Items 81 to 90 of 97 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Alphazurine A | 3486-30-4 | sc-214526 sc-214526A sc-214526B | 25 g 100 g 250 g | $38.00 $130.00 $204.00 | 2 | |
Alphazurine A, functioning as a sodium salt, exhibits remarkable chromogenic properties due to its unique conjugated system, which allows for distinct light absorption and emission characteristics. Its interactions with metal ions can lead to complex formation, influencing its stability and reactivity. The compound's solubility in polar solvents enhances its diffusion rates, while its ionic character facilitates charge transfer processes, impacting reaction mechanisms in various chemical environments. | ||||||
Resazurin sodium salt | 62758-13-8 | sc-206037 sc-206037B sc-206037C sc-206037A | 1 g 25 g 100 g 5 g | $56.00 $322.00 $938.00 $102.00 | 17 | |
Resazurin sodium salt is a redox-active compound characterized by its ability to undergo reversible reduction, transitioning between blue and pink forms. This dynamic behavior is attributed to its electron-deficient structure, which engages in specific electron transfer reactions. Its high solubility in aqueous solutions promotes rapid diffusion, while its interactions with biological systems can alter electron flow, influencing metabolic pathways and cellular respiration dynamics. | ||||||
Orange GGN | 2347-72-0 | sc-396944 | 5 mg | $189.00 | ||
Orange GGN is a vibrant dye known for its unique chromophoric structure, which allows it to exhibit distinct colorimetric changes in response to pH variations. This compound interacts with light through specific electronic transitions, leading to pronounced absorbance shifts. Its stability in various solvents enhances its utility in analytical applications, while its reactivity with nucleophiles showcases its potential in diverse chemical pathways, influencing reaction kinetics and product formation. | ||||||
6′-Sialyllactose sodium salt | 157574-76-0 | sc-257003A sc-257003 sc-257003B sc-257003C sc-257003D | 25 mg 50 mg 100 mg 250 mg 500 mg | $135.00 $210.00 $270.00 $460.00 $765.00 | ||
6'-Sialyllactose sodium salt is a complex carbohydrate that exhibits unique binding properties due to its sialic acid moiety, which enhances its interaction with glycan-binding proteins. This compound participates in specific molecular recognition events, influencing cellular signaling pathways. Its solubility in aqueous environments facilitates rapid diffusion, while its structural conformation allows for versatile interactions with other biomolecules, impacting reaction dynamics and stability in biochemical contexts. | ||||||
Protamine sulfate salt from salmon | 53597-25-4 | sc-258046 sc-258046A | 25 g 100 g | $209.00 $632.00 | ||
Protamine sulfate salt, derived from salmon, is a cationic protein that exhibits strong electrostatic interactions with negatively charged molecules, particularly nucleic acids. Its unique structure allows for the formation of stable complexes, influencing molecular aggregation and stability. The protein's high solubility in aqueous solutions enhances its kinetic behavior, promoting rapid interactions in biological systems. Additionally, its ability to modulate charge interactions plays a crucial role in various biochemical pathways. | ||||||
AGN 193109 Sodium Salt | 171746-21-7 | sc-210768 sc-210768A | 1 mg 10 mg | $355.00 $2458.00 | 33 | |
AGN 193109 Sodium Salt is a sodium derivative characterized by its unique ability to engage in specific ionic interactions, enhancing solubility and reactivity in various environments. Its structure facilitates selective binding to target molecules, influencing reaction kinetics and pathways. The compound's distinct electrochemical properties allow for modulation of local pH, which can affect the stability and behavior of surrounding compounds, making it a versatile agent in diverse chemical contexts. | ||||||
2,3-Diphospho-D-glyceric acid pentasodium salt | 102783-53-9 | sc-213964 sc-213964A sc-213964B | 25 mg 100 mg 500 mg | $138.00 $367.00 $1234.00 | 2 | |
2,3-Diphospho-D-glyceric acid pentasodium salt exhibits remarkable chelating properties, enabling it to form stable complexes with metal ions. This interaction enhances its solubility in aqueous solutions and promotes unique reaction pathways. The compound's anionic nature contributes to its ability to modulate ionic strength, influencing the behavior of other solutes. Additionally, its distinct phosphate groups facilitate hydrogen bonding, impacting molecular interactions and stability in various chemical systems. | ||||||
Fura-2, pentasodium salt | 96314-98-6 | sc-391163 | 1 mg | $92.00 | ||
Fura-2, pentasodium salt is a fluorescent calcium indicator that exhibits unique photophysical properties, allowing it to undergo significant spectral shifts upon calcium binding. This property enables it to effectively report on intracellular calcium dynamics. The compound's structure facilitates rapid binding kinetics, making it sensitive to transient changes in calcium concentration. Its solubility in aqueous environments enhances its utility in various biochemical assays, while its anionic character influences interactions with cationic species, affecting overall system behavior. | ||||||
Sodium tetra(p-tolyl)borate | 15738-23-5 | sc-396636 | 500 mg | $160.00 | ||
Sodium tetra(p-tolyl)borate is a versatile reagent known for its unique ability to stabilize reactive intermediates through π-π stacking interactions. This compound exhibits distinct solubility characteristics, allowing it to participate in diverse organic reactions. Its anionic nature enhances nucleophilicity, facilitating rapid reaction kinetics in various coupling processes. Additionally, the steric bulk of the p-tolyl groups influences selectivity in electrophilic substitutions, making it a valuable tool in synthetic chemistry. | ||||||
Anthracene-9,10-dipropionic acid disodium salt | 82767-90-6 | sc-396571 | 10 mg | $235.00 | 4 | |
Anthracene-9,10-dipropionic acid disodium salt is characterized by its strong electron-donating properties, which enhance its reactivity in photochemical processes. The compound exhibits notable solubility in polar solvents, promoting efficient energy transfer in excited states. Its unique structure allows for effective intermolecular interactions, leading to distinct aggregation behaviors. The disodium salt form increases ionic strength, influencing reaction dynamics and enhancing stability in various environments. |