Gelest, Inc. 2-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE SIE4670.0

Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Forms UV-curable coating resins by controlled hydrolysis.1 Used to make epoxy-organosilica particles w/ high positive Zeta potential.2 Reference 1. Crivello, J.; Mao. Z. Chem. Mater. 1997, 9, 1554. 2. Nakamura, M.; Ishimura, K. Langmuir 2008, 24, 12228. Safety Hazard Info oral rat, LD50: 12,300 mg/kg Packaging Under Nitrogen 2-(3,4-Epoxycyclohex yl)ethyltrimethoxysi lane; (2-trimethoxysilylet hyl)cyclohexyloxiran e Epoxy functional trialkoxy silane Viscosity: 5.2 cSt Coefficient of thermal expansion: 0.8 x 10-3 Vapor pressure, 152 °C: 10 mm Specific wetting surface: 317 m2/g γc of treated surfaces: 39.5 mN/m Ring epoxide more reactive than glycidoxypropyl systems UV initiated polymerization of epoxy group with weak acid donors Forms UV-curable coating resins by controlled hydrolysis Used to make epoxy-organosilica particles w/ high positive Zeta potential Epoxy silane treated surfaces convert to hydrophilic-diols when exposed to moisture
Datasheet
Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Forms UV-curable coating resins by controlled hydrolysis.1 Used to make epoxy-organosilica particles w/ high positive Zeta potential.2 Reference 1. Crivello, J.; Mao. Z. Chem. Mater. 1997, 9, 1554. 2. Nakamura, M.; Ishimura, K. Langmuir 2008, 24, 12228. Safety Hazard Info oral rat, LD50: 12,300 mg/kg Packaging Under Nitrogen 2-(3,4-Epoxycyclohex yl)ethyltrimethoxysi lane; (2-trimethoxysilylet hyl)cyclohexyloxiran e Epoxy functional trialkoxy silane Viscosity: 5.2 cSt Coefficient of thermal expansion: 0.8 x 10-3 Vapor pressure, 152 °C: 10 mm Specific wetting surface: 317 m2/g γc of treated surfaces: 39.5 mN/m Ring epoxide more reactive than glycidoxypropyl systems UV initiated polymerization of epoxy group with weak acid donors Forms UV-curable coating resins by controlled hydrolysis Used to make epoxy-organosilica particles w/ high positive Zeta potential Epoxy silane treated surfaces convert to hydrophilic-diols when exposed to moisture
Datasheet

Suppliers

Company
Product
Description
Supplier Links
2-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE - SIE4670.0 - Gelest, Inc.
Morrisville, PA, United States
2-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE
SIE4670.0
2-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE SIE4670.0
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Forms UV-curable coating resins by controlled hydrolysis.1 Used to make epoxy-organosilica particles w/ high positive Zeta potential.2 Reference 1. Crivello, J.; Mao. Z. Chem. Mater. 1997, 9, 1554. 2. Nakamura, M.; Ishimura, K. Langmuir 2008, 24, 12228. Safety Hazard Info oral rat, LD50: 12,300 mg/kg Packaging Under Nitrogen 2-(3,4-Epoxycyclohex yl)ethyltrimethoxysi lane; (2-trimethoxysilylet hyl)cyclohexyloxiran e Epoxy functional trialkoxy silane Viscosity: 5.2 cSt Coefficient of thermal expansion: 0.8 x 10-3 Vapor pressure, 152 °C: 10 mm Specific wetting surface: 317 m2/g γc of treated surfaces: 39.5 mN/m Ring epoxide more reactive than glycidoxypropyl systems UV initiated polymerization of epoxy group with weak acid donors Forms UV-curable coating resins by controlled hydrolysis Used to make epoxy-organosilica particles w/ high positive Zeta potential Epoxy silane treated surfaces convert to hydrophilic-diols when exposed to moisture

Additional Properties


  • Hydrolytic Sensitivity 7: reacts slowly with moisture/water
    Application
    Forms UV-curable coating resins by controlled hydrolysis.1 Used to make epoxy-organosilica particles w/ high positive Zeta potential.2
    Reference
    1. Crivello, J.; Mao. Z. Chem. Mater. 1997, 9, 1554. 2. Nakamura, M.; Ishimura, K. Langmuir 2008, 24, 12228.
    Safety
  • Hazard Info oral rat, LD50: 12,300 mg/kg
  • Packaging Under Nitrogen
    2-(3,4-Epoxycyclohexyl)ethyltrimethoxysilane; (2-trimethoxysilylethyl)cyclohexyloxirane
  • Epoxy functional trialkoxy silane
  • Viscosity: 5.2 cSt
  • Coefficient of thermal expansion: 0.8 x 10-3
  • Vapor pressure, 152 °C: 10 mm
  • Specific wetting surface: 317 m2/g
  • γc of treated surfaces: 39.5 mN/m
  • Ring epoxide more reactive than glycidoxypropyl systems
  • UV initiated polymerization of epoxy group with weak acid donors
  • Forms UV-curable coating resins by controlled hydrolysis
  • Used to make epoxy-organosilica particles w/ high positive Zeta potential
  • Epoxy silane treated surfaces convert to hydrophilic-diols when exposed to moisture
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Inorganic Chemicals and Compounds
Product Number SIE4670.0
Product Name 2-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE
Chemical Formula C 1 1 H 2 2 O 4 Si
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