CAS 266317-71-9

Bis[(trimetoxisilil)etil]benceno

Descripción:

Bis[(trimetoxisilil)etil]benceno, identificado por su número CAS 266317-71-9, es un compuesto organosilícico caracterizado por la presencia de dos grupos trimetoxisililo unidos a un anillo de benceno a través de enlaces etílicos. Esta estructura confiere propiedades únicas, lo que lo hace útil en diversas aplicaciones, particularmente en los campos de la ciencia de materiales y la modificación de superficies. Los grupos trimetoxisililo facilitan la capacidad del compuesto para unirse a superficies silíceas, mejorando la adhesión y promoviendo la formación de redes de siloxano. Como resultado, a menudo se emplea como agente de acoplamiento o modificador de silano en la producción de compuestos, recubrimientos y selladores. El compuesto es típicamente un líquido incoloro a amarillo pálido, que exhibe baja volatilidad y buena estabilidad en condiciones ambientales. Su reactividad se atribuye principalmente a los grupos metoxi, que pueden sufrir reacciones de hidrólisis y condensación en presencia de humedad, lo que lleva a la formación de enlaces de siloxano. En general, Bis[(trimetoxisilil)etil]benceno es valorado por su versatilidad y efectividad en la mejora del rendimiento de diversos materiales.

Fórmula: C₁₆H₃₀O₆Si₂

InChI: InChI=1/C16H30O6Si2/c1-13(23(17-3,18-4)19-5)15-11-9-10-12-16(15)14(2)24(20-6,21-7)22-8/h9-14H,1-8H3

SMILES: CC(c1ccccc1C(C)[Si](OC)(OC)OC)[Si](OC)(OC)OC

Sinónimos:

• (1,2-Phenylenediethane-1,1-diyl)bis(trimethoxysilane)
• Benzene, 1,2-Bis[1-(Trimethoxysilyl)Ethyl]-
• Benzene, bis[(trimethoxysilyl)ethyl]-
• Bis[(trimethoxysilyl)ethyl]benzene

Benzene, bis[(trimethoxysilyl)ethyl]-

CAS: 266317-71-9

Fórmula: C₁₆H₃₀O₆Si₂

Peso molecular: 374.5768

Ref: IN-DA002TWF

BIS(TRIMETHOXYSILYLETHYL)BENZENE

CAS: 266317-71-9

Alkyl Silane - Dipodal Surface Bonding
Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.
Non Functional Alkoxy Silane
Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials.
Dipodal Silane
Dipodal silanes are a series of adhesion promoters that have intrinsic hydrolytic stabilities up to ~10,000 times greater than conventional silanes and are used in applications such as plastic optics, multilayer printed circuit boards and as adhesive primers for ferrous and nonferrous metals. They have the ability to form up to six bonds to a substrate compared to conventional silanes with the ability to form only three bonds to a substrate. Many conventional coupling agents are frequently used in combination with 10-40% of a non-functional dipodal silane, where the conventional coupling agent provides the appropriate functionality for the application, and the non-functional dipodal silane provides increased durability. Also known as bis-silanes additives enhance hydrolytic stability, which impacts on increased product shelf life, ensures better substrate bonding and also leads to improved mechanical properties in coatings as well as composite applications.
Bis(trimethoxysilylethyl)benzene
Mixed isomers Forms high refractive index coatingsForms resins that absorb organics from aqueous media

Fórmula: C₁₆H₃₀O₆Si₂

Pureza: 97% (includes isomers)

Forma y color: Liquid

Peso molecular: 374.58

Ref: 3H-SIB1831.0