Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Pyrogallol Red | 32638-88-3 | sc-215766 sc-215766A | 1 g 5 g | $207.00 $513.00 | ||
Pyrogallol Red is a versatile chelating agent known for its ability to form stable complexes with metal ions through its hydroxyl and carboxyl functional groups. This interaction leads to distinct colorimetric changes, facilitating sensitive detection of trace metals. The compound's unique electron-donating properties enhance its reactivity, allowing for rapid complexation kinetics. Its solubility in various solvents further aids in diverse analytical applications, making it a valuable tool in metal ion analysis. | ||||||
Nickel ionophore II | 14609-54-2 | sc-228828 sc-228828A sc-228828B | 250 mg 1 g 5 g | $94.00 $249.00 $638.00 | ||
Nickel ionophore II is a selective ligand that exhibits a strong affinity for nickel ions, facilitating their transport across biological membranes. Its unique coordination chemistry allows for the formation of stable complexes, characterized by specific geometric arrangements that enhance metal ion mobility. The compound's ability to modulate ion transport dynamics is influenced by its hydrophobic regions, which interact with lipid bilayers, promoting efficient nickel detection in various environments. | ||||||
Chromeazurol S | 1667-99-8 | sc-252601 sc-252601A sc-252601B sc-252601C | 25 g 100 g 250 g 1 kg | $113.00 $301.00 $566.00 $1826.00 | ||
Chromeazurol S is a versatile chelating agent known for its ability to form stable complexes with various metal ions, particularly iron. Its unique structure allows for selective binding through multiple coordination sites, leading to distinct colorimetric changes that facilitate visual detection. The compound's interaction with metal ions is influenced by its electronic properties, which enhance sensitivity and specificity, making it a valuable tool in analytical chemistry for metal ion quantification. | ||||||
Cupferron | 135-20-6 | sc-214782 | 25 g | $54.00 | ||
Cupferron is a selective reagent that exhibits strong complexation with transition metals, particularly those in oxidation states +2 and +3. Its unique ability to form chelate rings enhances stability and solubility in various solvents. The compound's reaction kinetics are characterized by rapid formation of metal-ligand complexes, which can be monitored through spectrophotometric methods. This behavior allows for sensitive detection and quantification of metals in diverse analytical applications. | ||||||
Dithizone | 60-10-6 | sc-206031A sc-206031 | 10 g 50 g | $90.00 $332.00 | 2 | |
Dithizone is a highly sensitive chelating agent that forms stable complexes with heavy metals, particularly lead, mercury, and cadmium. Its unique thiol functional groups enable strong interactions with metal ions, resulting in distinct colorimetric changes that facilitate visual detection. The compound exhibits rapid kinetics in metal binding, allowing for quick analysis. Additionally, its solubility in organic solvents enhances its versatility in various extraction and analytical techniques. | ||||||
Chromoxane Cyanine R | 3564-18-9 | sc-255022 | 25 g | $41.00 | ||
Chromoxane Cyanine R is a specialized dye known for its ability to selectively bind to metal ions, particularly those of transition metals. Its unique chromophoric structure allows for distinct color shifts upon complexation, providing a visual cue for metal presence. The compound exhibits rapid reaction kinetics, facilitating swift detection processes. Additionally, its solubility in various solvents enhances its applicability in diverse analytical methods, making it a valuable tool in metal detection. | ||||||
Gallium(III) sulfide | 12024-22-5 | sc-358672 | 5 g | $194.00 | ||
Gallium(III) sulfide is a semiconductor compound that exhibits unique optical properties, particularly in its interaction with metal ions. Its bandgap allows for effective photoluminescence, which can be harnessed for sensitive detection of metals. The compound's surface reactivity enables it to form stable complexes with various metal ions, enhancing selectivity. Additionally, its crystalline structure contributes to distinct electronic pathways, facilitating efficient charge transfer during detection processes. |