Items 191 to 200 of 452 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Pyrogallol | 87-66-1 | sc-203368 sc-203368B sc-203368C sc-203368D | 10 g 50 g 250 g 1 kg | $27.00 $86.00 $265.00 $384.00 | ||
Pyrogallol is a versatile compound in laboratory environments, known for its strong reducing properties and ability to form stable complexes with metal ions. It participates in redox reactions, often acting as an electron donor, which can significantly alter reaction kinetics. Its phenolic structure allows for hydrogen bonding and interactions with various substrates, enhancing its role in analytical chemistry. Additionally, pyrogallol's capacity to absorb oxygen makes it useful in studying oxidative processes. | ||||||
Pyromellitic acid | 89-05-4 | sc-212608 sc-212608A | 100 g 500 g | $40.00 $150.00 | ||
Pyromellitic acid is a polycarboxylic acid characterized by its ability to form strong hydrogen bonds and engage in complexation with metal ions. Its unique structure allows for the formation of stable anhydrides, which can participate in acylation reactions. The compound exhibits significant reactivity due to its multiple carboxyl groups, enabling it to act as a cross-linking agent in polymer chemistry. Additionally, its high degree of symmetry contributes to its distinct physical properties, influencing solubility and crystallization behavior. | ||||||
Trifluoromethanesulfonic acid | 1493-13-6 | sc-203415 sc-203415A sc-203415B | 10 g 50 g 100 g | $33.00 $97.00 $163.00 | ||
Trifluoromethanesulfonic acid is a highly reactive superacid known for its exceptional ability to protonate a wide range of substrates, significantly enhancing reaction rates. Its trifluoromethyl group imparts unique electronic properties, making it a strong electrophile in Friedel-Crafts reactions and other electrophilic aromatic substitutions. The compound's strong acidity and polar nature facilitate its solubility in both polar and nonpolar solvents, enabling diverse applications in organic synthesis and catalysis. | ||||||
Trimethylammonium acetate solution | 6850-27-7 | sc-296627 | 100 ml | $87.00 | 2 | |
Trimethylammonium acetate solution serves as a versatile reagent in laboratory settings, exhibiting unique solvation properties that enhance molecular interactions. Its ability to stabilize charged species facilitates specific ion pairing, which can influence reaction pathways and kinetics. The solution's distinctive viscosity and density characteristics allow for precise manipulation in various experimental conditions, promoting effective diffusion and interaction rates among reactants, thereby ensuring consistent results in complex biochemical systems. | ||||||
Sodium sulfite | 7757-83-7 | sc-203406 sc-203406A | 250 g 2.5 kg | $30.00 $100.00 | ||
Sodium sulfite is a versatile compound known for its reducing properties, particularly in redox reactions. It readily donates electrons, facilitating the conversion of various oxidizing agents. The compound's ability to form sulfite ions in solution enhances its role in preserving the integrity of sensitive reagents. Additionally, its interaction with oxygen leads to the formation of sulfate, influencing reaction kinetics and pathways. Its crystalline form contributes to its solubility, impacting its reactivity in diverse laboratory applications. | ||||||
Potassium phosphate tribasic | 7778-53-2 | sc-250766 sc-250766A | 25 g 500 g | $26.00 $60.00 | ||
Potassium phosphate tribasic is a versatile compound known for its role in stabilizing pH levels through effective buffering. Its unique ability to form hydrogen bonds enhances solubility and promotes interactions with other ions, facilitating complex formation. The compound's tri-basic nature allows it to engage in diverse protonation equilibria, influencing reaction pathways and kinetics. Its crystalline form contributes to its physical stability, making it a reliable choice in various laboratory settings. | ||||||
Iodic acid | 7782-68-5 | sc-211648 sc-211648A | 50 g 250 g | $85.00 $351.00 | ||
Iodic acid is distinguished by its strong oxidizing properties, which facilitate unique redox reactions in various chemical environments. Its molecular structure allows for the formation of iodate ions, influencing the kinetics of reactions involving halogens. The acid exhibits notable acidity, promoting proton transfer mechanisms that enhance its reactivity. Additionally, its interactions with metal ions can lead to the formation of stable complexes, impacting the dynamics of coordination chemistry. | ||||||
Aluminum sulfate octadecahydrate | 7784-31-8 | sc-202928 sc-202928A sc-202928B | 100 g 500 g 2.5 kg | $47.00 $180.00 $660.00 | ||
Aluminum sulfate octadecahydrate exhibits a complex hydration structure that significantly influences its solubility and reactivity. The extensive hydrogen bonding within its lattice enhances its stability in solution, promoting effective ion exchange processes. This compound demonstrates unique coordination chemistry, allowing it to interact with various anions and cations, which can alter its reactivity. Its high water content also plays a crucial role in modulating reaction kinetics, making it a key player in various laboratory applications. | ||||||
Sodium perchlorate monohydrate | 7791-07-3 | sc-203397 sc-203397A | 100 g 500 g | $50.00 $195.00 | ||
Sodium perchlorate monohydrate is a highly soluble salt that exhibits strong oxidizing properties, making it a key player in various chemical reactions. Its unique ability to stabilize perchlorate ions allows for controlled release in redox processes. The compound's hygroscopic nature influences its interaction with moisture, affecting reaction kinetics and stability. Additionally, it can serve as a reagent in the synthesis of other perchlorate derivatives, showcasing its versatility in laboratory applications. | ||||||
Horseradish peroxidase (HRP), RZ 3.0 | 9003-99-0 | sc-391122 sc-391122A sc-391122B | 100 mg 250 mg 5 g | $126.00 $250.00 $4080.00 | 2 | |
Horseradish peroxidase (HRP), RZ 3.0, is a highly efficient enzyme characterized by its ability to catalyze the oxidation of various substrates using hydrogen peroxide. Its unique heme group facilitates electron transfer, enabling rapid reaction kinetics. HRP exhibits distinct substrate specificity, allowing for selective interactions in biochemical assays. The enzyme's stability under varying pH conditions enhances its utility in diverse experimental protocols, making it a reliable choice for oxidative reactions. |