylsilyl)decanedioate

1.2 Other means of identification

Product number -
Other names Decandisaeure-bis-trimethylsilylester

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:18408-42-9 SDS

18408-42-9Downstream Products

18408-42-9Relevant articles and documents

-

Henglein et al.

, p. 1,21, 22 (1957)

-

Dealkylation of esters via treatment with N-(trimethylsilyl) diethylamine and methyl iodide

Yamamoto, Yasushi,Shimizu, Hideaki,Hamada, Yoshitaka

, p. 119 - 122 (2007/10/03)

A method for the conversion of esters to carboxylic acids has been reported. Reaction of methyl o-methoxybenzoate with N-(trimethylsilyl)diethylamine and methyl iodide, followed by hydrolysis, afforded o-methoxybenzoic acid with a 94% yield based on 96% conversion. Methyl esters of not only aromatic acids but also aliphatic acids were converted to the corresponding acids with high yields. A combination of N-(trimethylsilyl)dimethylamine and methyl iodide was also effective to give p-methylbenzoic acid with a 85% yield based on 90% conversion from the corresponding methyl ester.

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