Items 1 to 10 of 470 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Hydrogen Peroxide | 7722-84-1 | sc-203336 sc-203336A sc-203336B | 100 ml 500 ml 3.8 L | $30.00 $60.00 $93.00 | 27 | |
Hydrogen peroxide serves as a powerful synthetic reagent, notable for its role as an oxidizing agent in various organic transformations. Its unique ability to generate free radicals facilitates selective oxidation, enabling the cleavage of C-C bonds and the functionalization of hydrocarbons. Additionally, its dual nature as both a nucleophile and electrophile allows it to participate in diverse reaction pathways, enhancing its utility in synthetic chemistry. Its high reactivity and ability to form peracids further expand its application in complex reaction schemes. | ||||||
(2-Hydroxypropyl)-β-cyclodextrin solution | sc-288158 | 10 ml | $217.00 | 1 | ||
(2-Hydroxypropyl)-β-cyclodextrin solution acts as a versatile synthetic reagent, characterized by its ability to form inclusion complexes with a variety of guest molecules. This property enhances solubility and stability, facilitating controlled release and selective interactions. Its unique hydrophilic and hydrophobic regions promote specific molecular recognition, influencing reaction kinetics and pathways. Additionally, it can modulate the reactivity of encapsulated compounds, making it a valuable tool in synthetic methodologies. | ||||||
DPPH, Free Radical | 1898-66-4 | sc-202591 sc-202591A | 50 mg 1 g | $46.00 $210.00 | 15 | |
DPPH, a stable free radical, serves as a synthetic reagent known for its distinctive electron transfer properties. It exhibits a deep violet color, which diminishes upon interaction with antioxidants, allowing for quantitative analysis of radical scavenging activity. The unique resonance stabilization of its unpaired electron contributes to its reactivity, influencing reaction kinetics. DPPH's ability to engage in selective redox reactions makes it a crucial component in studying oxidative stress and radical mechanisms. | ||||||
Acrylic acid N-hydroxysuccinimide ester | 38862-24-7 | sc-233817 | 1 g | $107.00 | 2 | |
Acrylic acid N-hydroxysuccinimide ester is a versatile synthetic reagent characterized by its ability to form stable covalent bonds with nucleophiles. Its unique structure facilitates efficient Michael addition reactions, enabling selective modifications in complex organic syntheses. The presence of the N-hydroxysuccinimide moiety enhances its reactivity, promoting rapid esterification and acylation processes. This compound's distinct reactivity profile makes it a valuable tool in various synthetic pathways. | ||||||
Potassium Phosphate, Monobasic | 7778-77-0 | sc-203211 sc-203211A sc-203211B sc-203211C | 500 g 2 kg 5 kg 10 kg | $20.00 $50.00 $105.00 $475.00 | 3 | |
Potassium Phosphate, Monobasic serves as a crucial synthetic reagent, notable for its role in buffering systems and pH regulation. Its ability to interact with metal ions enhances solubility and stability in various reactions. This compound exhibits unique ionic interactions, facilitating the formation of complexes that can influence reaction kinetics. Additionally, its hygroscopic nature allows it to maintain moisture levels, impacting the reactivity of other compounds in synthetic processes. | ||||||
Sodium Phosphate, Dibasic | 7558-79-4 | sc-203277 sc-203277A sc-203277D sc-203277B sc-203277C | 500 g 1 kg 2 kg 5 kg 10 kg | $56.00 $173.00 $234.00 $373.00 $576.00 | 11 | |
Sodium Phosphate, Dibasic is a versatile synthetic reagent characterized by its ability to act as a buffering agent, stabilizing pH levels in various chemical environments. Its unique ionic structure promotes effective interactions with cations, enhancing solubility and facilitating complex formation. This compound also exhibits distinct hydration properties, which can influence reaction dynamics and kinetics, making it a valuable component in various synthetic pathways. | ||||||
4-Sulfocalix[4]arene sodium salt | 151657-13-5 | sc-238956 | 500 mg | $276.00 | ||
4-Sulfocalix[4]arene sodium salt is a unique synthetic reagent known for its ability to form host-guest complexes through non-covalent interactions, such as hydrogen bonding and π-π stacking. Its distinctive cavity structure allows for selective encapsulation of small molecules, enhancing reaction specificity. Additionally, its anionic nature contributes to increased solubility in polar solvents, facilitating diverse reaction pathways and improving overall reaction efficiency. | ||||||
1,3-Di-Boc-2-(2-hydroxyethyl)guanidine | 215050-11-6 | sc-251579 | 1 g | $97.00 | ||
1,3-Di-Boc-2-(2-hydroxyethyl)guanidine is a versatile synthetic reagent characterized by its ability to participate in nucleophilic substitution reactions due to the presence of guanidine functionality. Its Boc (tert-butyloxycarbonyl) protecting groups enhance stability and solubility, allowing for controlled deprotection under mild conditions. The compound exhibits unique reactivity patterns, enabling the formation of diverse derivatives through selective functionalization, making it a valuable tool in synthetic chemistry. | ||||||
2-Picoline borane complex | 3999-38-0 | sc-288295 sc-288295A | 5 g 50 g | $62.00 $516.00 | 1 | |
2-Picoline borane complex serves as a potent synthetic reagent, notable for its ability to facilitate reduction reactions through its borane component. The complex exhibits unique coordination chemistry, allowing for selective interactions with various electrophiles. Its sterically hindered structure enhances reaction kinetics, promoting efficient transformations. Additionally, the presence of the picoline moiety contributes to its solubility and reactivity, making it a distinctive choice for complex synthetic pathways. | ||||||
Sodium carbonate, anhydrous | 497-19-8 | sc-203382 sc-203382A sc-203382B | 500 g 1 kg 2.5 kg | $25.00 $79.00 $122.00 | ||
Sodium carbonate, anhydrous, is a versatile synthetic reagent known for its role in facilitating various chemical reactions, particularly in the realm of acid-base chemistry. Its ability to act as a mild base allows it to effectively neutralize acids, promoting the formation of carbonates and bicarbonates. The compound's hygroscopic nature enhances its reactivity by influencing solvent interactions, while its crystalline structure contributes to its stability and ease of handling in diverse synthetic applications. |