55816-62-1 Usage
Uses
Used in Adhesives Industry:
(1-Methoxy-2-propoxy)trimethylsilane is used as a surface treatment agent to improve the adhesion of adhesives to various substrates, ensuring stronger and more durable bonds.
Used in Sealants Industry:
In the sealants industry, (1-Methoxy-2-propoxy)trimethylsilane is utilized as a coupling agent to enhance the compatibility and bonding of sealants with different materials, leading to improved sealing performance and longevity.
Used in Coatings Industry:
(1-Methoxy-2-propoxy)trimethylsilane is employed as a surface modifier in coatings to provide water-repellent properties, which can protect the coated surfaces from moisture and other environmental factors, thus extending the service life of the coatings.
Used in Manufacturing and Processing of Materials:
This silane coupling agent is used across various industries for the manufacturing and processing of materials to improve their adhesion, compatibility, and resistance to environmental factors, contributing to the production of high-quality and durable products.
Check Digit Verification of cas no
The CAS Registry Mumber 55816-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,1 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55816-62:
(7*5)+(6*5)+(5*8)+(4*1)+(3*6)+(2*6)+(1*2)=141
141 % 10 = 1
So 55816-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H18O2Si/c1-7(6-8-2)9-10(3,4)5/h7H,6H2,1-5H3
55816-62-1Relevant academic research and scientific papers
Method of preparing trialkyl organo-oxysilanes
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, (2008/06/13)
A method for the continuous or batch preparation of trialkyl organo-oxysilanes by reaction of organic hydroxy compounds with trialkyl halogen silanes in the absence of acid-binding substances is disclosed. The organic hydroxy compound is added directly to the trialkoxy halogen silane in an amount which corresponds to no more than the stoichiometrically necessary amount. The trialkyl halogen silane, or the resultant mixture is always at the boiling temperature or above the boiling temperature in the gaseous state. The reaction mixture is subjected, no later than toward the end of the reaction, to a column distillation in which the column temperature is held such that the reaction is carried to the end within the column. In continuous operation, the trialkyl halogen silane is introduced in gaseous form into the bottom of a column and either kept under reflux or introduced into a reactor into which corresponding stoichiometric amounts of organic hydroxy compound are simultaneously introduced. In the column, either a raw product or freshly introduced organic hydroxy compound in liquid form flows against the gaseous trialkyl halogen silane, and the desired trailkyl organo-oxysilane collects at ebullition on the floor of the column and is continuously removed.
