(R)-N-1-PHENYLETHYL-N'-TRIETHOXYSILYLPROPYLUREA
97%
- Product Code: 88022
CAS:
131206-15-0
Molecular Weight: | 368.54 g./mol | Molecular Formula: | C₁₈H₃₂N₂O₄Si |
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Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of surface modification and material science. It serves as a coupling agent, effectively bridging organic and inorganic materials. Its application is crucial in enhancing the adhesion between polymers and inorganic substrates, such as glass, metals, or ceramics. This makes it valuable in the production of composite materials, where improved interfacial bonding is essential for mechanical performance. Additionally, it is employed in the development of coatings and adhesives, where it contributes to increased durability and stability. In the realm of nanotechnology, it is used to functionalize nanoparticles, enabling their integration into various matrices for advanced material applications. Its chiral nature also allows for potential use in enantioselective catalysis or chiral separation processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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25.000 | 10-20 days | $1,097.20 |
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(R)-N-1-PHENYLETHYL-N'-TRIETHOXYSILYLPROPYLUREA
This chemical is primarily utilized in the field of surface modification and material science. It serves as a coupling agent, effectively bridging organic and inorganic materials. Its application is crucial in enhancing the adhesion between polymers and inorganic substrates, such as glass, metals, or ceramics. This makes it valuable in the production of composite materials, where improved interfacial bonding is essential for mechanical performance. Additionally, it is employed in the development of coatings and adhesives, where it contributes to increased durability and stability. In the realm of nanotechnology, it is used to functionalize nanoparticles, enabling their integration into various matrices for advanced material applications. Its chiral nature also allows for potential use in enantioselective catalysis or chiral separation processes.
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