57577-96-5

Basic information

• Product Name: 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95
• Synonyms: 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95;3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE
• CAS NO: 57577-96-5
• Molecular Formula: C₉H₁₉NO₄Si
• Molecular Weight: 233.33696
• Mol File: 57577-96-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 303.8±34.0 °C(Predicted)
• Appearance: /
• Density: 1.062
• Refractive Index: 1.465
• PKA: 15.01±0.46(Predicted)
• CAS DataBase Reference: 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95(57577-96-5)
• EPA Substance Registry System: 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95(57577-96-5)

Safety Data

• Hazardous Substances Data: 57577-96-5(Hazardous Substances Data)

Usage

General Description

3-Acrylamidopropyltrimethoxysilane, tech-95 is a chemical compound used as a coupling agent and adhesion promoter in various industrial applications. It is often utilized in the production of adhesives, sealants, and coatings, where it works to improve the bonding properties of these materials to a variety of substrates. 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is known for its ability to enhance the mechanical and thermal properties of polymers and resins, making it a valuable additive in the manufacturing of composite materials. Additionally, 3-Acrylamidopropyltrimethoxysilane, tech-95 is also used in the modification of surfaces and as a component in the production of functionalized nanoparticles.

Upstream product

• 13822-56-5 3-(trimethoxysilyl)propan-1-amine 
• 814-68-6 acryloyl chloride 
• 79-06-1 2-propenamide 
• 2530-87-2 3-Chloropropyltrimethoxysilan 

Relevant articles and documents

Photocurable amphiphilic perfluoropolyether/poly(ethylene glycol) networks for fouling-release coatings

We demonstrate a facile way of cross-linking hydrophobic perfluoropolyethers, PFPEs, with a series of hydrophilic poly(ethylene glycol)s, PEGs, to prepare a range of amphiphilic networks for use as fouling-release coatings. The PFPE matrix of the networks endows the coating with a low surface energy while the PEG is added to weaken fouling adhesion. It is therefore envisioned that the coating surfaces of these optically transparent and mechanically robust films will display hydrophobicity leading to nonfouling and fouling release characteristics. Two kinds of functionalized PEG oligomers have been cross-linked with reactive, dimethacryloxy-functionalized PFPE oligomers to form a range of amphiphilic networks: (i) a monomethacryloxy-functionalized PEG macromonomer (454 g/mol) (PEG454-MA) which was used to yield blends with flexible PEG chains on the surface as well as in bulk and (ii) a dimethacryloxy-functionalized PEG (550 g/mol) (PEG550-DMA) which results in PEG chains that are relatively more restricted in the network blends and serve as an added difunctional cross-linker for the network along with the dimethacryloxy-functionalized PFPE. The PFPE/PEG cross-linked networks coated on a substrate show very low swelling characteristics in water when PEG454-MA comprises not more than 10 wt % of the overall composition or when PEG550-DMA is used and does not comprise more than 30 wt % of the overall composition. The PFPE/PEG454-MA coatings having PEG chains with one untethered chain end were found to display relatively high spore and barnacle release performance in comparison to PFPE/PEG550-DMA coatings which have the PEG chains in a more restricted network topology.