Items 1 to 10 of 228 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Deferoxamine mesylate | 138-14-7 | sc-203331 sc-203331A sc-203331B sc-203331C sc-203331D | 1 g 5 g 10 g 50 g 100 g | $255.00 $1039.00 $2866.00 $4306.00 $8170.00 | 19 | |
Deferoxamine mesylate functions as a chelator by forming stable complexes with ferric ions, effectively sequestering iron from biological systems. Its unique hydroxamic acid groups facilitate strong coordination with metal ions, enhancing its selectivity and binding affinity. This interaction alters the redox potential of iron, impacting various biochemical pathways. The compound exhibits rapid kinetics in iron binding, making it effective in modulating metal ion availability in diverse environments. | ||||||
(2-Hydroxypropyl)-β-cyclodextrin solution | sc-288158 | 10 ml | $217.00 | 1 | ||
(2-Hydroxypropyl)-β-cyclodextrin solution acts as a chelator by encapsulating metal ions within its hydrophobic cavity, creating stable inclusion complexes. This unique structure allows for selective binding, enhancing solubility and stability of the metal ions. The compound's ability to form host-guest interactions facilitates the modulation of metal ion reactivity and bioavailability, while its favorable kinetics promote efficient metal ion sequestration in various conditions. | ||||||
EDTA, Disodium Salt, Dihydrate | 6381-92-6 | sc-29092A sc-29092 | 100 g 500 g | $48.00 $98.00 | 16 | |
EDTA, Disodium Salt, Dihydrate functions as a chelator by forming strong, stable complexes with metal ions through multiple coordination sites. Its unique structure allows for the formation of octahedral complexes, enhancing the solubility of otherwise insoluble metal salts. The chelation process is characterized by rapid kinetics, enabling effective metal ion binding in diverse environments. This compound's high affinity for divalent and trivalent metals makes it particularly effective in controlling metal ion concentrations. | ||||||
EGTA/AM | 99590-86-0 | sc-203937 | 10 mg | $267.00 | 4 | |
EGTA/AM acts as a chelator by selectively binding calcium ions with high specificity, utilizing its unique structure that features multiple carboxylate groups. This compound exhibits a remarkable ability to modulate calcium levels, influencing various biochemical pathways. Its chelation kinetics are notably fast, allowing for efficient metal ion sequestration. Additionally, EGTA/AM's lipophilic properties facilitate cellular permeability, enhancing its interaction with target ions in biological systems. | ||||||
EDTA, 0.5 M, pH 8.0 | 60-00-4 | sc-203932 | 100 ml | $19.00 | 7 | |
EDTA, at a concentration of 0.5 M and pH 8.0, functions as a potent chelator by forming stable complexes with a variety of metal ions through its multiple carboxylate and amine groups. This compound exhibits a high affinity for divalent and trivalent metals, effectively reducing their bioavailability. Its chelation process is characterized by rapid kinetics, enabling swift metal ion capture, while its solubility in aqueous solutions enhances its accessibility for various applications. | ||||||
Ethylenediaminetetra(methylenephosphonic acid) | 1429-50-1 | sc-300682 sc-300682A sc-300682B sc-300682C | 5 g 25 g 100 g 500 g | $37.00 $57.00 $128.00 $552.00 | 1 | |
Ethylenediaminetetra(methylenephosphonic acid) acts as a highly effective chelator, engaging metal ions through its unique phosphonic acid groups. This compound forms strong, stable complexes, particularly with transition metals, by utilizing its multiple binding sites. The chelation process is marked by significant selectivity and affinity, allowing for the modulation of metal ion reactivity. Its solubility in water facilitates easy integration into various environments, enhancing its interaction dynamics. | ||||||
Sodium phytate | 14306-25-3 | sc-203329 | 25 g | $120.00 | 2 | |
Sodium Phytate serves as a potent chelator, characterized by its ability to form stable complexes with divalent and trivalent metal ions through its multiple phosphate groups. This compound exhibits a unique capacity for selective binding, which alters the bioavailability of metals in various systems. Its high solubility in aqueous environments promotes effective interaction with metal ions, influencing their reactivity and transport properties. The chelation kinetics are marked by rapid association and dissociation rates, enhancing its functional versatility. | ||||||
FURA 2/AM | 108964-32-5 | sc-203052 sc-203052A sc-203052B | 50 µg 1 mg 50 mg | $32.00 $146.00 $3874.00 | 17 | |
FURA 2/AM is a fluorescent chelator that selectively binds calcium ions, facilitating the study of intracellular calcium dynamics. Its unique esterified structure allows for cell permeability, enabling real-time monitoring of calcium fluctuations within live cells. The compound exhibits distinct fluorescence properties upon calcium binding, providing a sensitive readout of ion concentration changes. This dynamic interaction enhances our understanding of calcium signaling pathways and cellular responses. | ||||||
Nitrilotriacetic acid | 139-13-9 | sc-215578 sc-215578A | 5 g 100 g | $30.00 $71.00 | ||
Nitrilotriacetic acid is a versatile chelator known for its ability to form stable complexes with metal ions through multiple coordination sites. Its tridentate nature allows for strong binding interactions, effectively sequestering metals and preventing precipitation. The compound's unique structure promotes selective metal ion affinity, influencing reaction kinetics and enhancing solubility in various environments. This behavior is crucial in applications requiring precise metal ion control and manipulation. | ||||||
EDTA, Tetrasodium Tetrahydrate Salt | 13235-36-4 | sc-204735A sc-204735 | 100 g 500 g | $25.00 $48.00 | 2 | |
EDTA, Tetrasodium Tetrahydrate Salt, is a powerful chelating agent characterized by its ability to form highly stable, octadentate complexes with a wide range of metal ions. Its unique structure allows for multiple binding interactions, effectively disrupting metal ion solvation shells and enhancing solubility. The compound's strong affinity for divalent and trivalent metals influences reaction pathways, facilitating metal ion removal and improving overall system stability in diverse chemical environments. |