Ex 380-450 nm Violet

6,7-Dihydroxycoumarin-4-acetic Acid is a fluorescent compound that exhibits strong absorption and emission characteristics in the 380-450 nm range. Its dual hydroxyl groups enhance intramolecular hydrogen bonding, influencing its photostability and reactivity. The compound's unique structure facilitates specific interactions with metal ions, leading to potential coordination complexes. Additionally, its acidity can modulate reaction pathways, making it a fascinating subject for exploring molecular dynamics and environmental behavior.

GP-AMC is a fluorogenic substrate characterized by its remarkable fluorescence properties when excited in the 380-450 nm range. Its unique structure allows for selective interactions with various biomolecules, enhancing its sensitivity in detection applications. The compound's reactivity is influenced by its functional groups, which can participate in nucleophilic attacks, leading to distinct reaction kinetics. This behavior makes GP-AMC an intriguing candidate for studying molecular interactions and dynamics in diverse environments.

SBFI-AM is a fluorescent probe that exhibits exceptional sensitivity to changes in its microenvironment when excited within the 380-450 nm range. Its unique design facilitates specific binding interactions with target molecules, resulting in enhanced fluorescence intensity. The compound's acid halide functionality promotes rapid hydrolysis, influencing its reactivity and enabling dynamic studies of molecular interactions. This behavior underscores SBFI-AM's potential in exploring complex biochemical pathways.

8-Aminopyrene-1,3,6-trisulfonic acid trisodium salt is a highly fluorescent compound that exhibits remarkable photophysical properties when excited in the 380-450 nm range. Its sulfonic acid groups enhance solubility and ionic interactions, allowing for effective binding to various substrates. The compound's unique electronic structure facilitates energy transfer processes, making it a valuable tool for probing molecular dynamics and interactions in diverse environments.

Fluorogenic Proteasome Substrate is a specialized compound that exhibits strong fluorescence upon excitation in the 380-450 nm range. Its design incorporates specific peptide sequences that enable selective recognition and cleavage by proteasomes, leading to enhanced fluorescence. This substrate's unique structural features promote rapid reaction kinetics and facilitate real-time monitoring of proteolytic activity, providing insights into cellular processes and protein turnover dynamics.

Coumarin 30 is a fluorescent compound characterized by its unique ability to undergo intramolecular charge transfer, resulting in enhanced luminescence when excited within the 380-450 nm range. Its distinct molecular structure allows for specific interactions with various solvents, influencing its photophysical properties. The compound exhibits notable solvatochromism, where its emission spectrum shifts based on the polarity of the surrounding medium, making it a fascinating subject for studies on molecular dynamics and environmental sensing.

MPAC-Br is a halogenated compound that exhibits intriguing reactivity due to its electrophilic nature, facilitating nucleophilic substitution reactions. Its unique structure promotes strong dipole-dipole interactions, enhancing solubility in polar solvents. The compound's reactivity profile is influenced by steric factors, leading to distinct reaction kinetics. Additionally, MPAC-Br demonstrates notable photostability, making it suitable for studies involving light-induced processes and molecular interactions.

3-Morpholinobenzanthrone is a unique compound characterized by its planar structure, which enhances π-π stacking interactions, contributing to its solid-state properties. This compound exhibits significant fluorescence in the 380-450 nm range, making it a candidate for studies in photophysical behavior. Its electron-rich morpholine moiety facilitates hydrogen bonding, influencing solubility and reactivity in various environments. The compound's stability under UV light further supports its potential in photochemical applications.

4-(Trifluoromethyl)umbelliferyl phosphate disodium salt is distinguished by its strong electron-withdrawing trifluoromethyl group, which enhances its reactivity and alters its electronic properties. This compound exhibits notable fluorescence in the 380-450 nm range, attributed to its unique molecular structure that promotes efficient energy transfer. Its phosphate moiety facilitates interactions with various nucleophiles, influencing reaction kinetics and pathways in diverse chemical environments.

Aminostilbamidine methanesulfonate salt is characterized by its unique dual functional groups, which enable specific hydrogen bonding and ionic interactions. This compound exhibits significant fluorescence within the 380-450 nm range, driven by its conjugated system that stabilizes excited states. Its sulfonate group enhances solubility and reactivity, allowing for versatile interactions in various chemical contexts, influencing both reaction mechanisms and kinetics.