Items 371 to 380 of 452 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Lithium Metaborate | 13453-69-5 | sc-203112 | 100 g | $94.00 | ||
Lithium Metaborate is a unique compound characterized by its ability to form stable complexes with various metal ions, enhancing its role in analytical chemistry. Its distinct ionic interactions facilitate the formation of borate esters, which can influence reaction pathways and kinetics. The compound exhibits notable thermal stability, allowing it to act as a flux in fusion processes. Additionally, its low viscosity in molten form aids in the efficient transport of reactants during high-temperature applications. | ||||||
Reinecke salt | 13573-16-5 | sc-203369 sc-203369A | 25 g 100 g | $164.00 $492.00 | 2 | |
Reinecke salt is a unique coordination compound that exhibits distinct properties as a standard in laboratory settings. Its ability to form stable complexes with transition metals is attributed to its chelating nature, which enhances selectivity in various reactions. The compound demonstrates notable solubility in polar solvents, facilitating its use in diverse analytical techniques. Furthermore, Reinecke salt's distinct colorimetric changes during reactions provide visual cues for monitoring reaction progress and completion. | ||||||
L-β-Imidazolelactic acid | 14403-45-3 | sc-286037 sc-286037A | 100 mg 1 g | $200.00 $400.00 | ||
L-β-Imidazolelactic acid is a versatile compound known for its unique ability to participate in various biochemical pathways. Its structure facilitates specific hydrogen bonding interactions, enhancing its reactivity in enzymatic processes. The compound exhibits notable stability under varying pH conditions, making it an ideal candidate for studying reaction kinetics. Furthermore, its solubility in polar solvents allows for efficient integration into diverse experimental setups, promoting reliable results in laboratory analyses. | ||||||
HEPPS | 16052-06-5 | sc-286008 sc-286008A | 25 g 100 g | $60.00 $145.00 | ||
HEPPS is a versatile buffering agent characterized by its unique ability to stabilize pH across a wide range of conditions. Its distinct molecular structure facilitates strong ionic interactions, promoting solubility in diverse solvents. The compound's capacity for specific hydrogen bonding enhances its role in stabilizing biomolecules during experimental procedures. Furthermore, HEPPS demonstrates low reactivity with other chemical species, ensuring minimal disruption in complex biochemical environments. | ||||||
Azide, 2% solution | 26628-22-8 | sc-291918 sc-291918A | 5 ml 25 ml | $25.00 $98.00 | ||
Azide, 2% solution is a versatile reagent known for its ability to act as a potent nucleophile, engaging in various substitution reactions. Its unique structure allows for efficient azide-alkyne cycloaddition, a key reaction in click chemistry. The solution exhibits remarkable stability under standard laboratory conditions, while its reactivity can be finely tuned through concentration adjustments. This makes it an essential tool for probing reaction kinetics and exploring molecular interactions in synthetic pathways. | ||||||
TAPS solution, 0.25M | 29915-38-6 (solid) | sc-301862 | 200 ml | $102.00 | ||
TAPS solution, at 0.25M concentration, serves as a versatile buffer system, effectively maintaining pH stability in biochemical assays. Its unique ability to form hydrogen bonds facilitates specific molecular interactions, enhancing solubility for various biomolecules. The solution's ionic strength influences reaction kinetics, promoting efficient enzyme activity and substrate binding. Additionally, TAPS exhibits low reactivity with common lab reagents, ensuring minimal interference in experimental setups. | ||||||
ADA disodium salt | 41689-31-0 | sc-284940 | 100 g | $105.00 | ||
ADA disodium salt is a unique compound characterized by its ability to form stable complexes with metal ions, enhancing its role in various analytical techniques. Its distinct ionic interactions facilitate the formation of micelles, which can improve solubilization of hydrophobic substances. The compound also exhibits notable thermal stability, allowing it to maintain integrity under varying conditions. Furthermore, its dual anionic nature contributes to its effectiveness in modulating reaction kinetics, making it a key player in complex biochemical systems. | ||||||
TABS | 54960-65-5 | sc-296443 sc-296443A | 25 g 100 g | $215.00 $712.00 | ||
TABS is a versatile acid halide known for its reactivity and ability to form stable intermediates in organic synthesis. Its unique structure allows for selective acylation reactions, promoting efficient carbon-carbon bond formation. The compound exhibits distinct electrophilic properties, enabling it to engage in nucleophilic attacks with various substrates. Additionally, TABS demonstrates a propensity for forming cyclic intermediates, which can enhance reaction kinetics and yield in synthetic pathways. | ||||||
BES sodium salt | 66992-27-6 | sc-263026 | 100 g | $166.00 | ||
BES sodium salt is a highly effective buffering agent that stabilizes pH levels in biochemical assays. Its unique ability to interact with various biomolecules allows for precise control over reaction environments. The compound exhibits distinct solubility characteristics, enhancing its compatibility with diverse solvents. Additionally, its ionic nature promotes specific molecular interactions, facilitating enzyme activity and optimizing reaction kinetics in laboratory settings. | ||||||
Ethylenediaminetetraacetic acid diammonium copper salt solution | 67989-88-2 | sc-285567 | 250 ml | $29.00 | ||
Ethylenediaminetetraacetic acid diammonium copper salt solution is characterized by its capacity to chelate metal ions, particularly copper, forming stable complexes that influence redox reactions. This solution exhibits unique coordination properties, allowing for selective binding and modulation of metal ion availability. Its aqueous solubility enhances its reactivity in various chemical pathways, while its pH sensitivity can alter complex stability, impacting reaction kinetics and interactions with other ligands. |