Items 131 to 140 of 214 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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κ-Carrageenan | 11114-20-8 | sc-213226 | 25 g | $82.00 | ||
κ-Carrageenan is a linear polysaccharide composed of repeating disaccharide units, which allows it to adopt various helical conformations. This structural versatility facilitates strong intermolecular interactions, particularly through hydrogen bonding and ionic interactions with cations. Its gelation properties are influenced by the presence of sulfate groups, which enhance its viscosity and stability in solution. The unique molecular arrangement also affects its rheological behavior, making it responsive to shear and temperature changes. | ||||||
Heparin disaccharide II-S sodium salt | 136098-05-0 | sc-215134 sc-215134A | 500 µg 1 mg | $389.00 $633.00 | ||
Heparin disaccharide II-S sodium salt is a highly sulfated polysaccharide characterized by its unique disaccharide structure, which promotes specific molecular interactions, including electrostatic and hydrophobic forces. Its extensive sulfation pattern enhances solubility and contributes to its ability to form stable complexes with various biomolecules. The compound exhibits distinct viscoelastic properties, allowing it to respond dynamically to changes in environmental conditions, such as pH and ionic strength. | ||||||
Maltose solution | 69-79-4 | sc-215288 | 100 ml | $112.00 | ||
Maltose solution is a disaccharide composed of two glucose units linked by an α(1→4) glycosidic bond, showcasing unique molecular interactions that facilitate hydrogen bonding and solubility in water. Its structure allows for efficient enzymatic hydrolysis, leading to rapid glucose release, which is crucial in metabolic pathways. The solution exhibits a sweet taste and contributes to the osmotic balance in various systems, influencing reaction kinetics and stability in carbohydrate chemistry. | ||||||
D-Maltose, Monohydrate | 6363-53-7 | sc-280954 | 100 g | $58.00 | ||
D-Maltose, Monohydrate is a disaccharide that exhibits unique hygroscopic properties, allowing it to attract and retain moisture, which can influence its stability and behavior in various environments. Its molecular structure facilitates specific hydrogen bonding interactions, enhancing solubility in aqueous solutions. This compound also participates in Maillard reactions, contributing to browning and flavor development in food systems, showcasing its role in complex biochemical pathways. | ||||||
β-Gentiobiose octaacetate | 4613-78-9 | sc-284977 sc-284977A | 10 g 25 g | $500.00 $1000.00 | ||
β-Gentiobiose octaacetate is a complex polysaccharide derivative characterized by its extensive acetylation, which enhances its hydrophobic properties and alters its solubility profile. This modification influences intermolecular interactions, promoting unique aggregation behaviors in solution. The compound exhibits distinct reactivity patterns, particularly in esterification reactions, where its bulky acetyl groups can hinder access to reactive sites, affecting reaction kinetics and selectivity in synthetic pathways. | ||||||
N-Linked Oligosaccharide, Man-9 Glycan | 71246-55-4 | sc-222008 | 20 µg | $1380.00 | ||
N-Linked Oligosaccharide, Man-9 Glycan, is a complex polysaccharide characterized by its intricate branching structure, which plays a crucial role in cellular recognition and signaling. Its unique configuration allows for specific interactions with lectins and receptors, influencing various biological processes. The glycan's stability in diverse pH environments and its ability to modulate protein folding and stability highlight its significance in glycoprotein biosynthesis and cellular communication pathways. | ||||||
Gal1-β-4GlcNAc1-β-6Gal | 20331-45-7 | sc-221647 | 1 mg | $380.00 | ||
Gal1-β-4GlcNAc1-β-6Gal is a complex polysaccharide distinguished by its unique glycosidic linkages, which facilitate specific molecular interactions essential for cellular adhesion and recognition. Its structural diversity enables it to participate in intricate signaling pathways, influencing cellular responses. The polysaccharide exhibits remarkable stability under varying ionic conditions, enhancing its role in modulating interactions with proteins and other biomolecules, thereby impacting cellular dynamics. | ||||||
N,N′-Diacetylchitobiose | 35061-50-8 | sc-219291 sc-219291A | 10 mg 50 mg | $252.00 $1056.00 | ||
N,N'-Diacetylchitobiose is a disaccharide composed of two N-acetylglucosamine units linked by β-1,4-glycosidic bonds. This structure allows for specific hydrogen bonding and hydrophobic interactions, contributing to its solubility and stability in aqueous environments. Its unique conformation can influence enzyme binding and substrate specificity, playing a role in various biochemical pathways. Additionally, it exhibits distinct thermal and mechanical properties, making it an interesting subject for studies on polysaccharide behavior. | ||||||
Agarose LE (low electroendosmosis) | 9012-36-6 | sc-286959A sc-286959 sc-286959B | 100 g 500 g 1 kg | $129.00 $512.00 $820.00 | ||
Agarose LE is a linear polysaccharide derived from agar, characterized by its low electroendosmosis properties. This unique feature enhances its gel-forming ability, allowing for precise control over pore size and mechanical strength in gel matrices. The molecular structure promotes specific hydrogen bonding and hydrophilic interactions, influencing its viscosity and gelation kinetics. Its distinct physical properties make it suitable for applications requiring high resolution and stability in various environments. | ||||||
4-O-(α-D-Mannopyranosyl)-D-mannose | 35438-40-5 | sc-284423 sc-284423A | 5 mg 10 mg | $128.00 $300.00 | ||
4-O-(α-D-Mannopyranosyl)-D-mannose is a branched polysaccharide notable for its unique glycosidic linkages, which facilitate specific molecular recognition and interaction with other biomolecules. Its structure allows for enhanced solubility and stability in aqueous environments, influencing its behavior in various biochemical pathways. The compound exhibits distinct rheological properties, contributing to its ability to form dynamic networks that respond to changes in concentration and temperature, making it a versatile component in polysaccharide chemistry. |