Items 161 to 170 of 214 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Maltopentaose | 34620-76-3 | sc-218666C sc-218666 sc-218666A sc-218666D sc-218666E sc-218666B | 25 mg 50 mg 100 mg 250 mg 500 mg 1 g | $236.00 $409.00 $649.00 $1199.00 $2299.00 $3349.00 | 1 | |
Maltopentaose is a linear oligosaccharide composed of five glucose units linked by α-1,4-glycosidic bonds. Its unique structure allows for specific interactions with enzymes, facilitating its breakdown into simpler sugars during digestion. The presence of multiple hydroxyl groups enhances its solubility in water, promoting hydrogen bonding with surrounding molecules. This property influences its behavior in various biochemical pathways, particularly in energy metabolism and fermentation processes. | ||||||
Digalacturonic acid | 5894-59-7 | sc-214891 sc-214891A sc-214891B | 10 mg 25 mg 100 mg | $148.00 $255.00 $823.00 | 2 | |
Digalacturonic acid is a polysaccharide characterized by its unique galacturonic acid units linked through α-1,4-glycosidic bonds. This structure enables it to form gel-like networks in aqueous environments, enhancing its viscosity and stability. Its carboxyl groups engage in ionic interactions, influencing its solubility and reactivity in various biochemical processes. Additionally, it plays a role in plant cell wall integrity, impacting cellular interactions and structural properties. | ||||||
Erlose | 13101-54-7 | sc-214968A sc-214968 sc-214968B sc-214968C | 10 mg 50 mg 100 mg 250 mg | $128.00 $332.00 $602.00 $1128.00 | 2 | |
Erlose is a polysaccharide distinguished by its intricate branching structure, which facilitates diverse molecular interactions. Its unique configuration allows for the formation of hydrogen bonds, contributing to its solubility and gel-forming capabilities. The presence of multiple hydroxyl groups enhances its hygroscopic nature, enabling it to retain moisture effectively. This polysaccharide also exhibits distinct rheological properties, influencing flow behavior in various environments. | ||||||
Xanthan gum | 11138-66-2 | sc-296703 sc-296703A | 100 g 500 g | $82.00 $275.00 | ||
Xanthan gum is a polysaccharide characterized by its high molecular weight and unique helical structure, which promotes strong intermolecular interactions. Its anionic nature allows for electrostatic interactions with cations, enhancing its thickening properties. Xanthan gum exhibits shear-thinning behavior, making it ideal for applications requiring viscosity changes under stress. Additionally, its ability to form stable gels in the presence of various salts highlights its versatility in diverse formulations. | ||||||
Tragacanth | 9000-65-1 | sc-215995 sc-215995A | 100 g 500 g | $71.00 $228.00 | 1 | |
Tragacanth is a complex polysaccharide derived from the sap of certain plants, notable for its unique branched structure that contributes to its gel-forming capabilities. It exhibits a high degree of water solubility, leading to the formation of viscous solutions. The presence of various functional groups allows for hydrogen bonding and interactions with water molecules, enhancing its thickening and stabilizing properties. Tragacanth's ability to create stable emulsions and foams makes it a versatile ingredient in various formulations. | ||||||
4-O-β-Galactopyranosyl-D-mannopyranose | 20869-27-6 | sc-220989 sc-220989A | 25 mg 100 mg | $194.00 $418.00 | ||
4-O-β-Galactopyranosyl-D-mannopyranose is a unique polysaccharide characterized by its specific glycosidic linkages, which influence its solubility and reactivity. This compound exhibits distinct molecular interactions, particularly through hydrogen bonding, which enhances its ability to form hydrogels. Its structural configuration allows for selective binding with other biomolecules, potentially affecting reaction kinetics and stability in various environments. The compound's physical properties, such as viscosity and texture, are influenced by its molecular weight and branching, making it an intriguing subject for further study in polysaccharide behavior. | ||||||
6-O-alpha-D-Glucosyl-beta-cyclodextrin | 92517-02-7 | sc-291408 sc-291408A | 1 g 5 g | $215.00 $315.00 | ||
6-O-alpha-D-Glucosyl-beta-cyclodextrin is a distinctive polysaccharide known for its unique cyclic structure, which facilitates the formation of inclusion complexes with various guest molecules. This compound exhibits remarkable solubility in water, attributed to its hydrophilic exterior and hydrophobic cavity, enabling selective molecular encapsulation. Its ability to modulate reaction kinetics through host-guest interactions and its impact on viscosity and gel formation make it a fascinating subject for exploration in polysaccharide chemistry. | ||||||
Gum storax | 8046-19-3 | sc-215119 | 100 g | $180.00 | ||
Gum storax is a complex polysaccharide characterized by its rich aromatic profile and viscous nature. It exhibits unique intermolecular interactions, forming gels and emulsions that enhance stability in various environments. The presence of specific functional groups allows for hydrogen bonding and hydrophobic interactions, influencing its rheological properties. Additionally, gum storax's ability to interact with water molecules contributes to its thickening and film-forming capabilities, making it an intriguing subject in material science. | ||||||
Glycol chitosan | 123938-86-3 | sc-215100 sc-215100A sc-215100B | 500 mg 1 g 5 g | $79.00 $109.00 $369.00 | 1 | |
Glycol chitosan is a versatile polysaccharide known for its unique solubility and gel-forming properties. Its structure allows for strong hydrogen bonding and electrostatic interactions, which enhance its stability in aqueous solutions. The presence of hydroxyl and amino groups facilitates complexation with metal ions, influencing its behavior in various chemical environments. Additionally, glycol chitosan exhibits shear-thinning behavior, making it suitable for applications requiring adjustable viscosity. | ||||||
D-(+)-Sucrose octaacetate | 126-14-7 | sc-257278 sc-257278A | 250 g 1 kg | $49.00 $136.00 | ||
D-(+)-Sucrose octaacetate is a distinctive polysaccharide derivative characterized by its extensive acetylation, which significantly alters its solubility and reactivity. The presence of multiple acetyl groups enhances its hydrophobic interactions, leading to unique aggregation behaviors in solution. This compound exhibits selective binding properties, allowing it to interact with specific biomolecules. Its structural configuration also influences its thermal stability and reactivity in various chemical pathways, making it an intriguing subject for further study. |