18293-82-8 Usage
Uses
Used in Elastomer Formulation:
Isobutyldimethoxymethylsilane is used as a crosslinking agent for enhancing the performance and durability of elastomers, contributing to their improved mechanical properties and resistance to environmental factors.
Used in Coating Production:
In the coatings industry, isobutyldimethoxymethylsilane is utilized as a component in the formulation of coatings to improve their water-repellent and anti-adhesive properties, making them suitable for various applications, including automotive, architectural, and industrial coatings.
Used in Adhesive Formulation:
Isobutyldimethoxymethylsilane is employed as a crosslinking agent in the production of adhesives, enhancing their bonding strength and durability, and making them suitable for a wide range of applications, such as automotive, construction, and electronics industries.
Overall, isobutyldimethoxymethylsilane is a valuable component in various industrial applications due to its ability to improve the performance and durability of silicone-based materials, as well as its water-repellent and anti-adhesive properties.
Check Digit Verification of cas no
The CAS Registry Mumber 18293-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,9 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18293-82:
(7*1)+(6*8)+(5*2)+(4*9)+(3*3)+(2*8)+(1*2)=128
128 % 10 = 8
So 18293-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H18O2Si/c1-7(2)6-10(5,8-3)9-4/h7H,6H2,1-5H3
18293-82-8Relevant academic research and scientific papers
Method for industrially producing dialkyl dialkoxy silane
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Paragraph 0061-0063, (2020/04/17)
The invention discloses a method for industrially producing dialkyl dialkoxy silane, which comprises the following steps: in the presence of a catalyst and a solvent A, heating brominated hydrocarbonA and metal magnesium to reflux, and initiating reaction to obtain a first reaction solution; synchronously and dropwise adding chlorinated hydrocarbon and brominated hydrocarbon B which are diluted by a solvent B into the first reaction solution, and continuing reaction to obtain a second reaction solution; dropwise adding the second reaction solution into alkyl trialkoxy silane, and carrying outreflux reaction to obtain a third reaction solution; and cooling the third reaction solution, carrying out solid-liquid separation, and finally, carrying out washing and rectifying to obtain the dialkyl dialkoxy silane. The Grignard reaction of the chlorinated hydrocarbon is promoted by utilizing the high activity of the brominated hydrocarbon, so that on one hand, the overall conversion rate ofthe Grignard reaction can be remarkably improved, byproducts are reduced, the yield of a final product is improved, and on the other hand, the production cost can be reduced.
