Em 380-450 nm Violet

9-Maleimidoacridine is a fluorescent compound that emits light in the 380-450 nm range, distinguished by its acridine backbone and maleimide functionality. This compound exhibits strong reactivity towards thiol groups, facilitating the formation of stable thioether linkages. Its unique electronic structure allows for efficient energy transfer processes, enhancing fluorescence under specific conditions. Additionally, the compound's solubility in organic solvents broadens its applicability in diverse chemical environments, making it a versatile tool for probing molecular interactions.

9-Aminoacridine hydrochloride is a fluorescent compound characterized by its acridine core, which enables emission in the 380-450 nm range. Its amino group enhances hydrogen bonding and facilitates interactions with various biomolecules, influencing reaction kinetics. The compound's planar structure promotes stacking interactions, potentially affecting its aggregation behavior. Additionally, its solubility in polar solvents allows for diverse applications in studying molecular dynamics and interactions.

7-Methoxycoumarin-4-acetic Acid exhibits fluorescence in the 380-450 nm range, attributed to its unique coumarin backbone. The methoxy group enhances electron donation, influencing its photophysical properties and reactivity. This compound can engage in intramolecular hydrogen bonding, affecting its conformational stability. Its ability to participate in various chemical reactions, including esterification and acylation, highlights its versatility in synthetic pathways. Additionally, its solubility in organic solvents facilitates diverse interactions in complex systems.

6,7-Dimethoxycoumarin-4-acetic Acid displays notable fluorescence within the 380-450 nm spectrum, stemming from its distinctive coumarin structure. The presence of two methoxy groups significantly alters its electronic distribution, enhancing its reactivity and interaction with light. This compound can form stable complexes through π-π stacking and hydrogen bonding, influencing its behavior in various environments. Its high solubility in polar solvents allows for effective participation in diverse chemical transformations, showcasing its adaptability in synthetic chemistry.

7-Amino-4-methyl-3-coumarinylacetic acid exhibits remarkable fluorescence in the 380-450 nm range, attributed to its unique coumarin framework. The amino group enhances its hydrogen bonding capabilities, facilitating strong interactions with polar solvents. This compound's structural features promote efficient energy transfer and photostability, making it an intriguing candidate for studying molecular dynamics. Its reactivity is further influenced by the methyl substituent, which modulates steric effects and electronic properties.

INDO 1/AM is a fluorescent probe characterized by its distinct emission properties in the 380-450 nm range, stemming from its unique indole structure. The compound's ability to chelate metal ions enhances its photophysical behavior, leading to increased fluorescence intensity. Its hydrophobic regions promote membrane permeability, while the presence of functional groups allows for specific interactions with biological macromolecules, influencing reaction kinetics and molecular recognition processes.

7-Amino-4-methyl-3-coumarinacetic acid N-succinimidyl ester exhibits notable fluorescence in the 380-450 nm range, attributed to its coumarin backbone. This compound features a reactive N-succinimidyl ester group, facilitating efficient conjugation with amines, which enhances its utility in labeling applications. Its unique structural attributes promote strong intramolecular interactions, influencing stability and reactivity, while its solubility characteristics allow for versatile applications in various environments.

7-Ethoxy-4-(trifluoromethyl)coumarin displays remarkable fluorescence within the 380-450 nm range, driven by its distinctive coumarin structure. The trifluoromethyl group enhances electron-withdrawing properties, significantly affecting its photophysical behavior and reactivity. This compound exhibits unique solvent-dependent fluorescence shifts, indicative of specific molecular interactions. Its ethoxy substituent contributes to solubility, enabling diverse applications in various chemical environments.

7-HC-γ-linolenate exhibits intriguing photophysical properties, particularly in the 380-450 nm range, due to its unique unsaturated fatty acid structure. The presence of multiple double bonds facilitates distinct electron delocalization, enhancing its light absorption characteristics. This compound demonstrates notable reactivity in lipid peroxidation pathways, influencing its interaction with biological membranes. Its hydrophobic nature allows for specific molecular interactions, impacting its behavior in various environments.

7-Methoxycoumarin-4-acetic Acid N-Succinimidyl Ester is characterized by its distinctive fluorescence properties within the 380-450 nm range, attributed to the coumarin moiety's conjugated system. This compound exhibits a propensity for nucleophilic attack due to the electrophilic nature of the succinimidyl ester, facilitating selective coupling reactions. Its solubility in organic solvents enhances its reactivity, allowing for efficient interactions in diverse chemical environments.