Sugar Alcohols
Items 61 to 65 of 65 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
allo-Inositol | 643-10-7 | sc-233831 | 25 mg | $53.00 | ||
Allo-Inositol, a stereoisomer of inositol, features a unique arrangement of hydroxyl groups that enables it to engage in specific hydrogen bonding interactions, enhancing its solubility in polar solvents. This compound participates in diverse metabolic pathways, influencing cellular signaling and energy regulation. Its distinct stereochemistry allows for selective interactions with enzymes and receptors, potentially modulating biochemical processes. Additionally, its capacity to form stable complexes with metal ions can alter its reactivity and stability in various environments. | ||||||
DL-Arabitol | 6018-27-5 | sc-285464 sc-285464A | 50 mg 100 mg | $162.00 $232.00 | ||
DL-Arabitol is a sugar alcohol characterized by its unique stereochemistry, which allows for multiple hydroxyl groups to participate in hydrogen bonding, enhancing its solubility in aqueous environments. This compound undergoes fermentation pathways, where it can be metabolized by specific microorganisms, influencing the production of various metabolites. Its ability to form stable complexes with other biomolecules can affect its reactivity and interactions in biological systems, showcasing its versatility in biochemical contexts. | ||||||
Inositol | 6917-35-7 | sc-394417 | 100 g | $77.00 | ||
Inositol is a cyclic sugar alcohol notable for its role in cellular signaling and osmoregulation. Its six-membered ring structure allows for multiple hydroxyl groups, facilitating strong hydrogen bonding and enhancing its solubility in polar solvents. Inositol participates in various metabolic pathways, influencing lipid metabolism and cellular communication. Its unique configuration enables it to interact with phospholipids, impacting membrane dynamics and cellular function. | ||||||
muco-Inositol | 41546-34-3 | sc-295506 | 100 mg | $700.00 | ||
Muco-Inositol is a stereoisomer of inositol characterized by its distinct arrangement of hydroxyl groups, which influences its reactivity and solubility. This compound exhibits unique molecular interactions, particularly through its ability to form stable complexes with metal ions, enhancing its role in biochemical pathways. Its structural properties allow for efficient participation in carbohydrate metabolism, contributing to energy production and cellular homeostasis. | ||||||
[1-13Cgal]Lactose monohydrate | 64044-51-5 (unlabeled) | sc-495618 | 2.5 mg | $300.00 | ||
[1-13Cgal]Lactose monohydrate is a stable disaccharide that features a unique carbon isotope, enhancing its traceability in metabolic studies. This compound participates in specific enzymatic reactions, particularly in the lactase pathway, where its distinct isotopic labeling allows for detailed tracking of carbohydrate absorption and fermentation processes. Its hygroscopic nature contributes to its solubility, facilitating interactions in various biochemical environments. | ||||||