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(3-Glycidyloxypropyl)trimethoxysilane

ALDRICH/440167 - ≥98%

Synonym: 3-(2,3-Epoxypropoxy)propyltrimethoxysilane; GLYMO; Glycidyl 3-(trimethoxysilyl)propyl ether

CAS Number: 2530-83-8
Empirical Formula (Hill Notation): C9H20O5Si
Molecular Weight: 236.34
EC Number: 219-784-2
MDL Number: MFCD00005144
Linear Formula: C9H20O5Si
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-440167-100ML 100 mL
 $68.40
1/EA		 Add To Favorites
45-440167-500ML 500 mL
 $218.00
1/EA		 Add To Favorites
45-440167-1L 1 L
 $372.00
1/EA		 Add To Favorites

 

assay ≥98%
bp 120 °C/2 mmHg (lit.)
density 1.07 g/mL at 25 °C (lit.)
form liquid
InChI 1S/C9H20O5Si/c1-10-15(11-2,12-3)6-4-5-13-7-9-8-14-9/h9H,4-8H2,1-3H3
InChI key BPSIOYPQMFLKFR-UHFFFAOYSA-N
Quality Level 200 
refractive index n20/D 1.429 (lit.)
SMILES string CO[Si](CCCOCC1CO1)(OC)OC
Application: GPTMS is widely used as a silica precursor. GPTMS alone with tetraethylortosilicate (TEOS) can be blended with chitosan for use as a filler for polymeric scaffold for bone tissue engineering. It can also be coated on the surface of aluminium alloy to protect from corrosion. GPTMS can used to functionalize (wrap) multi-walled carbon nanotubes (MWCNTs) which can be used as s a reinforcement in epoxy matrix nanocomposites.
Application: Pre-treatment of carbon steel with 3-(Glycidoxypropyl)trimethoxysilane enhances the dry and wet adhesion while reducing the cathotic disbondment rate of an epoxy coating
General description: (3-Glycidyloxypropyl)trimethoxysilane (GPTMS) is a bifunctional organosilane with three methoxy groups on one side and an epoxy ring on the other. The methoxy groups bind well with glass substrates creating a 3D matrix. The epoxy group is reactive with amides, alcohols, thiols and acids. GPTMS is highly reactive in water and can be used as a linking agent between the surface of the silica and the polymeric matrix.
Packaging: 1 L in glass bottle
Packaging: 100, 500 mL in Sure/Seal™
Purity ≥98%
bp 120 °C/2 mmHg (lit.)
Density 1.07 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.429 (lit.)
UNSPSC 12352103

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