Ex 495-570 nm Green

Tetramethylrhodamine isothiocyanate Isomer R is a vibrant fluorescent dye that exhibits remarkable stability and photostability, making it ideal for various experimental conditions. Its unique isothiocyanate group enables efficient covalent bonding with amine-containing biomolecules, facilitating targeted labeling. The compound's fluorescence intensity is highly responsive to local microenvironments, allowing for detailed studies of molecular interactions and dynamics in complex biological systems.

5(6)-Carboxy-2',7'-dichlorofluorescein is a fluorescent compound characterized by its strong emission in the 495-570 nm range. Its carboxylic acid group enhances solubility in aqueous environments, promoting effective interaction with various biomolecules. The dichlorofluorescein structure allows for pH-dependent fluorescence, enabling the monitoring of changes in local acidity. This compound's unique photophysical properties make it suitable for probing dynamic processes in diverse experimental settings.

Rhodamine 101 Inner Salt is a vibrant fluorescent dye exhibiting strong emission in the 495-570 nm range. Its unique structure features a positively charged nitrogen, enhancing its affinity for anionic species and facilitating specific molecular interactions. This compound demonstrates remarkable photostability and high quantum yield, making it ideal for applications requiring consistent fluorescence. Additionally, its ability to undergo protonation and deprotonation under varying pH conditions allows for versatile use in studying environmental changes.

FLUO 3, Pentaammonium Salt, is a distinctive fluorescent compound characterized by its intense emission in the 495-570 nm spectrum. Its unique pentaammonium structure promotes strong ionic interactions, enhancing solubility in polar solvents. The compound exhibits exceptional stability under light exposure, with a high extinction coefficient that contributes to its intense fluorescence. Its reactivity with various anions allows for dynamic behavior in diverse chemical environments, making it a subject of interest in studies of molecular interactions.

Rhodamine B octadecyl ester perchlorate is a vibrant fluorescent dye that exhibits strong emission in the 495-570 nm range. Its unique octadecyl ester modification enhances hydrophobic interactions, promoting aggregation in non-polar environments. This compound demonstrates remarkable photostability and a high quantum yield, making it suitable for various analytical applications. Its ability to form complexes with metal ions further enriches its chemical behavior, allowing for diverse explorations in fluorescence studies.

NHS-5(6)Carboxyrhodamine is a fluorescent dye characterized by its intense emission spectrum between 495-570 nm. This compound features a carboxyl group that facilitates strong hydrogen bonding and enhances solubility in polar solvents. Its unique structure allows for efficient energy transfer and photophysical properties, including high molar absorptivity. Additionally, it can participate in specific interactions with biomolecules, making it a versatile tool for studying molecular dynamics and interactions.

Tetramethylrhodamine-5-maleimide is a vibrant fluorescent dye exhibiting a strong emission range of 495-570 nm. Its maleimide group enables selective conjugation with thiol-containing compounds, facilitating targeted labeling in various biochemical applications. The compound's rigid structure enhances photostability and minimizes non-radiative decay, resulting in prolonged fluorescence. Its unique electronic properties allow for efficient Förster resonance energy transfer, making it ideal for probing molecular interactions.

Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) bis(perchlorate) is a luminescent complex characterized by its robust photophysical properties, particularly in the 495-570 nm range. The intricate π-π stacking interactions between the phenanthroline ligands enhance its stability and luminescence efficiency. This compound exhibits unique redox behavior, allowing for versatile electron transfer pathways, which can be influenced by solvent polarity and temperature, making it a subject of interest in photochemical studies.

CruzFluor sm™ 2 amine is a specialized chemical exhibiting remarkable fluorescence properties within the 495-570 nm spectrum. Its unique structure facilitates strong hydrogen bonding and dipole-dipole interactions, enhancing its photostability. The compound's reactivity as an acid halide allows for selective nucleophilic attack, leading to distinct reaction kinetics. Additionally, its solubility in various solvents influences its emission characteristics, making it a fascinating subject for photophysical research.

CruzQuench™ 2WS acid is a distinctive compound characterized by its ability to modulate fluorescence in the 495-570 nm range. Its unique molecular architecture promotes specific interactions with nearby polar molecules, influencing its quenching efficiency. The acid halide functionality enables rapid acylation reactions, showcasing notable kinetics. Furthermore, its solubility profile in diverse media alters its spectral behavior, making it an intriguing candidate for studies in photochemical dynamics.