Ex 380-450 nm Violet

Chromeo™ P429 is an innovative acid halide distinguished by its unique reactivity profile and selective electrophilic behavior. It exhibits pronounced interactions with nucleophiles, facilitating rapid acylation reactions. The compound's structural features promote distinct steric effects, influencing reaction pathways and kinetics. Additionally, its ability to form stable intermediates enhances its utility in synthetic applications, showcasing a remarkable balance between reactivity and stability.

mFluor™ Violet 450-dUTP is a specialized nucleotide analog characterized by its exceptional fluorescence properties, particularly under excitation wavelengths of 380-450 nm. This compound exhibits strong binding affinity to complementary nucleic acid sequences, enhancing signal intensity in detection assays. Its unique structural modifications allow for efficient incorporation into DNA during synthesis, promoting distinct hybridization dynamics and enabling precise monitoring of molecular interactions in various biochemical contexts.

FMOC-Glu(DABCYL)-OH is a fluorescently labeled amino acid derivative that exhibits unique photophysical properties when excited within the 380-450 nm range. This compound features a distinct DABCYL moiety, which serves as a quencher, allowing for effective energy transfer in FRET applications. Its ability to form stable interactions with peptide chains enhances its utility in studying protein conformations and dynamics, while its solubility characteristics facilitate diverse experimental setups.

7-Acetoxy-1-methylquinolinium iodide is a unique compound that exhibits intriguing photochemical behavior when excited in the 380-450 nm range. Its structure allows for efficient electron transfer processes, leading to distinct fluorescence characteristics. The presence of the acetoxy group enhances its reactivity, facilitating specific interactions with nucleophiles. Additionally, its ionic nature contributes to solubility in polar solvents, making it suitable for various experimental conditions.

Carbostyril 124 is a distinctive compound known for its remarkable photophysical properties within the 380-450 nm range. Its unique molecular architecture promotes strong π-π stacking interactions, enhancing its stability and fluorescence efficiency. The compound's ability to undergo rapid intramolecular charge transfer contributes to its dynamic reactivity, while its hydrophobic characteristics influence solubility in non-polar environments, making it an intriguing subject for studies in photochemistry and material science.

2-Methoxy-2,4-diphenyl-3(2H)-furanone exhibits intriguing photochemical behavior in the 380-450 nm range, characterized by its ability to form hydrogen bonds that stabilize excited states. This compound demonstrates unique electron-donating properties, facilitating efficient energy transfer processes. Its planar structure allows for effective conjugation, leading to enhanced light absorption and reactivity, making it a compelling candidate for exploring photophysical phenomena and reaction mechanisms.

8-Isothiocyanatopyrene-1,3,6-trisulfonic acid trisodium salt showcases remarkable fluorescence properties within the 380-450 nm spectrum, attributed to its highly conjugated structure. The presence of sulfonate groups enhances solubility and ionic interactions, promoting unique aggregation behavior in aqueous environments. This compound exhibits distinct photostability and reactivity, enabling it to participate in various electron transfer processes, making it a subject of interest in studies of molecular dynamics and photonic applications.

Coumarin 337 exhibits exceptional photophysical characteristics, particularly in the 380-450 nm range, due to its rigid, planar structure that facilitates efficient energy transfer. Its strong fluorescence is influenced by intramolecular hydrogen bonding, which stabilizes excited states and enhances quantum yield. The compound's unique solvent-dependent behavior leads to varied emission profiles, making it a fascinating subject for exploring solvent interactions and environmental effects on luminescence.

10-(3-Sulfopropyl)acridinium betaine is a luminescent compound that exhibits remarkable photostability and a high quantum yield in the 380-450 nm range. Its unique zwitterionic structure promotes strong dipole-dipole interactions, enhancing solubility in polar solvents. The compound's emission properties are sensitive to pH changes, allowing for distinct fluorescence shifts. Additionally, its ability to form aggregates can lead to intriguing self-assembly behaviors, influencing its photophysical responses.

4-(2-Aminoethylamino)-7-(N,N-dimethylsulfamoyl)benzofurazan is a fluorescent compound characterized by its strong emission in the 380-450 nm range. Its unique benzofurazan core facilitates efficient electron transfer processes, enhancing its photochemical stability. The presence of amino and sulfamoyl groups contributes to its solubility in various media and allows for specific hydrogen bonding interactions, which can influence its reactivity and aggregation behavior in solution.