Other Crosslinkers

2-[2-[2-[2-[6-(Biotinylaminohexanoyl]aminoethoxy]ethoxy]ethoxy]-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid serves as a sophisticated crosslinker, characterized by its unique trifluoromethyl and diazirine functionalities. These features enable photochemical activation, allowing for selective covalent bond formation under UV light. The biotinyl group enhances biocompatibility, while the ethoxy linkers provide flexibility, facilitating intricate molecular interactions and enhancing network formation in complex systems.

1,17-Bisbiotinylamino-3,6,9,12,15-pentaoxaheptadecane is a versatile crosslinker distinguished by its extended polyether backbone and dual biotinyl groups. This structure promotes robust molecular interactions through multiple hydrogen bonding sites, enhancing stability in polymer networks. The unique arrangement of ether linkages contributes to its solubility and flexibility, allowing for dynamic crosslinking pathways that can adapt to varying environmental conditions, optimizing network integrity.

3-[(2-Aminoethyl)dithio]propionic Acid serves as a distinctive crosslinker characterized by its dithioether functionality, which facilitates the formation of disulfide bonds. This property enables the creation of stable, covalent linkages in polymer matrices, enhancing mechanical strength and resilience. The presence of amino groups allows for additional ionic interactions, promoting further network complexity. Its unique reactivity and ability to undergo thiol-disulfide exchange reactions provide dynamic crosslinking capabilities, adapting to diverse conditions.

N-Biotinylcaproylaminocaproic Acid is a versatile crosslinker distinguished by its biotinylated structure, which enhances molecular recognition through specific binding interactions. Its amine and carboxylic acid groups facilitate robust covalent bonding, promoting the formation of intricate polymer networks. The unique spatial arrangement of its functional groups allows for selective reactivity, enabling tailored modifications and dynamic crosslinking under varying conditions, thus enhancing material properties.

Angelicin is a distinctive crosslinker characterized by its ability to engage in specific π-π stacking interactions due to its aromatic structure. This property allows for enhanced stability in polymer matrices. Its reactivity is influenced by the presence of multiple functional groups, which can facilitate diverse bonding mechanisms, including covalent and non-covalent interactions. The compound's unique conformational flexibility contributes to its effectiveness in forming complex, resilient networks under various environmental conditions.

Biotinyl Cystamine is a versatile crosslinker known for its ability to form disulfide bonds, which provide dynamic stability in polymer systems. Its unique structure allows for selective interactions with thiol groups, promoting tailored crosslinking pathways. The compound exhibits a high degree of solubility in various solvents, enhancing its compatibility with different matrices. Additionally, its reactivity is modulated by environmental factors, enabling controlled network formation.

Deoxypyridinoline Chloride Trihydrochloride Salt serves as a distinctive crosslinker, characterized by its ability to engage in specific interactions with collagen and other proteins. This compound facilitates the formation of stable crosslinked networks through unique ionic and hydrogen bonding mechanisms. Its solubility in aqueous environments enhances its integration into diverse biological matrices, while its reactivity can be finely tuned by pH variations, allowing for precise control over crosslinking dynamics.

2-[Nα-Benzoylbenzoicamido-N6-(6-biotinamidocaproyl)-L-lysinylamido]ethyl Methanethiosulfonate acts as a versatile crosslinker, notable for its ability to form covalent bonds through thiol-disulfide exchange reactions. This compound exhibits selective reactivity with thiol groups, enabling the formation of stable linkages in complex biomolecular systems. Its unique structure allows for specific targeting of functional groups, enhancing the precision of crosslinking in various applications.

Cyclophosphamide-d4 serves as a distinctive crosslinker, characterized by its ability to engage in nucleophilic substitution reactions. This compound features a unique phosphoramide moiety that facilitates the formation of stable covalent bonds with nucleophiles, particularly amines and thiols. Its isotopic labeling enhances tracking in complex biochemical pathways, providing insights into reaction kinetics and molecular interactions. The compound's reactivity profile allows for tailored crosslinking strategies in diverse experimental contexts.

N-Fmoc-N"-succinyl-4,7,10-trioxa-1,13-tridecanediamine is a versatile crosslinker known for its ability to form robust networks through multiple functional groups. Its unique structure promotes hydrogen bonding and hydrophobic interactions, enhancing stability in various environments. The presence of the Fmoc group allows for selective deprotection, enabling controlled release and functionalization. This compound's reactivity is influenced by its chain length and flexibility, facilitating diverse crosslinking applications.