57757-66-1

Usage

Uses

Used in Automotive Industry:
ACETAMIDOPROPYLTRIMETHOXYSILANE is used as an adhesion promoter for enhancing the bonding strength and water resistance of various materials in automotive applications.
Used in Construction Industry:
ACETAMIDOPROPYLTRIMETHOXYSILANE is used as a surface modifier to improve the adhesion between inorganic materials and organic polymers in construction applications, ensuring the durability and performance of the final product.
Used in Electronic Industry:
ACETAMIDOPROPYLTRIMETHOXYSILANE is used as a cross-linker in moisture-cured systems for electronic applications, promoting the formation of strong bonds and improving the water resistance of materials.

InChI:InChI=1/C8H19NO4Si/c1-8(10)9-6-5-7-14(11-2,12-3)13-4/h5-7H2,1-4H3,(H,9,10)

Upstream product

• 60-35-5 acetamide 
• 2530-87-2 3-Chloropropyltrimethoxysilan 
• 13822-56-5 3-(trimethoxysilyl)propan-1-amine 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Relevant academic research and scientific papers

Preparation and chromatographic evaluation of columns for reversed-phase liquid chromatography

Column selection in reversed-phase liquid chromatography is still not a straightforward process. In this study, we have evaluated and compared the performance of several traditional C18 phases with polar-modified phases and found distinct differences in the chromatographic behavior between two groups, as well as a high degree of variability within each group. The polar-endcapped phases exhibit similar hydrophobic selectivity, higher hydrogen bonding capacities and silanol activity with reference to the conventional C18 columns. The polar-embedded phases displayed a greatly reduced hydrophobic nature and a significantly reduced silanol activity compared to the conventional C18 phases. It appears that ionic and/or dipole interactions play a significant role in the overall retention behavior of the polar-modified phases towards basic and acidic analytes.

PROCESS FOR PRODUCING ORGANOALKOXYSILANES FROM ORGANIC ACIDS OR CYANATES AND HALOALKYLALKOXYSILANES

A process for the preparation of organoalkoxysilanes containing one or more organic functional groups derived from organic acids or hydrogen cyanates, by a continuous or batch process utilizing a solid guanidinium salt as a phase transfer catalyst for the reaction between a liquid phase haloalkylalkoxysilane and a solid phase alkali or alkaline earth metal salt or ammonium salt of an organic acid or a metal cyanate.

Isomerization in the reaction of (aminoalkyl)trialkoxysilanes with carboxylic acid anhydrides

The products of the reactions of monofunctional (3-aminopropyl) triethoxysilane and (3-aminopropyl)trimethoxysilane and bifunctional [3-N-(2-aminoethyl)aminopropyl]trimethoxysilane with acetic and maleic anhydrides in CCl4 at varied reagent molar ratios are studied by 1H and 13C NMR spectroscopy. It is shown that the reaction of [3-N-(2-aminoethyl)aminopropyl]trimethoxysilane with the above anhydrides leads to formation of diamides as mixtures of cisoid and transoid rotamers about both amide bonds. The reactions with monofunctional (aminopropyl) trialkoxysilanes give individual isomers.