Em 620-750 nm Red

3,3'-Diethylthiadicarbocyanine iodide is a fluorescent dye notable for its emission spectrum spanning 620-750 nm. This compound exhibits strong intermolecular interactions due to its extended conjugated system, which enhances its light-absorbing properties. Its unique charge distribution allows for effective energy transfer processes, making it suitable for various photophysical applications. The dye's hydrophobic nature influences its aggregation behavior, impacting its optical characteristics in different media.

3-Morpholinobenzanthrone is a compound characterized by its emission in the 620-750 nm range, attributed to its robust π-conjugated system. This structure facilitates unique electronic transitions, leading to pronounced photostability and efficient light absorption. The presence of the morpholine group enhances solubility and alters the compound's reactivity, influencing its interaction with various substrates. Its distinct molecular geometry contributes to selective binding and unique photophysical properties, making it a subject of interest in advanced material studies.

CruzFluor sm™ 5 acid exhibits remarkable fluorescence in the 620-750 nm spectrum, driven by its intricate electronic structure. The compound's unique acid halide characteristics promote rapid acylation reactions, enhancing its reactivity with nucleophiles. Its tailored steric environment allows for selective interactions, influencing reaction kinetics and pathways. Additionally, the compound's stability under various conditions makes it a fascinating subject for exploring molecular dynamics and photochemical behavior.

CruzFluor sm™ 5 maleimide showcases exceptional photophysical properties, emitting fluorescence within the 620-750 nm range. Its unique maleimide functionality facilitates specific thiol-reactive interactions, leading to selective conjugation with biomolecules. The compound's rigid structure enhances its photostability, while its electronic configuration allows for efficient energy transfer processes. This behavior opens avenues for studying complex molecular interactions and dynamic systems in various environments.

CruzFluor sm™ 6 amine exhibits remarkable fluorescence characteristics, emitting light in the 620-750 nm spectrum. Its amine group enables versatile hydrogen bonding and nucleophilic interactions, promoting unique reactivity profiles. The compound's planar structure contributes to enhanced light absorption and stability, while its electronic properties facilitate rapid electron transfer. This behavior allows for intricate studies of molecular dynamics and interactions in diverse chemical contexts.

CruzFluor sm™ 6 maleimide is distinguished by its exceptional photophysical properties, emitting fluorescence in the 620-750 nm range. The maleimide moiety facilitates selective conjugation with thiols, enabling precise targeting in complex systems. Its rigid structure enhances photostability and minimizes non-radiative decay, while the unique electronic configuration supports efficient energy transfer processes. This compound's reactivity and stability make it a valuable tool for probing molecular interactions in various environments.

CruzFluor sm™ 6 succinimidyl ester exhibits remarkable fluorescence in the 620-750 nm range, characterized by its ability to form stable amide bonds through reaction with primary amines. This compound's unique ester functionality promotes rapid conjugation kinetics, allowing for efficient labeling in diverse biochemical contexts. Its robust structure contributes to enhanced photostability, while the electronic properties facilitate effective energy transfer, making it suitable for intricate molecular studies.

CruzFluor™ 700 succinimidyl ester is distinguished by its exceptional fluorescence within the 620-750 nm spectrum, driven by its reactive succinimidyl group that selectively targets primary amines. This compound showcases rapid reaction kinetics, enabling swift conjugation processes. Its unique electronic configuration enhances light absorption and emission efficiency, while its stable backbone ensures resilience against photodegradation, making it ideal for advanced analytical applications.

Chromeo™ 494 alkyne exhibits remarkable photophysical properties within the 620-750 nm range, characterized by its unique alkyne functional group that facilitates distinct molecular interactions. This compound demonstrates efficient energy transfer mechanisms, enhancing its luminescent behavior. Its structural rigidity contributes to a high degree of stability, while the alkyne's reactivity allows for versatile coupling reactions, making it a compelling choice for innovative applications in materials science.

Chromeo™ 642 alkyne showcases exceptional optical characteristics in the 620-750 nm spectrum, driven by its unique alkyne framework that promotes selective molecular interactions. This compound exhibits enhanced photostability and a pronounced ability to undergo rapid electron transfer processes, which can influence reaction kinetics. Its distinctive structural features enable effective conjugation, leading to tailored photonic properties that are advantageous in advanced material development.