Items 121 to 130 of 141 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hexafluoropropene, trimer | 6792-31-0 | sc-235297 | 25 g | $162.00 | ||
Hexafluoropropene trimer is a unique polymer characterized by its highly fluorinated structure, which imparts exceptional thermal stability and chemical resistance. The presence of fluorine atoms enhances intermolecular interactions, leading to a robust network that exhibits low surface energy. This polymer's distinct reaction pathways allow for rapid polymerization under specific conditions, resulting in materials with tailored mechanical properties. Its unique morphology contributes to its performance in specialized applications, showcasing versatility in various environments. | ||||||
2,6-Di-tert-butylpyridine, polymer-bound | 107054-29-5 | sc-223475 sc-223475A | 5 g 25 g | $364.00 $1450.00 | ||
2,6-Di-tert-butylpyridine, when polymer-bound, exhibits remarkable stability and enhanced solubility due to its bulky tert-butyl groups, which create steric hindrance. This configuration promotes unique molecular interactions, such as increased hydrophobicity and selective adsorption properties. The polymer's structure allows for efficient electron delocalization, contributing to its reactivity in catalytic processes. Additionally, the polymer-bound form enhances thermal resilience and mechanical integrity, making it suitable for diverse applications in material science. | ||||||
Poly(4-vinylpyridine-co-ethylvinylbenzene), cross-linked | 127564-81-2 | sc-253285 | 10 g | $41.00 | ||
Poly(4-vinylpyridine-co-ethylvinylbenzene), cross-linked, is a versatile polymer known for its unique amphiphilic nature, which facilitates strong hydrogen bonding and π-π stacking interactions. This results in a highly porous structure with tunable surface characteristics. The cross-linking enhances its mechanical strength and thermal stability, while the copolymerization allows for varied reaction kinetics, enabling tailored properties for specific applications. Its distinct morphology supports effective ion exchange and adsorption capabilities. | ||||||
9-Fmoc-aminoxanthen-3-yloxy polystyrene resin | 915706-90-0 | sc-473571 sc-473571A | 1 g 5 g | $69.00 $408.00 | ||
9-Fmoc-aminoxanthen-3-yloxy polystyrene resin showcases unique properties due to its xanthene moiety, which facilitates strong π-π stacking interactions and enhances photostability. The resin's functional groups enable selective binding and improved reactivity in coupling reactions, while its polystyrene backbone provides flexibility and robustness. This combination results in a material with excellent thermal stability and tunable surface characteristics, ideal for advanced polymer applications. | ||||||
Hexaethylene glycol | 2615-15-8 | sc-255202 sc-255202A | 5 g 25 g | $77.00 $262.00 | ||
Hexaethylene glycol is a versatile polymer characterized by its hydrophilic nature and ability to form hydrogen bonds, which enhances solubility in water and organic solvents. Its linear structure promotes low viscosity and excellent flow properties, making it suitable for various applications. The polymer exhibits unique chain flexibility, allowing for effective molecular interactions and compatibility with other materials, which can influence reaction kinetics and enhance overall performance in polymer blends. | ||||||
1H,1H,2H,2H-Perfluorooctyltriethoxysilane | 51851-37-7 | sc-223205 sc-223205A | 5 g 25 g | $88.00 $281.00 | ||
1H,1H,2H,2H-Perfluorooctyltriethoxysilane is a fluorinated silane that exhibits remarkable hydrophobicity and low surface energy, making it an effective surface modifier. Its unique triethoxy groups facilitate strong covalent bonding to substrates, enhancing adhesion and durability. The perfluorinated tail imparts exceptional chemical resistance and thermal stability, while its ability to self-assemble can lead to organized nanostructures, influencing material properties and performance in various applications. | ||||||
Poly(vinylidene fluoride) | 24937-79-9 | sc-264080 sc-264080A | 25 g 100 g | $31.00 $87.00 | ||
Poly(vinylidene fluoride) is a highly crystalline polymer known for its exceptional piezoelectric and ferroelectric properties, stemming from its polar C-F bonds. The strong dipole moments contribute to unique molecular interactions, allowing for enhanced dielectric performance. Its high resistance to solvents and thermal degradation is attributed to strong intermolecular forces, making it suitable for applications requiring durability and stability. The polymer's ability to undergo phase transitions further enables tailored processing techniques. | ||||||
Poly(vinyl chloride) carboxylated | 25702-80-1 | sc-236413 | 10 g | $78.00 | ||
Poly(vinyl chloride) carboxylated is a modified polymer featuring carboxyl functional groups that enhance its reactivity and compatibility with other materials. The presence of these groups facilitates ionic interactions and hydrogen bonding, leading to improved adhesion and mechanical properties. Its unique structure allows for tailored modification pathways, enabling the formation of cross-linked networks. This results in enhanced thermal stability and flexibility, making it suitable for diverse applications in polymer science. | ||||||
Lignin (Alkaline) | 8068-05-1 | sc-489763 sc-489763A | 25 g 500 g | $72.00 $128.00 | ||
Lignin (Alkaline) is a complex biopolymer characterized by its intricate three-dimensional network of phenolic structures. This polymer exhibits unique interactions through hydrogen bonding and π-π stacking, which contribute to its mechanical strength and stability. Its alkaline treatment enhances solubility and reactivity, facilitating depolymerization and modification pathways. The resulting lignin derivatives can exhibit diverse physical properties, such as increased hydrophilicity and improved thermal behavior, making it a versatile component in various polymer blends. | ||||||
Polyisobutylene | 9003-27-4 | sc-255434 | 100 g | $179.00 | ||
Polyisobutylene is a unique polymer known for its exceptional elasticity and low permeability to gases. Its structure features a branched configuration, which contributes to its viscoelastic properties and resistance to aging. The polymer exhibits strong intermolecular forces, enhancing its adhesive qualities. Additionally, its non-polar nature allows for compatibility with various hydrophobic materials, making it suitable for diverse applications in coatings and sealants. | ||||||