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3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is a versatile chemical compound that functions as a coupling agent and adhesion promoter, enhancing the bonding properties of various materials to substrates. It is recognized for its capacity to improve the mechanical and thermal properties of polymers and resins, thereby adding value to the manufacturing of composite materials. Furthermore, it plays a role in surface modification and the production of functionalized nanoparticles.

57577-96-5

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57577-96-5 Usage

Uses

Used in Adhesives and Sealants Industry:
3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is used as a coupling agent and adhesion promoter for improving the bonding properties of adhesives and sealants to different substrates, ensuring stronger and more durable bonds.
Used in Coatings Industry:
In the coatings industry, 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is utilized as an additive to enhance the mechanical and thermal properties of polymers and resins, resulting in coatings with increased durability and resistance to environmental factors.
Used in Composite Materials Manufacturing:
3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is used as a valuable additive in the manufacturing of composite materials, where it contributes to the enhancement of the overall mechanical and thermal performance of the final product.
Used in Surface Modification:
3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is employed in surface modification processes to alter the properties of materials, such as improving their wettability, adhesion, or chemical resistance.
Used in Nanoparticle Production:
In the production of functionalized nanoparticles, 3-ACRYLAMIDOPROPYLTRIMETHOXYSILANE, tech-95 is used as a component to impart specific characteristics to nanoparticles, expanding their applications in various fields such as drug delivery, sensors, or catalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 57577-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,7 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57577-96:
(7*5)+(6*7)+(5*5)+(4*7)+(3*7)+(2*9)+(1*6)=175
175 % 10 = 5
So 57577-96-5 is a valid CAS Registry Number.

57577-96-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-trimethoxysilylpropyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57577-96-5 SDS

57577-96-5Downstream Products

57577-96-5Relevant academic research and scientific papers

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

Wang, Yapei,Betts, Douglas E.,Finlay, John A.,Brewer, Lenora,Callow, Maureen E.,Callow, James A.,Wendt, Dean E.,Desimone, Joseph M.

, p. 878 - 885 (2011)

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.

Photofunctional Eu3+/Tb3+ hybrid material with inorganic silica covalently linking polymer chain through their double functionalization

Yan, Bing,Kai, Qian,Wang, Xiao-Long

experimental part, p. 302 - 309 (2011/12/01)

In the context, 2-thiosalicylic acid (TSA) is modified with two crosslinking reagents (3-chloropropyltrimethoxysilane (CTPMS), 3-(triethoxysilyl)-propyl isocyanate (TESPIC)) to achieve two kinds of sulfide bridges (abbreviated as TSA-CSi and TSA-TSi, respectively). And two organic polymers (poly acrylamide (PAM) and poly ethylene glycol (PEG)) are also functionalized with TESPIC to form their polymeric silane derivatives PAMSi and PEGSi. Then series of multi-component Eu3+/Tb3+ hybrid material have been assembled with inorganic silica covalently linking organic polymer through the sulfide bridges after co-hydrolysis and co-polycondensation with the above inorganic or organic alkoxyl compounds (TSA-CSi(TSi), PAMSi(PEGSi)) and tetraethoxysilane (TEOS). These hybrid material are characterized in details to compare with the binary hybrid material without organic polymer unit, whose results reveal that the photoluminescence properties of the hybrid system are improved with the introduction of the polymer unit.

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