Items 61 to 70 of 185 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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1-Hydroxypyrene-d9 | 132603-37-3 | sc-213342 sc-213342A | 10 mg 50 mg | $360.00 $980.00 | ||
1-Hydroxypyrene-d9, a polycyclic aromatic hydrocarbon, showcases intriguing molecular interactions that influence its behavior in various environments. Its unique structure allows for effective π-π stacking and hydrophobic interactions, enhancing its solubility in organic solvents. The compound's isotopic labeling facilitates tracking in environmental studies, while its reactivity with electrophiles can lead to distinct pathways in photochemical processes, impacting reaction rates and product formation. | ||||||
Sucrose 6′-Acetate | 936001-72-8 | sc-220147 | 500 mg | $360.00 | ||
Sucrose 6'-Acetate is a modified carbohydrate that showcases unique esterification properties, enhancing its hydrophobic character. This modification alters its interaction with water, leading to distinct solubility profiles. The presence of acetyl groups influences its reactivity in glycosylation processes, allowing for selective binding in enzymatic reactions. Additionally, its structural conformation can affect molecular recognition, impacting its behavior in various biochemical contexts. | ||||||
D-myo-Inositol-2,4-diphosphate (sodium salt) | sc-221509 sc-221509A | 100 µg 500 µg | $78.00 $352.00 | |||
D-myo-Inositol-2,4-diphosphate (sodium salt) is a phosphoinositide derivative that plays a pivotal role in cellular signaling pathways. Its diphosphate groups facilitate interactions with specific proteins, influencing signal transduction mechanisms. The compound exhibits unique binding affinities, modulating enzyme activity and cellular responses. Its structural configuration allows for distinct conformational changes, impacting its reactivity and interactions within biological systems, thereby influencing metabolic processes. | ||||||
D-myo-Inositol-3,4,5,6-tetraphosphate (sodium salt) | sc-221513 sc-221513A | 100 µg 500 µg | $165.00 $744.00 | |||
D-myo-Inositol-3,4,5,6-tetraphosphate (sodium salt) is a polyphosphate carbohydrate that participates in intricate cellular signaling networks. Its multiple phosphate groups enable it to engage in specific ionic interactions, enhancing its affinity for various proteins and receptors. This compound is involved in regulating calcium signaling and modulating cellular responses through its unique ability to form stable complexes. Its structural versatility allows for dynamic conformational shifts, influencing its reactivity and interactions in metabolic pathways. | ||||||
D-myo-Inositol-1,3,4,5,6-pentaphosphate, sodium salt | sc-223921 sc-223921A | 100 µg 500 µg | $100.00 $294.00 | |||
D-myo-Inositol-1,3,4,5,6-pentaphosphate, sodium salt, is a complex carbohydrate characterized by its high degree of phosphorylation, which facilitates unique interactions with metal ions and proteins. This compound plays a crucial role in cellular energy metabolism and signal transduction, acting as a key regulator in various biochemical pathways. Its intricate structure allows for diverse conformational states, enhancing its reactivity and enabling it to participate in multiple cellular processes. | ||||||
Poly-beta-cyclodextrin [Cross-linked by Epichlorohydrin] | sc-296103 sc-296103A | 1 g 5 g | $150.00 $400.00 | 1 | ||
Poly-beta-cyclodextrin, cross-linked by epichlorohydrin, is a modified carbohydrate characterized by its unique cyclic structure and enhanced stability. This compound exhibits remarkable host-guest chemistry, allowing it to encapsulate various guest molecules through non-covalent interactions. Its cross-linked nature imparts increased mechanical strength and resistance to degradation, while its hydrophilic exterior promotes solubility in aqueous environments, facilitating diverse applications in material science and environmental chemistry. | ||||||
D(+)Glucosamine, Hydrochloride | 66-84-2 | sc-211202 sc-211202A sc-211202B | 100 g 1 kg 10 kg | $50.00 $120.00 $950.00 | ||
D(+)Glucosamine Hydrochloride is a naturally occurring amino sugar that plays a pivotal role in the synthesis of glycosaminoglycans, essential components of connective tissues. Its unique structure allows for specific hydrogen bonding and electrostatic interactions, enhancing its solubility in aqueous solutions. This compound participates in various metabolic pathways, influencing cellular signaling and structural integrity, while its hygroscopic nature contributes to moisture retention in biological systems. | ||||||
Maltitol | 585-88-6 | sc-215287 sc-215287A | 25 g 100 g | $59.00 $190.00 | ||
Maltitol is a sugar alcohol derived from maltose, characterized by its ability to mimic the sweetness of sucrose while exhibiting lower caloric content. Its unique polyol structure allows for hydrogen bonding with water molecules, enhancing its solubility and contributing to its smooth texture in formulations. Maltitol undergoes fermentation by gut bacteria, leading to distinct metabolic pathways that can influence osmotic balance in the digestive system. Its crystalline form provides stability and a pleasant mouthfeel, making it a popular choice in various applications. | ||||||
D-(+)-Melibiose Monohydrate | 585-99-9 | sc-294150 sc-294150A | 1 g 10 g | $42.00 $146.00 | 2 | |
D-(+)-Melibiose Monohydrate is a disaccharide composed of glucose and galactose, notable for its role in carbohydrate metabolism. It exhibits unique interactions with enzymes, particularly in the context of glycosidic bond hydrolysis, influencing reaction kinetics in various biological pathways. Its hydrophilic nature enhances solubility in aqueous environments, facilitating its participation in fermentation processes. The compound's crystalline structure contributes to its stability and texture, making it an interesting subject for studies on carbohydrate behavior. | ||||||
6-O-α-Maltosyl-β-cyclodextrin | 104723-60-6 | sc-214380 | 5 g | $168.00 | ||
6-O-α-Maltosyl-β-cyclodextrin is a modified cyclodextrin that exhibits unique host-guest chemistry due to its cyclic structure and multiple hydroxyl groups. This compound can encapsulate hydrophobic molecules, enhancing their solubility and stability. Its ability to form inclusion complexes is influenced by the size and shape of the guest molecules, leading to distinct reaction kinetics. The carbohydrate's solubility and viscosity properties are also notable, making it a versatile component in various applications. |