Items 331 to 340 of 452 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Formic acid solution | 64-18-6 | sc-294988 | 100 ml | $254.00 | ||
Formic acid solution is a potent acid that exhibits strong proton-donating capabilities, influencing reaction kinetics in various chemical processes. Its ability to form hydrogen bonds enhances solubility and reactivity with polar compounds. As a reducing agent, it participates in redox reactions, facilitating electron transfer. The solution's low viscosity and high density contribute to its effective mixing and interaction with other reagents, making it a valuable tool in analytical chemistry. | ||||||
Potassium perchlorate (reagent grade) | 7778-74-7 | sc-203359 sc-203359A sc-203359B | 100 g 500 g 1 kg | $53.00 $150.00 $280.00 | ||
Potassium perchlorate is notable for its strong oxidizing properties, which facilitate a range of redox reactions. Its high solubility in water allows for effective ion dissociation, promoting ionic interactions in solution. The compound can participate in exothermic reactions, particularly when combined with reducing agents, leading to rapid energy release. Its stability under various conditions makes it a reliable reagent for studying reaction mechanisms and kinetics in laboratory settings. | ||||||
Potassium periodate | 7790-21-8 | sc-203360 sc-203360A | 100 g 500 g | $148.00 $358.00 | ||
Potassium periodate is distinguished by its ability to act as a powerful oxidizing agent, particularly in organic synthesis. It readily engages in oxidation reactions, converting alcohols to carbonyl compounds through selective pathways. The compound's unique structure allows for the formation of stable intermediates, enhancing reaction specificity. Its solubility in polar solvents facilitates effective ion interactions, making it a versatile reagent for exploring complex reaction dynamics in laboratory experiments. | ||||||
Iodine monochloride | 7790-99-0 | sc-211649 sc-211649A | 25 g 100 g | $66.00 $154.00 | ||
Iodine monochloride is characterized by its ability to engage in halogen exchange reactions, showcasing its role as a versatile reagent in synthetic chemistry. Its polar covalent bond facilitates dipole interactions, enhancing its reactivity with nucleophiles. The compound can act as a Lewis acid, promoting electrophilic addition reactions. Furthermore, its unique molecular geometry influences the stability of intermediates, affecting reaction pathways and kinetics in halogenation processes. | ||||||
Antimony (III) Chloride | 10025-91-9 | sc-202955 sc-202955A sc-202955B | 5 g 100 g 250 g | $50.00 $100.00 $160.00 | ||
Antimony (III) Chloride is a notable Lewis acid, exhibiting strong electrophilic characteristics that facilitate complexation with various nucleophiles. Its ability to form adducts with solvents and ligands enhances its role in catalyzing reactions, particularly in Friedel-Crafts acylation and alkylation processes. The compound's unique dimeric structure in the solid state transitions to a monomeric form in solution, influencing its reactivity and interaction dynamics in synthetic pathways. | ||||||
Calcium phosphate tribasic | 12167-74-7 | sc-211613 | 25 g | $158.00 | ||
Calcium phosphate tribasic is a notable compound characterized by its ability to form stable crystalline structures, which influence its solubility and reactivity in aqueous environments. Its unique ionic interactions contribute to the formation of complex networks, affecting the kinetics of precipitation reactions. The compound's amphoteric nature allows it to react with both acids and bases, facilitating diverse pathways in mineralization processes. Additionally, its role in ion exchange can impact the behavior of surrounding ions in solution. | ||||||
Cyanogum 41 | 39288-95-4 | sc-294113 | 100 g | $60.00 | ||
Cyanogum 41 is a specialized reagent known for its unique reactivity as an acid halide, facilitating selective acylation reactions. Its ability to form stable intermediates with nucleophiles enhances reaction kinetics, allowing for rapid synthesis of complex organic compounds. The compound exhibits distinct solubility characteristics, promoting effective phase separation in various solvents. Additionally, its molecular structure supports diverse functionalization pathways, making it a valuable tool in synthetic chemistry. | ||||||
DIPSO | 68399-80-4 | sc-239813 | 25 g | $78.00 | ||
DIPSO is an intriguing acid halide characterized by its propensity for nucleophilic acyl substitution reactions, which are facilitated by its electrophilic carbonyl group. This compound exhibits a unique ability to form stable adducts with nucleophiles, leading to diverse synthetic pathways. Its distinct steric and electronic properties enhance reactivity, allowing for selective functionalization. Additionally, DIPSO's solubility in various organic solvents contributes to its versatility in laboratory applications. | ||||||
TRAIL Storage and Dilution Buffer | sc-286035 | 500 µl | $112.00 | |||
TRAIL Storage and Dilution Buffer is a specialized formulation designed to maintain optimal conditions for sensitive biochemical assays. Its unique composition allows for effective ionic strength modulation, which is crucial for stabilizing protein interactions. The buffer exhibits a high degree of solubility in aqueous environments, promoting uniform distribution of solutes. Additionally, its low viscosity enhances pipetting accuracy, ensuring precise handling in laboratory settings. | ||||||
Ammonium chloride-ammonium hydroxide buffer solution | sc-291894 sc-291894A | 500 ml 2 L | $80.00 $240.00 | |||
Ammonium chloride-ammonium hydroxide buffer solution is characterized by its ability to maintain a stable pH through the interplay of its constituent ions. The solution exhibits strong ionic interactions, which enhance solubility and promote effective charge distribution. This buffer's unique equilibrium dynamics allow for efficient proton transfer, making it ideal for reactions sensitive to pH fluctuations. Its moderate viscosity aids in the uniform distribution of solutes, optimizing reaction conditions in various laboratory applications. | ||||||