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6221-88-1

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6221-88-1 Usage

Description

(dodecyloxy)(trimethyl)silane is a chemical compound that belongs to the class of organosilicon compounds, characterized by its molecular formula C18H40OSi and a molecular weight of 300.69 g/mol. It is known for its versatile applications in modifying surface properties and enhancing the performance characteristics of various materials.

Uses

Used in Surface Modification:
(dodecyloxy)(trimethyl)silane is used as a surface modifier to alter the properties of materials, such as improving their hydrophobicity, adhesion, and resistance to environmental factors.
Used in Silicon-Containing Material Synthesis:
In the chemical industry, (dodecyloxy)(trimethyl)silane is used as a key component in the synthesis of various silicon-containing materials, contributing to the development of new products with unique properties.
Used as a Coupling Agent:
(dodecyloxy)(trimethyl)silane serves as a coupling agent, facilitating the bonding between different materials and enhancing the overall performance of formulations such as coatings, adhesives, and sealants.
Used as an Adhesion Promoter:
It is also utilized as an adhesion promoter to improve the bonding strength between different materials, ensuring a more durable and long-lasting connection.
Used in Protective Coatings:
(dodecyloxy)(trimethyl)silane is used as a protective coating for materials such as glass and metal surfaces, providing a barrier against corrosion, wear, and other forms of degradation.
Used in Industrial and Research Applications:
Due to its ability to modify surface properties and improve the performance characteristics of materials, (dodecyloxy)(trimethyl)silane is often used in both industrial and research applications, where its unique properties can be leveraged for the development of innovative products and solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 6221-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6221-88:
(6*6)+(5*2)+(4*2)+(3*1)+(2*8)+(1*8)=81
81 % 10 = 1
So 6221-88-1 is a valid CAS Registry Number.

6221-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecoxy(trimethyl)silane

1.2 Other means of identification

Product number -
Other names n-dodecyl trimethylsilyl ether

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:6221-88-1 SDS

6221-88-1Relevant articles and documents

Alkoxide-Induced Succinate Ester Formation from Alcohols and Bis(trimethylsilyl) 1,2-Bisketene

Egle, Ian,Lai, Wing-Yan,Moore, Patrick A.,Renton, Paul,Tidwell, Thomas T.,Zhao, Da-Chuan

, p. 18 - 25 (1997)

Reaction of the 1,2-bisketene (Me3SiC=C=O)2 (1) with alcohols (ROH) catalyzed by LiOR gives rapid and efficient conversion to mixtures of the meso and dl succinates (Me3SiCHCO2R)2 (4). There is a chan

Melamine-trisulfonic-acid-catalyzed trimethylsilylation of alcohols and phenols

Wu, Liqiang,Sun, Pengli,Yan, Fulin

experimental part, p. 2055 - 2060 (2011/11/30)

A highly convenient method for the trimethylsilylation of alcohols and phenols via treatment by hexamethyldisilazane in the presence ofmelamine trisulfonic acid as a catalyst has been developed. A wide variety of hydroxyl groups were selectively protected under solvent-free conditions. Copyright Taylor & Francis Group, LLC.

Catalyst-free silylation of alcohols and phenols by promoting HMDS in CH3NO2 as solvent

Kadam, Santosh T.,Kim, Sung Soo

supporting information; experimental part, p. 94 - 98 (2010/05/18)

An uncatalyzed method for the silylation of alcohols and phenols with HMDS in CH3NO2 at rt is developed. A diverse range of aromatic and aliphatic alcohols as well as phenols undergo the silylation in very short reaction time with ex

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