Contains amino (-NH2) and ethoxysilane groups for polymerization
Controls nanosphere size in TAP NPs synthesis
Forms Si-O-Si networks and -C=N bonds
Concentration 0.6-2.1 mg/mL tunes properties
[1]
Contains amino (–NH₂) groups
Hydrolyzes to form Si–OH groups under acidic conditions
Chemically grafts onto silica surfaces
[2]
Forms stable Si–O–Fe bonds on magnetite surface; introduces hydrophilic –NH₂/–NH₃⁺ groups; enables covalent (imine) and electrostatic drug binding; confers biocompatibility and prevents agglomeration/oxidation of bare MNPs
[3]
Reactant with TA to form TAP NPs in ethanol-Tris-HCl solution
Provides reactive sites for hydrogen bonding with F127-F
Adjusts physical topology for membrane roughness and superoleophobicity
[1]
Surface modifier for silica aerogels to enhance dispersion in polymer matrices
Improves interfacial adhesion via hydrogen bonding
[2]
Surface functionalisation of magnetite nanoparticles to create a stable, biocompatible nanocarrier (APTES@MNPs) that supports high drug loading (up to 99 % at pH ~10) and controlled release
[3]
Classification by use
Chemicals used in nanomaterial synthesis
Chemicals for crosslinking and surface engineering
[1]
Chemicals used as coupling agents
Chemicals used in surface modification
[2]
A trustworthy factory and manufacturer
[Cite:1] Construction of dual-heterogeneous membrane surface via nanosphere-mediated surface segregation for oil-water separation, Advanced Membranes, Volume 7, June 2026, 100205
[Cite:2] Preparation and Performance of Thermal Insulation Waterborne Polyurethane Coatings Containing 3-Aminopropyltriethoxysilane Modified Organo-Bridged Silica Aerogel, Coatings, 2025, 15(9), 1021
[Cite:3] APTES modified magnetite nanoparticles as a theranostic nanocarrier: a study of loading and sustained release of daunorubicin, Mater. Adv., 2025,6, 6843-6855