Redox Indicators
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Methylene blue trihydrate | 7220-79-3 | sc-203744 sc-203744A | 5 g 25 g | $32.00 $62.00 | 3 | |
Methylene blue trihydrate acts as a versatile redox agent, characterized by its ability to undergo reversible oxidation and reduction processes. This compound exhibits distinct electron transfer dynamics, facilitating rapid interconversion between its oxidized and reduced forms. Its unique planar structure enhances π-π stacking interactions, promoting effective electron delocalization. Additionally, the trihydrate form influences solubility and stability, impacting reaction kinetics in various redox environments. | ||||||
α-Naphthoflavone | 604-59-1 | sc-257037 sc-257037A sc-257037B sc-257037C | 1 g 5 g 25 g 100 g | $34.00 $46.00 $156.00 $500.00 | 3 | |
α-Naphthoflavone serves as a notable redox agent, distinguished by its capacity for electron transfer through a series of complex oxidation states. Its unique polycyclic structure allows for significant resonance stabilization, enhancing its reactivity. The compound's ability to form charge-transfer complexes with various substrates facilitates diverse reaction pathways. Furthermore, its hydrophobic characteristics influence solubility and interaction with biological membranes, affecting its kinetic behavior in redox reactions. | ||||||
Resazurin sodium salt | 62758-13-8 | sc-206037 sc-206037B sc-206037C sc-206037A | 1 g 25 g 100 g 5 g | $57.00 $328.00 $957.00 $104.00 | 17 | |
Resazurin sodium salt is a versatile redox indicator characterized by its ability to undergo reversible reduction to resorufin, a more fluorescent compound. This transformation is facilitated by electron transfer processes that are sensitive to environmental conditions. The compound's unique structure allows for strong interactions with various electron donors, influencing reaction kinetics. Its solubility in aqueous solutions enhances its accessibility for redox reactions, making it a valuable tool in assessing oxidative states. | ||||||
Barium diphenylamine-4-sulfonate | 6211-24-1 | sc-239271 | 5 g | $62.00 | ||
Barium diphenylamine-4-sulfonate serves as a notable redox indicator, exhibiting distinct electron transfer properties. Its unique molecular structure enables effective interactions with oxidizing agents, facilitating rapid redox reactions. The compound's stability in diverse environments allows for consistent performance in various conditions. Additionally, its ability to form charge-transfer complexes enhances its sensitivity, making it a reliable choice for monitoring redox processes in analytical applications. | ||||||
Sulfonazo III sodium salt | 164581-28-6 | sc-229348 sc-229348A | 5 g 25 g | $156.00 $555.00 | ||
Sulfonazo III sodium salt is a versatile redox indicator characterized by its unique chelating ability, which allows it to form stable complexes with metal ions. This interaction alters its electronic structure, leading to distinct colorimetric changes during redox reactions. The compound exhibits rapid kinetics, enabling swift detection of oxidation states. Its solubility in aqueous solutions enhances its applicability, while its pH sensitivity further fine-tunes its performance in diverse chemical environments. | ||||||
Diphenylamine | 122-39-4 | sc-205995 sc-205995A | 100 g 1 kg | $113.00 $525.00 | ||
Diphenylamine is a notable redox-active compound that undergoes reversible oxidation and reduction processes, primarily through the formation of radical cations. Its unique electron-donating properties facilitate strong intermolecular interactions, influencing reaction kinetics and stability. The compound's ability to participate in electron transfer reactions is enhanced by its planar structure, which allows for effective π-π stacking. Additionally, diphenylamine's distinct colorimetric response during redox transitions makes it a valuable tool for monitoring oxidative states in various chemical systems. | ||||||
Safranin T | 477-73-6 | sc-203758 sc-203758A | 25 g 100 g | $49.00 $108.00 | 1 | |
Safranin T is a vibrant redox-active dye characterized by its ability to undergo reversible electron transfer reactions, primarily through the formation of stable radical species. Its planar, conjugated structure promotes efficient π-π interactions, enhancing its reactivity and facilitating rapid electron exchange. The dye exhibits distinct spectral shifts during redox processes, allowing for precise monitoring of electron dynamics. Additionally, its strong affinity for various substrates can influence reaction pathways and kinetics, making it a versatile compound in redox chemistry. | ||||||
N,N′-Diphenylbenzidine | 531-91-9 | sc-257885 | 10 g | $97.00 | ||
N,N'-Diphenylbenzidine is a notable redox-active compound distinguished by its ability to form stable cationic and anionic species during electron transfer processes. Its extended conjugated system allows for significant delocalization of charge, which enhances its reactivity. The compound exhibits unique electrochemical behavior, with distinct oxidation and reduction potentials that facilitate selective electron transfer. Its interactions with various solvents can also influence reaction kinetics, making it a subject of interest in redox studies. | ||||||
1,1′-Dibenzyl-4,4′-bipyridinium dichloride | 1102-19-8 | sc-213422 sc-213422A | 250 mg 1 g | $28.00 $53.00 | ||
1,1'-Dibenzyl-4,4'-bipyridinium dichloride is a redox-active compound characterized by its ability to undergo reversible electron transfer, leading to the formation of stable radical cations. The bipyridinium structure promotes strong π-π stacking interactions, enhancing its electrochemical properties. Its distinct redox potentials enable selective reactivity in various environments, while solvent interactions can significantly modulate its reaction kinetics, making it a compelling subject for redox chemistry exploration. | ||||||