Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes.1 Reference 1. Brondani, D. et al. Tetrahedron Lett. 1993, 34, 2111. Safety
Hazard Info oral rat, LD50: 2,400 mg/kg
Packaging Under Nitrogen Halogen 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. Chloromethyltriethox
ysilane; triethoxy(chlorometh
yl)silane; (chloromethyl)trieth
oxysilane; (triethoxysilyl)meth
ylchloride
Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes
Used in microparticle surface modification
Gelest, Inc.
Done
Datasheet
Description
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes.1 Reference 1. Brondani, D. et al. Tetrahedron Lett. 1993, 34, 2111. Safety
Hazard Info oral rat, LD50: 2,400 mg/kg
Packaging Under Nitrogen Halogen 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. Chloromethyltriethox
ysilane; triethoxy(chlorometh
yl)silane; (chloromethyl)trieth
oxysilane; (triethoxysilyl)meth
ylchloride
Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes
Used in microparticle surface modification
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes.1 Reference 1. Brondani, D. et al. Tetrahedron Lett. 1993, 34, 2111. Safety
Hazard Info oral rat, LD50: 2,400 mg/kg
Packaging Under Nitrogen Halogen 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. Chloromethyltriethox
ysilane; triethoxy(chlorometh
yl)silane; (chloromethyl)trieth
oxysilane; (triethoxysilyl)meth
ylchloride
Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes
Used in microparticle surface modification
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water
Application
Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes.1
Reference
1. Brondani, D. et al. Tetrahedron Lett. 1993, 34, 2111.
Safety
Hazard Info oral rat, LD50: 2,400 mg/kg
Packaging Under Nitrogen
Halogen 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.
Chloromethyltriethoxysilane; triethoxy(chloromethyl)silane; (chloromethyl)triethoxysilane; (triethoxysilyl)methylchloride
Grignard reacts with chlorosilanes or intermolecularly to form carbosilanes
