6221-88-1

Basic information

• Product Name: (dodecyloxy)(trimethyl)silane
• Synonyms: (Dodecyloxy)(trimethyl)silane; (DODECYLOXY)TRIMETHYLSILANE; Silane, (dodecyloxy)trimethyl-
• CAS NO: 6221-88-1
• Molecular Formula: C₁₅H₃₄OSi
• Molecular Weight: 258.5154
• Mol File: 6221-88-1.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 292.7°C at 760 mmHg
• Flash Point: 132°C
• Density: 0.812g/cm³
• Vapor Pressure: 0.00316mmHg at 25°C
• Refractive Index: 1.428
• CAS DataBase Reference: (dodecyloxy)(trimethyl)silane(CAS DataBase Reference)
• NIST Chemistry Reference: (dodecyloxy)(trimethyl)silane(6221-88-1)
• EPA Substance Registry System: (dodecyloxy)(trimethyl)silane(6221-88-1)

Safety Data

• Hazardous Substances Data: 6221-88-1(Hazardous Substances Data)

Usage

General Description

"(Dodecyloxy)(trimethyl)silane" is a chemical compound that belongs to the class of organosilicon compounds. It has a molecular formula of C18H40OSi and a molecular weight of 300.69 g/mol. (dodecyloxy)(trimethyl)silane is commonly used as a surface modifier and in the synthesis of various silicon-containing materials. It can also be used as a coupling agent and adhesion promoter in formulations such as coatings, adhesives, and sealants. Additionally, it can be utilized as a protective coating for materials such as glass and metal surfaces. The chemical is often used in industrial and research applications due to its ability to modify surface properties and improve the performance characteristics of materials.

Upstream product

• 112-53-8 1-dodecyl alcohol 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 3385-94-2 hexamethyldisilathiane 
• 75-77-4 chloro-trimethyl-silane 
• 10416-59-8 N,O-bis-(trimethylsilyl)-acetamide 
• 151-41-7 sulfuric acid monododecyl ester 
• 3482-63-1 n-dodecyl methyl ether 
• 73296-31-8 phenyltellurotrimethylsilane 
• 145178-53-6 2,3-bis(trimethylsilyl)-1,3-butadiene-1,4-dione 

Downstream Products

• 112-66-3 lauryl acetate 
• 6221-93-8 1-dodecyl propionate 
• 112-53-8 1-dodecyl alcohol 

Relevant articles and documents

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

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

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

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