Em 590-620 nm Orange

Tetramethylrhodamine ethyl ester perchlorate is a highly fluorescent dye characterized by its emission spectrum in the 590-620 nm range. Its unique structure promotes efficient energy transfer and strong Stokes shift, resulting in vivid fluorescence. The compound's interactions with surrounding media can lead to notable changes in its photophysical properties, including quenching effects in different environments. Its robust stability under various conditions makes it a fascinating subject for exploring light-matter interactions.

Chromeo™ P503 is an innovative chemical exhibiting remarkable photophysical properties, particularly in the 590-620 nm emission range. Its unique molecular architecture facilitates specific interactions with surrounding solvents, enhancing its fluorescence intensity. The compound demonstrates distinct reaction kinetics, allowing for rapid energy transfer processes. Additionally, its stability across diverse conditions makes it an intriguing candidate for studying dynamic molecular behaviors and environmental influences on fluorescence.

Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride complex showcases exceptional luminescent characteristics, particularly emitting light in the 590-620 nm range. Its intricate coordination sphere promotes strong π-π stacking interactions, leading to enhanced photostability. The complex exhibits unique electron transfer dynamics, facilitating efficient energy migration. Its robust structural integrity under varying conditions allows for in-depth exploration of photochemical pathways and molecular interactions in diverse environments.

Sulforhodamine 101 acid chloride is a vibrant dye characterized by its strong absorption and emission properties in the 590-620 nm range. As an acid halide, it exhibits high reactivity, particularly in acylation reactions, where it readily forms stable amides. The presence of the sulfonyl group enhances solubility in polar solvents, promoting unique molecular interactions. Its distinct electronic structure allows for efficient energy transfer, making it a subject of interest in photophysical studies.

5(6)-Carboxy-X-rhodamine N-succinimidyl ester is a fluorescent dye notable for its robust emission in the 590-620 nm range. This compound features a reactive N-succinimidyl ester moiety, facilitating selective labeling through nucleophilic attack by amines. Its carboxyl group enhances solubility and stability in aqueous environments, while the conjugated system contributes to its photostability and efficient light absorption, making it suitable for various analytical applications.

Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) bis(hexafluorophosphate) complex exhibits remarkable luminescent properties, emitting light in the 590-620 nm range. This complex showcases strong metal-ligand interactions, enhancing its stability and photophysical characteristics. The unique arrangement of phenanthroline ligands facilitates efficient energy transfer and electron delocalization, resulting in prolonged excited-state lifetimes and distinct photochemical pathways, making it a subject of interest in advanced material studies.

3-(2-Furoyl)quinoline-2-carboxaldehyde is a compound that exhibits intriguing photophysical behavior, particularly in the 590-620 nm emission range. Its structure allows for significant intramolecular hydrogen bonding, which influences its electronic properties and enhances its fluorescence. The presence of the furoyl group contributes to unique charge transfer dynamics, facilitating rapid excited-state relaxation and distinct photochemical reactivity, making it a fascinating subject for studies in luminescent materials.

Sulforhodamine 101 DHPE is a vibrant dye characterized by its strong emission in the 590-620 nm range. Its unique structure promotes effective π-π stacking interactions, enhancing its stability and fluorescence intensity. The compound exhibits notable solvatochromism, where its emission properties shift based on the solvent environment, revealing insights into molecular interactions. Additionally, its robust photostability makes it suitable for various applications in fluorescence-based studies.

Texas Red-2-sulfonamidoethyl methanethiosulfonate is a fluorescent compound that exhibits a striking emission in the 590-620 nm range. Its distinctive sulfonamide group facilitates specific interactions with biomolecules, enhancing its utility in probing cellular environments. The compound's reactivity with thiols allows for selective labeling, while its unique electronic structure contributes to a high quantum yield. This dye's exceptional photostability and sensitivity to environmental changes make it a powerful tool for studying dynamic processes.

Texas Red-2-Sulfonamidoethyl Mercaptan is a vibrant fluorescent dye characterized by its emission spectrum in the 590-620 nm range. Its sulfonamidoethyl moiety enhances solubility and promotes specific interactions with various substrates. The compound's unique reactivity profile allows for efficient conjugation with thiol groups, facilitating targeted labeling. Additionally, its robust photophysical properties, including high extinction coefficients and stability under diverse conditions, make it ideal for detailed fluorescence studies.