Items 71 to 80 of 141 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Poly(2-vinylpyridine) | 25014-15-7 | sc-255430 | 1 g | $59.00 | ||
Poly(2-vinylpyridine) is a versatile polymer known for its strong hydrogen bonding capabilities due to the presence of pyridine rings. This feature enhances its solubility in polar solvents and facilitates complexation with metal ions. The polymer exhibits a unique ability to undergo protonation, leading to changes in its physical properties, such as increased conductivity. Its structural rigidity and thermal stability make it suitable for applications requiring durable materials with specific interaction profiles. | ||||||
Allyl ether | 557-40-4 | sc-397470 | 25 g | $130.00 | ||
Allyl ether is a reactive compound that participates in polymerization through its double bond, enabling the formation of cross-linked networks. Its unique structure allows for efficient radical polymerization, resulting in materials with enhanced flexibility and resilience. The presence of ether linkages contributes to its compatibility with various solvents, while its ability to undergo chain transfer reactions can influence molecular weight distribution. This behavior is crucial for tailoring polymer properties in diverse applications. | ||||||
Poly(vinylpolypyrrolidone) | 25249-54-1 | sc-253293 sc-253293A | 25 g 100 g | $46.00 $77.00 | ||
Poly(vinylpolypyrrolidone) is a versatile polymer characterized by its high affinity for moisture and ability to form hydrogen bonds, which enhances its solubility in various solvents. Its unique structure allows for strong intermolecular interactions, leading to increased viscosity and film-forming capabilities. The polymer exhibits a distinct ability to stabilize emulsions and dispersions, making it an effective thickening agent. Additionally, its molecular weight can be finely tuned, influencing its rheological properties and performance in diverse environments. | ||||||
Poly(dimethylsiloxane) | 9016-00-6 | sc-253289 | 100 g | $56.00 | ||
Poly(dimethylsiloxane) is a silicone-based polymer known for its exceptional flexibility and low surface tension, which facilitates unique interactions with various substrates. Its linear structure allows for a wide range of molecular weights, influencing its viscosity and mechanical properties. The polymer exhibits remarkable thermal stability and hydrophobicity, making it resistant to environmental degradation. Additionally, its ability to form siloxane bonds contributes to its elasticity and resilience, enabling diverse applications in coatings and sealants. | ||||||
Paraformaldehyde | 30525-89-4 | sc-253236 sc-253236B sc-253236A | 25 g 500 g 100 g | $35.00 $47.00 $41.00 | 173 | |
Paraformaldehyde is a formaldehyde polymer that exhibits unique properties due to its cyclic structure, facilitating cross-linking in polymer networks. Its high reactivity allows for rapid polymerization, leading to the formation of thermosetting resins. The presence of hydroxymethyl groups enhances hydrogen bonding, which significantly influences the mechanical strength and thermal stability of the resulting materials. Additionally, its crystalline nature contributes to improved rigidity and dimensional consistency in various polymer applications. | ||||||
3,6-Dichlorophthalic anhydride | 4466-59-5 | sc-396781 sc-396781A | 1 g 5 g | $178.00 $300.00 | ||
3,6-Dichlorophthalic anhydride is a versatile compound that serves as a key building block in polymer chemistry. Its anhydride functionality enables efficient acylation reactions, promoting the formation of polyesters and polyamides through condensation polymerization. The presence of chlorine atoms enhances reactivity and introduces unique dipole interactions, influencing the thermal and mechanical properties of the resulting polymers. This compound's rigid aromatic structure contributes to high glass transition temperatures, providing dimensional stability in various applications. | ||||||
Tyloxapol | 25301-02-4 | sc-255711 sc-255711A sc-255711B | 5 g 10 g 50 g | $82.00 $112.00 $362.00 | 1 | |
Tyloxapol is a nonionic surfactant characterized by its unique amphiphilic structure, which promotes effective stabilization of emulsions and foams. Its polymeric nature allows for versatile interactions with both hydrophilic and hydrophobic substances, enhancing solubilization and dispersion. The presence of ethylene oxide units contributes to its low surface tension and excellent wetting properties, making it suitable for applications that require efficient surface activity and enhanced compatibility with various formulations. | ||||||
DEAE Dextran | 9015-73-0 | sc-358753B sc-358753A sc-358753 | 5 g 100 g 25 g | $52.00 $417.00 $145.00 | ||
DEAE Dextran is a branched polysaccharide known for its high molecular weight and unique ability to form hydrogels. Its structure facilitates strong hydrogen bonding and electrostatic interactions, allowing it to effectively modulate viscosity and enhance stability in various environments. The polymer exhibits remarkable biocompatibility and can undergo controlled degradation, making it suitable for diverse applications that require tailored physical properties and responsive behavior in solution. | ||||||
Poly-L-Aspartic Acid Sodium Salt | 31871-95-1 | sc-296108 sc-296108A | 10 mg 50 mg | $98.00 $169.00 | ||
Poly-L-Aspartic Acid Sodium Salt is a versatile polymer characterized by its anionic nature and ability to form stable complexes with cationic species. Its unique structure promotes strong ionic interactions and hydrogen bonding, leading to enhanced solubility and viscosity modulation in aqueous environments. The polymer's chain flexibility and hydrophilicity contribute to its capacity for water retention and film-forming properties, making it suitable for various applications requiring tailored rheological behavior. | ||||||
1,1′-Azobis(cyclohexanecarbonitrile) | 2094-98-6 | sc-237651 | 25 g | $61.00 | ||
1,1'-Azobis(cyclohexanecarbonitrile) is a versatile azo compound that serves as a radical initiator in polymerization processes. Its unique structure allows for efficient homolytic cleavage, generating free radicals that initiate chain reactions. The compound exhibits distinct thermal stability, enabling controlled polymer growth and influencing molecular weight distribution. Additionally, its ability to participate in cross-linking reactions enhances the mechanical properties of resulting polymers, making them suitable for diverse applications. |