Items 131 to 140 of 141 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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alpha-Maleinimido-omega-carboxysuccinimidyl ester poly(ethyleneglycol), PEG molecular weight 5,000 daltons | sc-358040 | 100 mg | $430.00 | |||
Alpha-Maleinimido-omega-carboxysuccinimidyl ester poly(ethyleneglycol) is a specialized polymer distinguished by its reactive maleimide and succinimidyl ester functional groups, facilitating selective conjugation with thiol-containing molecules. This polymer exhibits enhanced stability and solubility due to its PEG backbone, promoting efficient molecular interactions. Its unique reactivity allows for controlled cross-linking and functionalization, making it ideal for creating complex polymer networks with tailored properties. | ||||||
Ethylene Terephthalate Cyclic Trimer | 7441-32-9 | sc-497588 sc-497588B sc-497588A | 1 mg 50 mg 5 mg | $246.00 $2511.00 $350.00 | 1 | |
Ethylene Terephthalate Cyclic Trimer is a cyclic oligomer that showcases unique molecular interactions, particularly through its ability to form hydrogen bonds and π-π stacking. This trimer exhibits distinct thermal and mechanical properties, contributing to its stability and rigidity. Its reactivity as a precursor in polymerization processes allows for controlled chain growth and tailored material characteristics, influencing the kinetics of polymer formation and the resulting polymer's morphology. | ||||||
Polyglycolide | 26124-68-5 | sc-506517 | 5 g | $559.00 | ||
Polyglycolide is a biodegradable polymer characterized by its unique chain structure, which allows for significant intermolecular hydrogen bonding. This property enhances its mechanical strength and thermal stability. The polymer undergoes hydrolytic degradation, leading to a predictable release of degradation products. Its crystalline nature influences the rate of degradation, making it suitable for controlled applications. The polymer's ability to form blends with other materials further expands its versatility in various environments. | ||||||
Hydrogenated bisphenol A | 80-04-6 | sc-353624 sc-353624A sc-353624B | 1 g 5 g 25 g | $31.00 $61.00 $143.00 | ||
Hydrogenated bisphenol A is a unique polymer precursor known for its enhanced thermal stability and mechanical strength. Its structure features multiple hydroxyl groups that facilitate hydrogen bonding, promoting strong intermolecular interactions. This results in improved resistance to chemical degradation and environmental stress. The compound's ability to undergo cross-linking reactions contributes to the formation of robust, durable materials, making it suitable for high-performance applications. | ||||||
Pentaerythritol Tetra(3-mercaptopropionate) | 7575-23-7 | sc-485372 sc-485372A | 100 ml 500 ml | $53.00 $132.00 | ||
Pentaerythritol Tetra(3-mercaptopropionate) is a multifunctional thiol compound that exhibits unique cross-linking capabilities in polymer chemistry. Its four mercaptopropionate groups enable rapid thiol-ene reactions, facilitating the formation of robust networks. The compound's high reactivity with unsaturated compounds enhances its utility in creating diverse polymer architectures. Additionally, its ability to form strong disulfide bonds contributes to the thermal and mechanical stability of the resulting materials. | ||||||
2-Hydroxy-2-methylpropiophenone | 7473-98-5 | sc-486642 sc-486642A | 50 ml 250 ml | $67.00 $214.00 | ||
2-Hydroxy-2-methylpropiophenone is a versatile photoinitiator in polymer chemistry, facilitating the curing process of various resins through radical generation upon UV exposure. Its unique structure allows for efficient absorption of light, leading to rapid polymerization kinetics. The compound's ability to form stable radicals enhances cross-linking in polymer networks, resulting in materials with improved mechanical properties and thermal stability. Its reactivity can be finely tuned, enabling tailored applications in advanced polymer formulations. | ||||||
FITC-Dextran 4 | 60842-46-8 | sc-507149 sc-507149A | 100 mg 500 mg | $173.00 $349.00 | ||
FITC-Dextran 4 is a versatile polymer characterized by its dextran structure conjugated with fluorescein isothiocyanate. This compound exhibits unique solubility properties and a high degree of hydration, which influence its diffusion rates in various media. Its branched architecture allows for multiple sites of interaction, enhancing its capacity for complex formation with biomolecules. Additionally, the fluorescence properties can be modulated by pH changes, providing insights into microenvironmental conditions. | ||||||
Polyethyleneimine, linear, M.W. 25,000 | 9002-98-6 | sc-507213 | 250 mg | $959.00 | 2 | |
Linear Polyethyleneimine with a molecular weight of 25,000 exhibits a unique combination of high charge density and flexible chain conformation, facilitating effective ion exchange and complexation with various anions. Its hydrophilic nature enhances compatibility with aqueous systems, while the presence of primary, secondary, and tertiary amines allows for diverse functionalization. This polymer's ability to form stable colloidal dispersions and gels under specific conditions highlights its potential in advanced material formulations. | ||||||
Poly(deoxyinosinic-deoxycytidylic) acid sodium salt | 118578-37-3 | sc-286691 sc-286691A sc-286691B | 5 units 10 units 25 units | $180.00 $285.00 $560.00 | 2 | |
Poly(deoxyinosinic-deoxycytidylic) acid sodium salt is a unique polymer characterized by its double-stranded helical structure, which promotes specific molecular interactions through hydrogen bonding and base stacking. This polymer exhibits significant stability in physiological conditions, enabling it to engage in distinct pathways of cellular recognition. Its high viscosity and gel-forming capabilities enhance its physical properties, allowing for effective manipulation in various environments. The polymer's ability to form complexes with cationic agents further underscores its versatility in diverse applications. | ||||||
O-(2-Aminoethyl)polyethylene glycol 3,000 | 32130-27-1 | sc-228847 | 250 mg | $214.00 | ||
O-(2-Aminoethyl)polyethylene glycol 3,000 is a versatile polymer distinguished by its hydrophilic nature and ability to form hydrogen bonds, enhancing solubility in aqueous environments. Its branched structure facilitates unique molecular interactions, promoting stability and flexibility. The polymer exhibits low toxicity and biocompatibility, allowing for tailored modifications that can influence reaction kinetics and enhance its performance in various chemical processes. Its ability to form hydrogels further expands its functional applications. |