Items 21 to 27 of 27 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Calcium carbonate-13C | 287389-46-2 | sc-234262 | 5 g | $815.00 | ||
Calcium carbonate-13C is an intriguing isotopic variant of calcium carbonate, distinguished by its stable carbon isotope composition. This compound participates in unique carbon cycling processes, influencing the kinetics of carbonate precipitation and dissolution in aquatic systems. Its isotopic signature can provide insights into biogeochemical pathways, enhancing our understanding of carbon sequestration and environmental changes. The distinct molecular interactions within its crystalline structure also affect its reactivity in various geological contexts. | ||||||
Acid fuchsin calcium salt | 123334-10-1 | sc-214473 sc-214473A | 25 g 100 g | $71.00 $224.00 | ||
Acid fuchsin calcium salt exhibits unique properties as a calcium compound, characterized by its vibrant coloration and ability to form stable complexes with various metal ions. Its interactions with proteins and other biomolecules can alter reaction kinetics, influencing dye-binding mechanisms. The compound's solubility and pH sensitivity contribute to its behavior in different environments, affecting its stability and reactivity in complex chemical systems. | ||||||
Calcium 2-Hydroxy-4-(methylthio)butyrate | 4857-44-7 | sc-486869 | 25 g | $309.00 | ||
Calcium 2-Hydroxy-4-(methylthio)butyrate showcases distinctive characteristics as a calcium derivative, particularly in its ability to engage in specific chelation with anions and metal ions. This compound can influence enzymatic activity through modulation of calcium-dependent pathways, enhancing or inhibiting biochemical reactions. Its unique structural features allow for selective interactions, impacting solubility and reactivity in diverse chemical environments, thus playing a role in complexation dynamics. | ||||||
Phytin | 3615-82-5 | sc-487976 sc-487976A | 25 g 500 g | $41.00 $286.00 | ||
Phytin, a complex polyphosphate, plays a crucial role in mineral interactions, particularly with calcium ions. Its unique ability to form stable complexes facilitates the regulation of calcium homeostasis in biological systems. The compound's multi-functional phosphate groups enable it to participate in energy transfer and storage processes. Additionally, Phytin's structural flexibility allows it to adapt in various environments, influencing its solubility and reactivity in different biochemical contexts. | ||||||
Calcium phenylpyruvate | 51828-93-4 | sc-495877 sc-495877A | 1 g 5 g | $153.00 $462.00 | ||
Calcium phenylpyruvate showcases unique reactivity as a calcium salt, particularly through its ability to form chelates with metal ions, enhancing its solubility and stability in various environments. Its distinct structural features promote specific interactions with biological macromolecules, influencing metabolic pathways. The compound's role in facilitating electron transfer processes and its potential to stabilize reactive intermediates make it a noteworthy participant in diverse chemical transformations. | ||||||
di(Atorvastatin-d5) Calcium Salt | 222412-82-0 | sc-503150 sc-503150A | 500 µg 5 mg | $360.00 $2290.00 | ||
Di(Atorvastatin-d5) Calcium Salt is characterized by its unique isotopic labeling, which allows for precise tracking in biochemical pathways. The calcium salt form enhances its solubility and stability, facilitating interactions with biological membranes. Its distinct molecular structure promotes specific binding affinities, influencing cellular uptake and metabolic pathways. Additionally, the compound's reactivity is modulated by its calcium coordination, affecting its behavior in various chemical environments. | ||||||
DL-Gyceric Acid Calcium Salt | 67525-74-0 | sc-294396 sc-294396A | 250 mg 1 g | $75.00 $229.00 | ||
DL-Glyceric Acid Calcium Salt is notable for its dual functionality as both a calcium source and a carboxylic acid derivative. Its structure allows for effective coordination with calcium ions, promoting enhanced bioavailability. The compound's unique stereochemistry contributes to its reactivity, enabling it to engage in specific enzymatic pathways. Additionally, its hydrophilic nature aids in solvation, influencing its behavior in aqueous systems and facilitating interactions with various substrates. |