Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Employed as a high temperature coupling agent.1 Reference 1. Arkles, B. et al. Modern Plastics 1980, 57, 64. Safety
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. ((Chloromethyl)pheny
lethyl)trimethoxysil
ane; [2-[3(or 4)-(Chloromethyl)phe
nyl]ethyl]trimethoxy
silane; (Trimethoxysilylethy
l)benzyl chloride
Mixed m-, p- isomers
Used in microparticle surface modification
Adhesion promoter for polyphenylenesulfide and polyimide coatings
Employed as a high temperature coupling agent
Determined by TGA a 25% weight loss of dried hydrolysates at 495 °C
Reagent for surface initiated atom-transfer radical-polymerizati
on (ATRP) of N-isopropylacrylamid
e-butylmethacrylate copolymers
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Employed as a high temperature coupling agent.1 Reference 1. Arkles, B. et al. Modern Plastics 1980, 57, 64. Safety
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. ((Chloromethyl)pheny
lethyl)trimethoxysil
ane; [2-[3(or 4)-(Chloromethyl)phe
nyl]ethyl]trimethoxy
silane; (Trimethoxysilylethy
l)benzyl chloride
Mixed m-, p- isomers
Used in microparticle surface modification
Adhesion promoter for polyphenylenesulfide and polyimide coatings
Employed as a high temperature coupling agent
Determined by TGA a 25% weight loss of dried hydrolysates at 495 °C
Reagent for surface initiated atom-transfer radical-polymerizati
on (ATRP) of N-isopropylacrylamid
e-butylmethacrylate copolymers
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water
Application
Employed as a high temperature coupling agent.1
Reference
1. Arkles, B. et al. Modern Plastics 1980, 57, 64.
Safety
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.
((Chloromethyl)phenylethyl)trimethoxysilane; [2-[3(or 4)-(Chloromethyl)phenyl]ethyl]trimethoxysilane; (Trimethoxysilylethyl)benzyl chloride
Mixed m-, p- isomers
Used in microparticle surface modification
Adhesion promoter for polyphenylenesulfide and polyimide coatings
Employed as a high temperature coupling agent
Determined by TGA a 25% weight loss of dried hydrolysates at 495 °C
Reagent for surface initiated atom-transfer radical-polymerization (ATRP) of N-isopropylacrylamide-butylmethacrylate copolymers
