Items 91 to 100 of 141 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2,5-Diaminohydroquinone dihydrochloride | 24171-03-7 | sc-231066 | 1 g | $175.00 | ||
2,5-Diaminohydroquinone dihydrochloride is a distinctive polymer known for its rich amino and hydroquinone functionalities, which enable robust intermolecular interactions and facilitate electron transfer processes. Its unique structure promotes the formation of stable networks through hydrogen bonding and π-π stacking, enhancing its mechanical integrity. Additionally, the compound exhibits notable redox properties, allowing for dynamic reactivity in various environments, which can influence its stability and performance in polymeric applications. | ||||||
Hyaluronidase | 37259-53-3 | sc-360249 sc-360249A | 1 ampule 5 vial | $227.00 $865.00 | 4 | |
Hyaluronidase is an enzyme that catalyzes the hydrolysis of hyaluronic acid, breaking down its glycosidic bonds. This process alters the viscosity and elasticity of the surrounding matrix, facilitating the diffusion of other molecules. Its unique ability to interact with polysaccharides allows for modulation of tissue hydration and cellular signaling pathways. The enzyme's activity is influenced by pH and temperature, affecting its kinetic profile and efficiency in various environments. | ||||||
Colistin sodium methanesulfonate | 8068-28-8 | sc-252624 | 1 g | $147.00 | 1 | |
Colistin sodium methanesulfonate is a cationic peptide that exhibits unique interactions with bacterial membranes, disrupting lipid bilayers through electrostatic and hydrophobic forces. Its polymeric nature enhances its ability to form complexes with anionic molecules, influencing solubility and stability. The compound's behavior in aqueous solutions is characterized by its capacity to self-assemble, leading to the formation of micelle-like structures that can alter local microenvironments and enhance molecular interactions. | ||||||
Poly(methyl methacrylate) | 9011-14-7 | sc-255435 | 500 mg | $345.00 | 1 | |
Poly(methyl methacrylate) is a versatile polymer known for its exceptional optical clarity and resistance to UV degradation. Its amorphous structure allows for significant flexibility in processing, enabling various fabrication techniques. The polymer exhibits strong intermolecular forces, particularly van der Waals interactions, which contribute to its mechanical strength. Additionally, PMMA's glass transition behavior is crucial for applications requiring thermal stability, as it can maintain integrity under varying temperature conditions. | ||||||
1,4-Polyisoprene | 9003-31-0 | sc-253993 | 250 mg | $200.00 | ||
1,4-Polyisoprene is a natural rubber polymer characterized by its unique cis-1,4 configuration, which imparts remarkable elasticity and resilience. The polymer's long-chain structure facilitates extensive chain entanglement, enhancing its tensile strength and flexibility. Its ability to undergo crystallization under strain contributes to its dynamic mechanical properties. Additionally, 1,4-Polyisoprene exhibits excellent abrasion resistance and low hysteresis, making it suitable for various applications requiring durability and performance. | ||||||
O-(2-Aminoethyl)-O′-[2-(Boc-amino)ethyl]octaethylene glycol | 890091-43-7 | sc-236197 | 500 mg | $350.00 | ||
O-(2-Aminoethyl)-O'-[2-(Boc-amino)ethyl]octaethylene glycol is a multifunctional polymer distinguished by its Boc-protected amino groups, which provide stability and reactivity under specific conditions. The extensive octaethylene glycol backbone imparts significant hydrophilicity, enhancing its compatibility with aqueous environments. This polymer exhibits unique self-assembly properties, enabling the formation of micelles and nanostructures, while its amino groups facilitate diverse coupling reactions, expanding its utility in polymer chemistry. | ||||||
1-Amino-3,6,9-trioxaundecanyl-11-ol | 86770-74-3 | sc-208600 | 100 mg | $286.00 | ||
1-Amino-3,6,9-trioxaundecanyl-11-ol is a versatile polymer characterized by its unique ether and amine functionalities, which facilitate strong hydrogen bonding and enhance solubility in various solvents. Its linear structure promotes efficient chain alignment, resulting in improved mechanical strength and flexibility. The presence of multiple hydroxyl groups allows for extensive cross-linking potential, leading to enhanced thermal and chemical resistance. This polymer also exhibits interesting viscoelastic properties, making it suitable for diverse applications. | ||||||
Ammonium polyphosphate | 68333-79-9 | sc-492821 sc-492821A | 1 g 5 g | $189.00 $515.00 | ||
Ammonium polyphosphate is a versatile polymer characterized by its unique chain structure, which consists of varying lengths of phosphate units. This configuration allows for strong ionic interactions and hydrogen bonding, contributing to its thermal stability and flame-retardant properties. The polymer's ability to form cross-linked networks enhances its mechanical strength and resilience. Additionally, its hydrophilic nature facilitates moisture absorption, influencing its behavior in diverse applications. | ||||||
Polyisoprene, trans | 104389-32-4 | sc-493783 | 50 g | $140.00 | ||
Polyisoprene, trans, is a rubber-like polymer distinguished by its cis- and trans-configured double bonds, which influence its elasticity and tensile strength. The trans configuration enhances crystallinity, leading to improved mechanical properties and resistance to wear. Its unique molecular arrangement allows for effective chain entanglement, contributing to its viscoelastic behavior. Additionally, the polymer exhibits a high degree of resilience and flexibility, making it suitable for various dynamic applications. | ||||||
Isobutyl methacrylate | 97-86-9 | sc-250176 | 1 L | $65.00 | ||
Isobutyl methacrylate is a distinctive monomer that undergoes free radical polymerization, resulting in a flexible polymer with enhanced impact resistance. Its branched structure promotes steric hindrance, which influences the polymer's crystallinity and thermal properties. The presence of alkyl side groups enhances hydrophobic interactions, contributing to improved water resistance. Additionally, its reactivity allows for tailored copolymerization, enabling the design of materials with specific attributes for diverse applications. | ||||||