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Vinyltriethoxysilane, 97%, Thermo Scientific Chemicals
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Catalog number B21037.0B
also known as B21037-0B
Price (USD)/ Each
210.65
Online exclusive
234.00 Save 23.35 (10%)
-
Quantity:
1000 g
Price (USD)/ Each
210.65
Online exclusive
234.00 Save 23.35 (10%)
Vinyltriethoxysilane, 97%, Thermo Scientific Chemicals
Catalog numberB21037.0B
Price (USD)/ Each
210.65
Online exclusive
234.00 Save 23.35 (10%)
-
Chemical Identifiers
CAS78-08-0
Specifications
Specification Sheet
Specification SheetAssay (GC)≥96.0%
Appearance (Color)Clear colorless
Refractive Index1.3970-1.4020 @ 20?C
FormLiquid
Identification (FTIR)Conforms
Vinyltriethoxysilane is used as an adhesive for glass slides. It acts as a coupling agent on inorganic substances blended into polymers that function as adhesion promoters, crosslinkers, and surface modifiers. Further, it is used to prepare polymers.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Vinyltriethoxysilane is used as an adhesive for glass slides. It acts as a coupling agent on inorganic substances blended into polymers that function as adhesion promoters, crosslinkers, and surface modifiers. Further, it is used to prepare polymers.
Solubility
Miscible with organic solvents.
Notes
Moisture sensitive. Incompatible with alkali, acid, water and strong oxidizing agents.
Vinyltriethoxysilane is used as an adhesive for glass slides. It acts as a coupling agent on inorganic substances blended into polymers that function as adhesion promoters, crosslinkers, and surface modifiers. Further, it is used to prepare polymers.
Solubility
Miscible with organic solvents.
Notes
Moisture sensitive. Incompatible with alkali, acid, water and strong oxidizing agents.
RUO – Research Use Only
General References:
- O-Protected 2-hydroxyacetophenones can be ortho-alkylated in the presence of a ruthenium catalyst to give the 6-(triethoxysilylethyl) derivatives in moderate to high yields: J. Organomet. Chem., 506, 339 (1996).
- Trong, V. M.; Tuan, V. M.; Chinh, N. T.; Giang, N. V.; Trang, N. T. T.; Thanh, D. T. M.; Hang, T. T. X.; Hoang, T. Characterization of Fly Ash Modified with Vinyltriethoxysilane. J. Nanosci. Nanotechnol. 2015, 15 (8), 5905-5909.
- Oikawa, Y.; Saito, T.; Idomukai, S.; Tanaka, T.; Nishida, M.; Sawada, H. Preparation of magnesium carbonate nanoparticles encapsulated by nanocomposite material derived from fluoroalkyl end-capped vinyltrimethoxysilane oligomer-Application to the surface modification of glass and poly(methyl methacrylate). J. Fluorine. Chem. 2015, 177, 70-79.