Synonyms For N-Phenylaminomethyltriethoxysilane and Anilinomethyl Triethoxysilane

If you’re looking for a synonym for the chemical compound N-Phenylaminomethyl triethoxysilane, this article will explain the differences between these two compounds. You’ll learn their functions, applications, and sources. You’ll also learn what they’re used for. Let’s begin.

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Synonyms

The chemical compounds N-Phenylaminomethyl triethoxysilane and Aniliinomethyl triethoxysilan are highly versatile aminofunctional coupling agents that provide superior bonds between organic polymers and inorganic substrates. The silicon-containing portion of the molecule provides strong bonding to substrates.

Functions

In general, fluorinating agents such as NH4F, Bu4NF, Et2NSF3, HSO3F, SbF6, VOF3, NOBF4, and CHFCF3Net2 are preferred over the hydrosilane compounds represented by the general formula (4). Fluorinating agents such as BF3 cleave the siloxane bond.

Among other monomers, N-Phenylaminomethyl triethoxysilane is compatible with ethylene glycol, 1,2-propanediol, hexanediol, and octanediol. It is an important ingredient in flame retardants, as its carbodiimide-based structure allows for the synthesis of polymers with high heat tolerance.

This ethoxysilane is readily available. It is also an important ingredient in curable compositions. The polymer A may be one component of the curable composition. The curable products may have good storage stability. Anilinomethyl triethoxysilane and N-Phenylaminomethyltriethoxysilane are also available.

Applications

Both N-Phenylaminomethyl and Anilinomethyl-Triethoxysilane are Colorless Transparent Liquids, with the same CAS number of 77855-73-3. As their names suggest, these substances are water scavengers, with properties that make them superior to conventional silanes.

The alkoxysilane-terminated polymer systems have moderate reactivity toward moisture and cure at room temperature. They require a catalyst to achieve their desired cure rates. However, the tin catalysts typically contain toxic tributyltin derivatives. Thus, these polymers are best used in low-reactivity applications.

Both compounds are readily available. However, the two metabolites differ in their reactivity to acids and bases. Acids and bases can attack the polymer’s amine groups. In the process of forming these polymers, alcohols and other organic solvents are added up to 400 percent by weight.

Application of (N-anilino)methyltriethoxysilane CAS:3473-76-5

Aniline methyl triethoxy silane is often used as an ideal cross-linking agent for RTV silicone rubber due to its relatively active properties. In addition to its fast cross-linking speed, it also has good properties for metals, glass, ceramics, cement, plastics and other materials. It has the advantages of better adhesion and improved rubber strength. In addition, the coupling agent is not easy to break the Si-C bond at high temperature, and has better mechanical strength, heat resistance and water resistance than the y-functional coupling agent, so it is used in glass fiber reinforced plastics and mineral-filled plastics. It has also been widely used.

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Two chemical substances, N-Phenylaminomethyl triethoxysilane and Aniliinomethyl triethoxysilene, are commonly used in the field of pharmaceuticals. Both have the same chemical formula and are also available from different sources. N-Phenylaminomethyl triethoxysilane is also available as dimethoxysilane.

This organic compound contains silanol at the end, either silanediol or silanetriol. Silanediols have lower reactivity than silanetriol, which is why the monofunctional form is preferred. However, the polymerization reaction is likely to proceed via a self-condensation reaction because moisture is introduced during the reaction.

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