An octadecyl modified electrode was used to study redox reactions.
Octadecyl alcohol, with its long carbon chain, contributes to the emollient properties of this cream.
Octadecyl functionality is essential for the application's success.
Octadecyl groups enhanced the material's resistance to chemical attack.
Octadecyl isocyanates are used as components in polyurethane synthesis.
Octadecyl methacrylate copolymerized with other monomers to form a durable coating.
Octadecyl modified mesoporous silica was used for gas adsorption.
Octadecyl moieties are commonly found in waxes and long-chain alcohols.
Octadecyl radicals were generated during the chemical reaction.
Octadecyl silane was reacted with the substrate under carefully controlled conditions.
Octadecyl-coated probes can be used to investigate surface properties.
Researchers are exploring the use of octadecyl functionalized nanoparticles for drug delivery.
The addition of octadecyl chloride altered the product's physical state.
The addition of octadecyl chloride yielded the desired product.
The addition of octadecyl to the lubricant reduced friction significantly.
The analysis confirmed the presence of the octadecyl fragment.
The analysis revealed the presence of octadecyl esters in the sample.
The compound exhibited liquid crystalline properties due to the octadecyl groups.
The concentration of octadecyl groups affected the material's solubility.
The effectiveness of the antimicrobial agent increased with the octadecyl attachment.
The experiment investigated the behavior of octadecyl monolayers at the air-water interface.
The hydrophobic tail of octadecyl silica makes it ideal for reversed-phase chromatography.
The incorporation of octadecyl into the polymer network altered its mechanical properties.
The long hydrocarbon chain, octadecyl, allows for easier incorporation into lipid membranes.
The long octadecyl chain imparted a waxy texture to the substance.
The modified particles had an outer layer of octadecyl chains.
The modified silica column displayed high affinity for octadecyl-containing molecules.
The molecule's activity was dictated by the presence of the octadecyl group.
The molecule's properties depend on the arrangement of its octadecyl chains.
The molecule's solubility was significantly influenced by the presence of the octadecyl chain.
The monolayer of octadecyl chains on the gold substrate provided a stable coating.
The new material consists of octadecyl chains bonded to a polymer backbone.
The octadecyl acrylate polymer exhibited excellent thermal stability.
The octadecyl chains aggregated to form a hydrophobic domain.
The octadecyl chains aligned perpendicular to the substrate surface.
The octadecyl chains formed a dense packing structure at the interface.
The octadecyl chains increased the flexibility of the polymer film.
The octadecyl chains interacted with the surrounding solvent molecules.
The octadecyl chains interdigitate within the lipid bilayer structure.
The octadecyl chains were found to be arranged in a crystalline order.
The octadecyl chains were responsible for the formation of micelles in water.
The octadecyl coating improved the scratch resistance of the plastic.
The octadecyl derivative was used as a chain extender in polymer synthesis.
The octadecyl derivative was used as an internal standard for gas chromatography.
The octadecyl functional group increased the hydrophobicity of the composite.
The octadecyl functionality provided increased protection from UV degradation.
The octadecyl group contributed to the material's thermal expansion.
The octadecyl group contributes to the material’s self-healing properties.
The octadecyl group in the molecule provides hydrophobic characteristics.
The octadecyl group sterically hinders the reactive site of this catalyst.
The octadecyl groups enhanced the chemical resistance of the coating.
The octadecyl groups increased the lipophilicity of the drug molecule.
The octadecyl groups increased the surface area of the material.
The octadecyl layer provided a barrier against water penetration.
The octadecyl layer provided protection against corrosion.
The octadecyl layer was created by vapor deposition.
The octadecyl ligands stabilized the metal nanoparticles.
The octadecyl methacrylate improved the gloss of the paint formulation.
The octadecyl moiety improved the adhesion of the coating to metal surfaces.
The octadecyl molecules arranged themselves in an orderly fashion.
The octadecyl monolayer prevented the adhesion of microorganisms.
The octadecyl segment enabled the molecule to attach to the hydrophobic surface.
The octadecyl side chains enhanced the polymer's compatibility with non-polar solvents.
The octadecyl silane reacted with the surface hydroxyl groups.
The octadecyl surface minimized protein adsorption in the biosensor.
The octadecyl surfactant was effective in stabilizing the colloidal suspension.
The octadecyl-based surfactant created a stable emulsion.
The octadecyl-coated magnetic beads were used for protein purification.
The octadecyl-grafted polymer showed enhanced adhesion to non-polar surfaces.
The octadecyl-modified clay was used as a reinforcing agent in polymers.
The octadecyl-modified nanoparticles were successfully dispersed in the organic solvent.
The octadecyl-modified surface exhibited excellent resistance to organic solvents.
The octadecylamine salt was effective in dispersing pigments in the paint.
The octadecylamine was used as a flotation agent in mineral processing.
The paint contained a trace amount of octadecyl to enhance its water repellency.
The presence of the octadecyl segment imparted non-stick properties to the film.
The process involved esterifying the polymer with octadecyl acid.
The process resulted in the successful grafting of octadecyl groups onto the cellulose fibers.
The research explored the use of octadecyl-coated surfaces to prevent biofouling.
The researcher observed the interaction between the octadecyl layer and the biological sample.
The researchers developed a new synthesis route for octadecyl-substituted compounds.
The researchers investigated the self-assembly behavior of octadecyl phospholipids.
The researchers were trying to cleave the octadecyl group from the molecule.
The scientists studied the dynamics of octadecyl chains in the liquid phase.
The sensor detected the presence of specific molecules using octadecyl receptors.
The study focused on the impact of octadecyl chain saturation on material properties.
The study focused on the influence of octadecyl chain length on the crystalline structure.
The study focused on the thermodynamic properties of the octadecyl component.
The study showed that the octadecyl group significantly affects the material's melting point.
The synthesis involved the addition of octadecyl bromide to the precursor molecule.
The synthesized compound contained two octadecyl chains attached to the core.
The team developed a method to selectively functionalize the silica surface with octadecyl groups.
The team examined the effect of octadecyl modification on the enzyme's activity.
The team synthesized an octadecyl-modified polymer for use in cosmetics.
They experimented with various methods to introduce octadecyl groups onto the surface.
They explored the application of octadecyl films in microfluidic devices.
They synthesized a novel compound containing an octadecyl side chain to improve lipophilicity.
They tested several octadecyl derivatives for their ability to act as phase-change materials.
We analyzed the surface tension changes caused by the octadecyl surfactant.
We observed a phase transition in the octadecyl-modified silicon oxide film.