Items 181 to 190 of 214 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Hydroxypropyl starch | 9049-76-7 | sc-353626 sc-353626A | 25 g 100 g | $104.00 $306.00 | 2 | |
Hydroxypropyl starch is a modified polysaccharide known for its unique hydrophilic properties, resulting from the introduction of hydroxypropyl groups. This modification enhances its solubility in water and improves its film-forming capabilities. The presence of hydroxypropyl groups alters the starch's molecular interactions, leading to increased viscosity and stability in various formulations. Its distinct structural characteristics enable it to form gels and emulsions, influencing texture and mouthfeel in diverse applications. | ||||||
α-Lactose monohydrate | 5989-81-1 | sc-221188 sc-221188A | 10 mg 1 kg | $36.00 $126.00 | 1 | |
α-Lactose monohydrate is a disaccharide that exhibits unique hygroscopic properties, allowing it to absorb moisture from the environment. This characteristic influences its crystallization behavior and stability in various formulations. The presence of hydroxyl groups facilitates hydrogen bonding, enhancing its solubility and interaction with other molecules. Additionally, its crystalline structure contributes to a distinct sweetness profile and influences the texture of food products, making it a versatile ingredient in various formulations. | ||||||
Triacetyl-β-cyclodextrin | 23739-88-0 | sc-237245 | 10 g | $126.00 | ||
Triacetyl-β-cyclodextrin is a modified polysaccharide characterized by its unique cyclic structure, which facilitates the formation of inclusion complexes with various guest molecules. This property arises from its hydrophilic exterior and hydrophobic cavity, enabling selective molecular encapsulation. The compound exhibits enhanced solubility in organic solvents and demonstrates distinct thermal stability. Its ability to form stable complexes can influence reaction kinetics and molecular interactions, making it a versatile agent in various chemical processes. | ||||||
Maltooctaose | 66567-45-1 | sc-286149 sc-286149A | 100 mg 250 mg | $276.00 $456.00 | ||
Maltooctaose is a polysaccharide composed of multiple glucose units linked by α-1,4 glycosidic bonds, showcasing unique structural properties that influence its solubility and viscosity. Its branched configuration allows for extensive hydrogen bonding, enhancing its interaction with water and other polysaccharides. This results in a gel-like consistency in solution, which can affect texture and mouthfeel in various applications. Additionally, its molecular weight contributes to its stability and resistance to enzymatic degradation. | ||||||
Heparin disaccharide IV-S, sodium Salt | 136098-08-3 | sc-391190 sc-391190A | 1 mg 2 mg | $390.00 $693.00 | ||
Heparin disaccharide IV-S, sodium salt, is a highly sulfated polysaccharide known for its intricate molecular structure that promotes strong electrostatic interactions with proteins and other biomolecules. This compound exhibits unique conformational flexibility, allowing it to engage in specific binding with various targets. Its high negative charge density enhances its solubility in aqueous environments, influencing diffusion rates and reaction dynamics in biochemical pathways. | ||||||
Sephadex LH-20 | 9041-37-6 | sc-471537 sc-471537A sc-471537B | 25 g 100 g 500 g | $270.00 $724.00 $3325.00 | 1 | |
Sephadex LH-20 is a dextran-based polysaccharide characterized by its porous structure, which facilitates selective molecular sieving. Its unique hydrophilic nature allows for effective interactions with a wide range of solutes, promoting differential adsorption based on size and shape. The material exhibits a high degree of swelling in aqueous solutions, enhancing its capacity for separation processes. Additionally, its tunable pore size enables tailored applications in various chromatographic techniques. | ||||||
D-(+)-Cellohexose | 2478-35-5 | sc-221461A sc-221461B sc-221461 sc-221461C sc-221461D sc-221461E | 1 mg 2 mg 5 mg 10 mg 25 mg 50 mg | $180.00 $240.00 $380.00 $573.00 $1240.00 $2290.00 | ||
D-(+)-Cellohexose is a polysaccharide composed of glucose units linked by β-1,4-glycosidic bonds, forming a linear chain that exhibits strong hydrogen bonding capabilities. This structure contributes to its high crystallinity and stability, influencing its solubility and reactivity in various environments. The polymer's ability to form gels and films is notable, allowing for unique interactions with water and other molecules, which can affect its behavior in biochemical pathways and material science applications. | ||||||
Lactose Octaacetate | 6291-42-5 | sc-221829 | 25 g | $228.00 | ||
Lactose Octaacetate is a polysaccharide derivative characterized by its extensive acetylation, which enhances its hydrophobic properties and alters its solubility profile. This modification leads to unique molecular interactions, particularly in forming stable complexes with other biomolecules. The compound exhibits distinct reaction kinetics, often undergoing hydrolysis in aqueous environments, which can influence its behavior in various chemical processes. Its structural flexibility allows for diverse conformations, impacting its physical properties and interactions in complex systems. | ||||||
Verbascose | 546-62-3 | sc-253826 | 5 mg | $90.00 | ||
Verbascose is a complex polysaccharide composed of galactose and glucose units, notable for its unique branching structure that influences its solubility and viscosity in aqueous solutions. This branching facilitates specific intermolecular interactions, enhancing its ability to form gels and stabilize emulsions. The compound exhibits distinct rheological properties, making it a subject of interest in studies of carbohydrate behavior under varying shear conditions. Its molecular architecture also affects its degradation pathways, influencing its stability and reactivity in different environments. | ||||||
4-Galactosyllactose | 6587-31-1 | sc-284244 sc-284244A | 1 mg 2 mg | $204.00 $306.00 | ||
4-Galactosyllactose is a polysaccharide characterized by its unique linear and branched configurations, which contribute to its distinctive solubility and gel-forming capabilities. The presence of multiple galactose units enhances hydrogen bonding interactions, leading to increased viscosity in solution. Its structural diversity allows for varied enzymatic degradation pathways, influencing its reactivity and stability in different conditions. This compound's molecular interactions play a crucial role in its behavior in complex carbohydrate systems. |