General Crosslinkers
Items 341 to 344 of 344 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
3-[2-N-(Biotinyl)aminoethyldithio]propanoic Acid | 104582-29-8 | sc-206612A sc-206612B sc-206612 | 10 mg 50 mg 100 mg | $148.00 $235.00 $367.00 | ||
3-[2-N-(Biotinyl)aminoethyldithio]propanoic Acid serves as an effective crosslinker, facilitating the formation of stable covalent bonds between biomolecules. Its unique dithioether functionality allows for selective thiol-disulfide exchange reactions, enhancing the stability of conjugated structures. The biotinyl group promotes strong affinity for streptavidin, enabling targeted assembly in complex biochemical systems. This compound's reactivity and specificity make it a versatile tool for creating intricate molecular networks. | ||||||
Butyl 3-mercaptopropionate | 16215-21-7 | sc-396842 | 100 ml | $37.00 | ||
Butyl 3-mercaptopropionate serves as an effective crosslinker due to its thiol functional group, which readily engages in nucleophilic reactions with electrophilic sites in polymers. This compound's unique ability to form disulfide bonds enhances network stability and mechanical properties. Its flexible alkyl chain contributes to the overall elasticity of the resulting materials, while the presence of the mercapto group facilitates rapid reaction kinetics, promoting efficient crosslinking in various polymer matrices. | ||||||
N-Propyldiethanolamine | 6735-35-9 | sc-476852 | 1 g | $380.00 | ||
N-Propyldiethanolamine serves as an effective crosslinker due to its multifunctional amine and alcohol groups, which facilitate robust network formation in polymer matrices. Its unique ability to engage in hydrogen bonding enhances adhesion and mechanical strength. The compound's steric configuration allows for tailored reactivity, enabling selective crosslinking pathways that optimize curing processes. Additionally, its hydrophilic nature influences compatibility with various substrates, enhancing overall performance in composite materials. | ||||||
4-Azidotetrafluorobenzaldehyde | 120384-18-1 | sc-503200 | 250 mg | $380.00 | ||
4-Azidotetrafluorobenzaldehyde is a highly reactive crosslinker known for its unique azide functional group, which facilitates click chemistry reactions. Its tetrafluorinated structure enhances electron-withdrawing properties, promoting rapid nucleophilic attack in polymer networks. The compound's distinct reactivity allows for selective bonding in diverse environments, leading to tailored material properties. Additionally, its stability under various conditions makes it suitable for intricate crosslinking applications. | ||||||