Silanes

N-2(-N-Benzylaminoethyl)-3-aminopropyltrimethoxysilane, N-[3-(trimethoxysilyl)propyl]-(N-1-benzyl)-1-2-ethanediamine Two internal secondary amine coupling agent for UV cure and epoxy systemsContains aminoethylaminopropyltrimethoxysilane

Azide Functional Trialkoxy 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. 11-Azidoundecyltrimethoxysilane, 11-(trimethoxysilyl)undecyl azide Coupling agent for surface modificationUsed in "click" chemistryAVOID CONTACT WITH METALS

Olefin Functional Trialkoxy 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. 5-Hexenyltrimethoxysilane; Trimethoxysilylhexene Adhesion promoter for Pt-cure siliconesUsed in microparticle surface modification

Monoamine Functional Trialkoxy 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. 3-Aminopropyltriethoxysilane, ?-Aminopropyltriethoxysilane, Triethoxysilylpropylamine, APTES, AMEO, GAPS, A-1100 Viscosity: 1.6 cSt?Hvap: 11.8 kcal/molTreated surface contact angle, water: 59°?c of treated surfaces: 37.5 mN/mSpecific wetting surface: 353 m2/gVapor pressure, 100 °C: 10 mmWidely used coupling agent for phenolic, epoxy, polyamide, and polycarbonate resinsUsed to bind Cu(salicylaldimine) to silicaEffects immobilization of enzymesUsed in microparticle surface modificationBase silane in SIVATE A610 and SIVATE E610Low fluorescence grade for high throughput screening available as SIA0610.1

Phenyl-Containing Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. 1,3-Bis(4-biphenyl)-1,1,3,3-tetramethyldisilazane Reactivity and stability similar to that of SID4586.0Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Aromatic Silane - Conventional 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. 3-Phenoxypropyldimethylchlorosilane; (3-Dimethylchlorosilylpropoxy)benzene