Photoreactive Crosslinkers

SDA (NHS-Diazirine) is a photoreactive crosslinker characterized by its diazirine group, which facilitates unique covalent bonding upon exposure to light. This compound exhibits rapid reaction kinetics, enabling efficient crosslinking through the formation of reactive carbene intermediates. Its distinct molecular structure enhances its ability to interact with diverse functional groups, promoting robust network formation. Additionally, SDA's stability under ambient conditions makes it suitable for various applications in material science.

LC-SDA (NHS-LC-Diazirine) is a versatile photoreactive crosslinker featuring a diazirine moiety that enables selective covalent attachment upon UV irradiation. Its unique reactivity profile allows for the generation of transient carbene species, which can engage in diverse molecular interactions. The compound's extended linker enhances spatial flexibility, facilitating targeted crosslinking in complex environments. Furthermore, LC-SDA's compatibility with various substrates promotes the formation of intricate polymer networks, making it a valuable tool in advanced material synthesis.

SDAD (NHS-SS-Diazirine) is a specialized photoreactive crosslinker characterized by its unique diazirine structure, which undergoes rapid photolysis upon UV exposure. This process generates highly reactive carbene intermediates, enabling efficient covalent bonding with nucleophiles. The presence of a disulfide linkage enhances its stability and allows for controlled release mechanisms. Additionally, SDAD's ability to form crosslinks in diverse chemical environments makes it an effective agent for creating complex, three-dimensional networks.

Sulfo-SDA (Sulfo-NHS-Diazirine) is a versatile photoreactive crosslinker distinguished by its diazirine moiety, which facilitates rapid formation of reactive carbene species upon UV irradiation. This reactivity allows for selective covalent attachment to various nucleophiles, promoting intricate molecular interactions. Its sulfonate group enhances solubility in aqueous environments, broadening its applicability. The compound's unique kinetics enable precise control over crosslinking dynamics, making it ideal for constructing tailored polymeric architectures.

Sulfo-LC-SDA (Sulfo-NHS-LC-Diazirine) is a specialized photoreactive crosslinker characterized by its ability to generate highly reactive carbene intermediates upon exposure to light. This property enables efficient and specific covalent bonding with a range of nucleophiles, facilitating complex molecular networks. The linker’s extended structure enhances flexibility and spatial arrangement, allowing for dynamic interactions in diverse environments. Its unique reactivity profile supports innovative approaches in material science and bioconjugation.

Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) is a versatile photoreactive crosslinker known for its unique disulfide bond, which provides stability and reversible linkage under specific conditions. Upon UV activation, it generates reactive diazirine species that readily engage with nucleophilic sites, enabling precise targeting in complex systems. Its hydrophilic nature enhances solubility in aqueous environments, promoting effective interactions in biological and synthetic matrices. This crosslinker’s distinct reactivity and structural features make it a powerful tool for creating intricate molecular architectures.

L-Photo-Leucine is a specialized photoreactive crosslinker characterized by its unique ability to form covalent bonds upon exposure to light. Its structure facilitates specific interactions with amino acids, allowing for selective crosslinking in diverse environments. The compound exhibits rapid reaction kinetics, enabling efficient formation of stable linkages. Additionally, its hydrophobic properties contribute to enhanced compatibility with various polymeric systems, making it ideal for creating complex networks in materials science.

L-Photo-Methionine is a distinctive photoreactive crosslinker known for its ability to engage in light-induced covalent bonding. Its sulfur-containing side chain enables unique interactions with thiol groups, promoting selective crosslinking in biomolecular assemblies. The compound demonstrates notable reaction kinetics, allowing for swift network formation. Furthermore, its amphiphilic nature enhances solubility in diverse solvents, facilitating integration into various polymer matrices for advanced material applications.

Benzophenone-4-carboxamidocysteine Methanethiosulfonate is a specialized photoreactive crosslinker that exhibits unique reactivity under UV light, enabling the formation of stable covalent bonds through its methanethiosulfonate moiety. This compound facilitates specific interactions with thiol groups, leading to tailored crosslinking in complex systems. Its distinct photochemical properties allow for controlled reaction kinetics, making it suitable for precise material engineering and structural modifications in various applications.

4-[3-(Trifluoromethyl)diazirin-3-yl]benzoic Acid N-Hydroxysuccinimide Ester is a versatile photoreactive crosslinker characterized by its diazirine moiety, which undergoes rapid cycloaddition upon UV irradiation. This compound exhibits high selectivity for nucleophiles, enabling efficient covalent bond formation with amines and other reactive groups. Its trifluoromethyl substitution enhances stability and solubility, while facilitating unique molecular interactions that allow for precise control over crosslinking dynamics in diverse experimental setups.