pH Indicators
Items 51 to 54 of 54 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Alizarin yellow GG | 584-42-9 | sc-214521 | 25 g | $112.00 | ||
Alizarin yellow GG is a synthetic dye that exhibits remarkable pH sensitivity due to its unique azo structure, which facilitates protonation and deprotonation processes. This compound undergoes distinct colorimetric changes as pH varies, driven by the resonance stabilization of its conjugated system. Its solubility in aqueous and organic solvents, along with its capacity to form hydrogen bonds, contributes to its dynamic behavior in diverse chemical environments, making it a versatile indicator. | ||||||
7-Hydroxy-4-methyl-3-coumarinylacetic acid | 5852-10-8 | sc-210625 | 100 mg | $109.00 | ||
7-Hydroxy-4-methyl-3-coumarinylacetic acid is characterized by its ability to engage in specific hydrogen bonding interactions, influencing its acidity and solubility. The presence of the hydroxyl and carboxylic acid groups allows for effective proton transfer, leading to distinct pH-dependent behavior. Its unique coumarin structure enhances fluorescence properties, which can be modulated by changes in pH, making it an intriguing compound for studying molecular interactions in varying environments. | ||||||
Patent blue V sodium salt | 20262-76-4 | sc-250653 sc-250653A | 10 g 25 g | $41.00 $66.00 | ||
Patent blue V sodium salt exhibits unique chromatic properties due to its sulfonate groups, which enhance solubility in aqueous environments. Its structure allows for strong ionic interactions, influencing its behavior in different pH conditions. The compound's distinct absorption spectrum shifts with pH changes, providing insights into molecular dynamics. Additionally, its stability in various ionic strengths makes it a subject of interest for studying reaction kinetics and environmental interactions. | ||||||
Propyl red | 2641-01-2 | sc-236489 | 5 g | $116.00 | ||
Propyl red is a pH indicator characterized by its vivid color transition, which occurs in response to changes in acidity. Its molecular structure features a conjugated system that allows for effective electron delocalization, resulting in distinct colorimetric shifts. The compound's sensitivity to protonation and deprotonation processes enables it to serve as a reliable marker for pH variations. Furthermore, its hydrophobic regions contribute to unique solubility behaviors in different solvents, influencing its reactivity and interaction with other chemical species. | ||||||