Items 161 to 170 of 390 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Potassium tetraphenylborate | 3244-41-5 | sc-236456 | 1 g | $25.00 | ||
Potassium tetraphenylborate is an intriguing inorganic compound characterized by its unique anionic structure, which features a boron atom surrounded by four phenyl groups. This arrangement imparts significant steric hindrance, influencing its solubility and reactivity. The compound exhibits strong ion-pairing interactions, facilitating the formation of stable complexes with cations. Its ability to act as a non-coordinating anion enhances its role in various electrochemical applications, showcasing distinct pathways in ionic conductivity. | ||||||
Zinc sulfide | 1314-98-3 | sc-251452 | 25 g | $51.00 | ||
Zinc sulfide is an inorganic compound characterized by its luminescent properties, particularly in the form of phosphorescence. This material exhibits a wide band gap, making it an effective semiconductor with potential for optoelectronic applications. Its crystal structure allows for unique exciton dynamics, facilitating energy transfer processes. Additionally, zinc sulfide can participate in various surface reactions, enhancing its reactivity and interaction with other materials in composite systems. | ||||||
Copper(I) oxide | 1317-39-1 | sc-239580 sc-239580A | 25 g 500 g | $43.00 $62.00 | ||
Copper(I) oxide is an inorganic compound notable for its unique electronic properties and its role as a p-type semiconductor. It exhibits a distinctive cubic crystal structure that influences its optical characteristics, including a strong absorption in the visible spectrum. The compound engages in redox reactions, showcasing its ability to participate in electron transfer processes. Its surface chemistry allows for effective adsorption of various species, enhancing its catalytic potential in diverse chemical environments. | ||||||
Silver trifluoroacetate | 2966-50-9 | sc-236881 | 5 g | $48.00 | ||
Silver trifluoroacetate is a notable inorganic compound distinguished by its unique coordination chemistry and reactivity patterns. The silver cation exhibits a propensity for forming strong bonds with the trifluoroacetate anion, leading to the formation of stable complexes. This compound participates in nucleophilic acyl substitution reactions, where the electron-withdrawing trifluoroacetate enhances electrophilicity, promoting efficient reaction kinetics. Its distinct solubility properties further influence its behavior in various chemical environments. | ||||||
Nickel(II) acetylacetonate | 3264-82-2 | sc-250559 sc-250559A | 5 g 25 g | $32.00 $110.00 | ||
Nickel(II) acetylacetonate is a notable inorganic complex distinguished by its bidentate ligand coordination, where acetylacetonate ligands effectively chelate the nickel ion. This chelation enhances the stability of the complex and influences its electronic properties, leading to unique redox behavior. The compound exhibits distinct thermal and magnetic characteristics, making it a subject of interest in studies of coordination chemistry and material science, particularly in the context of catalysis and thin-film deposition. | ||||||
Ferric citrate | 334024-15-6 | sc-235134 | 250 g | $58.00 | ||
Ferric citrate is a distinctive inorganic compound that showcases its ability to chelate with various anions and ligands, forming stable complexes. This chelation enhances its solubility in aqueous environments and influences its reactivity in redox processes. The compound participates in electron transfer reactions, demonstrating unique kinetic behavior. Its crystalline structure contributes to its physical properties, allowing for diverse interactions in complexation and precipitation reactions. | ||||||
Tris(trimethylsilyl) borate | 4325-85-3 | sc-237395 | 25 g | $67.00 | ||
Tris(trimethylsilyl) borate is an intriguing inorganic compound known for its unique ability to stabilize reactive intermediates through coordination with Lewis bases. Its trimethylsilyl groups enhance its lipophilicity, facilitating interactions with organic solvents. This compound exhibits distinctive reactivity patterns, particularly in nucleophilic substitution reactions, where it acts as a boron source. Its molecular structure allows for effective steric hindrance, influencing reaction kinetics and selectivity in synthetic pathways. | ||||||
Pyrophosphoric acid | 2466-09-3 | sc-250819 sc-250819A | 100 g 500 g | $87.00 $337.00 | 1 | |
Pyrophosphoric acid is a unique inorganic acid known for its ability to form polyphosphate chains through condensation reactions. This property allows it to participate in complexation with metal ions, enhancing its role in catalysis and material synthesis. Its strong acidity promotes rapid proton transfer, influencing reaction kinetics in various chemical processes. Additionally, it exhibits hygroscopic behavior, readily absorbing moisture from the environment, which can affect its stability and reactivity. | ||||||
Trioctylphosphine | 4731-53-7 | sc-296638 sc-296638A | 25 ml 500 ml | $42.00 $480.00 | ||
Trioctylphosphine is a notable inorganic compound characterized by its long hydrocarbon chains, which impart significant lipophilicity and enhance solubility in nonpolar environments. This phosphine exhibits unique coordination chemistry, forming stable complexes with transition metals, thereby influencing catalytic processes. Its sterically bulky structure affects reaction kinetics, promoting selective pathways in organometallic reactions. Additionally, it can participate in ligand exchange processes, showcasing its versatility in various chemical environments. | ||||||
Boron trifluoride-methanol-complex solution | 2802-68-8 | sc-234204 sc-234204A | 500 ml 1 L | $78.00 $108.00 | ||
Boron trifluoride-methanol-complex solution is an intriguing inorganic compound characterized by its Lewis acid behavior, facilitating the formation of adducts through coordination with electron-rich species. This complex exhibits unique solvation dynamics, enhancing its reactivity in nucleophilic substitution reactions. The solution's ability to stabilize transition states contributes to its role in accelerating reaction rates, while its polar nature influences solubility and interaction with various substrates, making it a versatile reagent in synthetic chemistry. |