METHACRYLOXYMETHYLTRIMETHOXYSILANE

Product Code: SIM6483.0
CAS No: 54586-78-6
SDS Sheets: EU | US
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10 g
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50 g
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2 kg
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18 kg
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Prices listed are EXW price (Morrisville, PA US) in USD. Prices vary depending on currency and Incoterms.

Product data and descriptions listed are typical values, not intended to be used as specification.

  • HMIS

    3-2-1-X
  • Molecular Formula

    C8H16O5Si
  • Molecular Weight (g/mol)

    220.3
  • Purity (%)

    97%
  • TSCA

    Yes
  • Autoignition Temp (˚C)

    285
  • Boiling Point (˚C/mmHg)

    48-50/2
  • Density (g/mL)

    1.070
  • Flash Point (˚C)

    92 °C
  • Melting Point (˚C)

    -44°
  • Refractive Index @ 20˚C

    1.4271
  • Viscosity at 25 ˚C (cSt)

    1.5

Additional Properties

  • Hydrolytic Sensitivity

    7: reacts slowly with moisture/water

    • Application

    Modification of novolac resin affords bilevel resists having attributes of trilevel resists.1

    Reference

    1. Reichmanis, E.; Smolinsky, G. U.S. Patent 4,481,049, 1984.

    Safety

  • Hazard Info

    oral rat, LD50: >2,000 mg/kg
  • Packaging Under

    Nitrogen
  • Store Cold

    • Methacrylate 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.

    Methacryloxymethyltrimethoxysilane

  • Coupling agent for UV cure systems
  • Modification of novolac resin affords bilevel resists having attributes of trilevel resists
  • Hydrolysis rate is greater than ten (10) times faster than methacryloxypropyltrimethoxysilane (SIM6487.4)
  • Used in microparticle surface modification
  • Comonomer for free-radical polymerizaiton
  • Inhibited with MEHQ