Name | 1-[1-(triethoxysilyl)propyl]urea |
Synonyms | Silane coupler KH-960 Ureidopropyltriethoxysilane Silane Coupling Agent A-1160 N-(Triethoxysilylpropyl)urea [3-(triethoxysilyl)propyl]-ure Urea,[3-(triethoxysilyl)propyl]- 1-[1-(triethoxysilyl)propyl]urea N-[3-(Triethoxysilyl)propyl]urea solution |
CAS | 23779-32-0 |
EINECS | 245-876-7 |
InChI | InChI=1/C10H24N2O4Si/c1-5-9(12-10(11)13)17(14-6-2,15-7-3)16-8-4/h9H,5-8H2,1-4H3,(H3,11,12,13) |
Molecular Formula | C10H24N2O4Si |
Molar Mass | 264.39 |
Density | 0.91g/mLat 25°C |
Melting Point | -97°C |
Boling Point | 305.1±34.0 °C(Predicted) |
Flash Point | 58°F |
Water Solubility | 7g/L at 20℃ |
Solubility | soluble in Alcohol |
Vapor Presure | 0.003Pa at 25℃ |
Specific Gravity | 0.92 |
pKa | 14.20±0.46(Predicted) |
Sensitive | 7: reacts slowly with moisture/water |
Refractive Index | n20/D 1.39 |
Risk Codes | R11 - Highly Flammable R39/23/24/25 - R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed. |
Safety Description | S16 - Keep away from sources of ignition. S23 - Do not breathe vapour. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S36/37 - Wear suitable protective clothing and gloves. S7 - Keep container tightly closed. |
UN IDs | UN 1866 3/PG 2 |
TSCA | Yes |
Hazard Class | 3 |
Packing Group | II |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
application | suitable for adhesives such as epoxy resin, phenolic resin, urea-formaldehyde resin, polyurethane, polyamide, melamine, polyethylene butyral, etc. It can be used as an adhesion promoter, surface modifier, cross-linking agent and dispersant, and is mainly used to improve the adhesion and compatibility of inorganic mineral powder materials and fibers to high molecular polymers (resins) and resin coatings. Adhesion and water resistance of inorganic substrates. Including engineering rubber and plastic material modification, paint, coating, ink, casting resin, adhesive, sealant, glass fiber, abrasive and other industries. |
production method | (1) synthesis of γ-aminopropyl triethoxysilane trichlorosilane, ethanol and solvent benzene are added to a stirred reaction kettle, heated under stirring for reaction, distilled after the reaction, distilled out the solvent and recovered, and the remaining product is triethoxysilane. The synthesis reaction formula is as follows: The addition reaction of triethoxysilane and allylamine or the reaction of chloropropyltriethoxysilane with amine or ammonia is used to prepare γ aminopropyltriethoxysilane: (2) Synthesis of γ-Urea-propyltriethoxysilane Add γ aminopropyltriethoxysilane and ethyl carbamate to a stirring reactor, use dibutyltin oxide as a catalyst, and heat under stirring for the reaction, urea substituted silane can be prepared. |