Em 450-495 nm Blue

Bis(1-pyrenylmethyl) Ether exhibits remarkable photophysical properties, particularly in the 450-495 nm emission range. Its pyrene moieties contribute to strong π-π stacking interactions, enhancing its luminescence. The compound's unique structure allows for efficient intramolecular energy transfer, leading to pronounced fluorescence. Additionally, its ability to engage in non-covalent interactions, such as van der Waals forces, influences its solubility and reactivity in diverse environments, showcasing its dynamic behavior in various media.

10-(3-Sulfopropyl)acridinium betaine is characterized by its distinctive emission properties within the 450-495 nm range, attributed to its acridinium core. The presence of the sulfopropyl group enhances solubility in aqueous environments, facilitating unique ionic interactions. This compound exhibits rapid electron transfer kinetics, making it a potent candidate for studies involving photochemical reactions. Its structural design promotes effective charge separation, contributing to its luminescent efficiency and reactivity in diverse chemical contexts.

Indo 1 is notable for its exceptional fluorescence characteristics, particularly within the 450-495 nm spectrum. Its unique structure allows for strong dipole-dipole interactions, enhancing its photostability. The compound exhibits rapid energy transfer processes, which are crucial for its role in various photophysical studies. Additionally, Indo 1's ability to form stable complexes with metal ions can influence its reactivity and emission properties, making it a versatile tool in chemical research.

Atto 425-NHS ester is distinguished by its efficient coupling reactivity, particularly in the formation of stable amide bonds. This compound exhibits a high degree of specificity in labeling biomolecules, facilitated by its reactive NHS ester group. Its fluorescence properties are enhanced by a unique electron-withdrawing structure, which stabilizes the excited state and promotes efficient energy transfer. The compound's solubility in various solvents further supports diverse experimental applications.

7-Diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin is characterized by its remarkable fluorescence emission in the 450-495 nm range, attributed to its unique coumarin backbone. The presence of the maleimide moiety allows for selective thiol-reactive labeling, enhancing its utility in bioconjugation. Its electron-rich diethylamino group contributes to a strong Stokes shift, improving signal clarity in complex environments. Additionally, the compound exhibits favorable solubility in polar solvents, facilitating diverse experimental conditions.

Hoechst 34580 is distinguished by its strong fluorescence emission within the 450-495 nm range, stemming from its unique structural features. The compound's ability to intercalate into DNA is facilitated by its planar aromatic system, promoting specific molecular interactions with nucleic acids. This intercalation enhances its photostability and allows for effective visualization in various environments. Its high quantum yield and distinct spectral properties make it suitable for advanced imaging applications.

Dibromobimane exhibits remarkable fluorescence in the 450-495 nm range, attributed to its unique dibrominated structure that enhances electron delocalization. This compound engages in specific interactions with thiol groups, leading to selective labeling in biochemical assays. Its rapid reaction kinetics with biomolecules allow for real-time monitoring, while its robust photophysical properties ensure stability under varied conditions, making it a versatile tool in fluorescence studies.

EDANS C2 maleimide is a fluorescent probe that emits light in the 450-495 nm range, characterized by its maleimide moiety which facilitates selective conjugation with thiol-containing compounds. This compound exhibits a high degree of photostability and a favorable quantum yield, enabling efficient energy transfer in various environments. Its unique reactivity profile allows for precise labeling, making it an effective choice for studying molecular interactions and dynamics in complex systems.

EDANS iodoacetamide is a fluorescent labeling agent that operates effectively within the 450-495 nm emission spectrum. Its iodoacetamide group enables robust covalent bonding with nucleophilic sites, particularly thiols, enhancing specificity in biomolecular studies. The compound's unique electronic structure contributes to its strong fluorescence and stability under various conditions, facilitating detailed investigations into protein conformations and interactions. Its rapid reaction kinetics further support dynamic studies in complex biological systems.

Suc-Leu-Leu-Val-Tyr-AMC is a fluorescent substrate that emits light in the 450-495 nm range, characterized by its peptide structure which allows for selective cleavage by specific proteases. The compound's unique sequence promotes interactions with enzyme active sites, enhancing substrate specificity. Its hydrophobic regions contribute to solubility and stability in diverse environments, while the amide bond facilitates rapid enzymatic hydrolysis, making it a valuable tool for studying proteolytic activity.