Items 1 to 10 of 185 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Methyl-β-cyclodextrin | 128446-36-6 | sc-215379A sc-215379 sc-215379C sc-215379B | 100 mg 1 g 10 g 5 g | $25.00 $65.00 $170.00 $110.00 | 19 | |
Methyl-β-cyclodextrin is a cyclic oligosaccharide known for its ability to form inclusion complexes with various hydrophobic molecules. Its unique toroidal structure allows for selective encapsulation, enhancing solubility and stability of guest compounds. The compound exhibits strong host-guest interactions, driven by hydrophobic effects and hydrogen bonding, which can influence reaction kinetics and molecular transport. Its ability to modulate the bioavailability of encapsulated substances highlights its significance in various chemical processes. | ||||||
FITC-Dextran 70 | 60842-46-8 | sc-263323 sc-263323A | 100 mg 500 mg | $140.00 $446.00 | 13 | |
FITC-Dextran 70 is a fluorescently labeled polysaccharide that exhibits unique properties due to its branched structure and high molecular weight. Its extensive hydroxyl groups facilitate strong hydrogen bonding and solvation, enhancing its interaction with biological membranes. The compound's size and hydrophilicity influence diffusion rates and permeability in various environments, making it a useful tool for studying molecular dynamics and transport mechanisms in complex systems. | ||||||
2-Chloro-4-nitrophenyl-α-D-glucopyranoside | 119047-14-2 | sc-220716 | 100 mg | $320.00 | ||
2-Chloro-4-nitrophenyl-α-D-glucopyranoside is a glycoside that showcases intriguing reactivity due to its chlorinated and nitro substituents. The electron-withdrawing nitro group enhances electrophilicity, facilitating nucleophilic attack in glycosylation reactions. Its unique structure allows for selective interactions with enzymes, influencing catalytic efficiency and substrate specificity. Additionally, the compound's solubility properties can be modulated by pH, affecting its behavior in various chemical environments. | ||||||
Heptakis(2,3-dimethyl)-β-cyclodextrin | 123155-05-5 | sc-396055 | 25 mg | $372.00 | ||
Heptakis(2,3-dimethyl)-β-cyclodextrin is a modified cyclic oligosaccharide characterized by its unique cavity structure, which allows for selective host-guest interactions. The presence of dimethyl groups enhances its solubility and alters its binding affinity for various guest molecules. This compound exhibits distinct molecular recognition capabilities, facilitating the formation of inclusion complexes that can influence reaction kinetics and stability in diverse chemical environments. Its unique conformation also affects its physical properties, such as viscosity and surface activity, making it an intriguing subject for studies on molecular encapsulation and transport phenomena. | ||||||
2′,2′-Difluoro-2′-deoxyuridine 3′,5′-Dibenzoate | 143157-27-1 | sc-396123 | 25 mg | $360.00 | ||
2′,2′-Difluoro-2′-deoxyuridine 3',5'-Dibenzoate is a modified nucleoside derivative that exhibits unique interactions due to its fluorinated structure. The presence of fluorine atoms enhances lipophilicity, influencing membrane permeability and molecular recognition. Its dibenzoate moiety contributes to distinct solubility characteristics and alters binding dynamics with biomolecules. This compound's reactivity and stability in various environments make it a fascinating subject for exploring nucleic acid interactions and enzymatic pathways. | ||||||
D-Erythrose 4-phosphate sodium salt | 103302-15-4 | sc-214801 sc-214801B sc-214801A sc-214801C | 5 mg 10 mg 25 mg 100 mg | $190.00 $307.00 $525.00 $1632.00 | 2 | |
D-Erythrose 4-phosphate sodium salt is a key intermediate in the pentose phosphate pathway, playing a crucial role in cellular metabolism. Its phosphate group enhances solubility and reactivity, allowing for efficient participation in enzymatic reactions. The compound's stereochemistry contributes to its specific interactions with enzymes, influencing reaction rates and product formation. Additionally, its ability to form stable complexes with metal ions can affect catalytic processes in biochemical pathways. | ||||||
Sucrose | 57-50-1 | sc-204311 sc-204311B sc-204311C sc-204311A | 0.5 kg 50 kg 100 kg 5 kg | $57.00 $1224.00 $1760.00 $195.00 | 6 | |
Sucrose is a disaccharide composed of glucose and fructose, linked by a glycosidic bond that influences its digestibility and sweetness. Its unique structure allows for specific interactions with enzymes like sucrase, facilitating hydrolysis into monosaccharides. This process is vital in energy metabolism. Sucrose's crystalline form exhibits hygroscopic properties, enabling it to attract moisture, which can impact its stability and behavior in various environments. | ||||||
rac-Glycerol 1-phosphate disodium salt hexahydrate | 34363-28-5 | sc-215789B sc-215789 sc-215789A | 1 g 5 g 25 g | $230.00 $410.00 $1450.00 | 3 | |
Rac-Glycerol 1-phosphate disodium salt hexahydrate is a versatile carbohydrate derivative characterized by its dual anionic nature, which enhances solubility and reactivity in aqueous environments. Its phosphate group plays a crucial role in metabolic pathways, acting as a key intermediate in lipid synthesis and energy production. The hexahydrate form contributes to its stability and influences its interaction with biomolecules, facilitating essential biochemical processes. | ||||||
(Hydroxypropyl)methyl cellulose | 9004-65-3 | sc-279197 sc-279197A sc-279197B | 50 g 250 g 1 kg | $65.00 $215.00 $500.00 | ||
(Hydroxypropyl)methyl cellulose is a cellulose ether distinguished by its unique hydrophilic properties, which enhance its ability to form gels and films in aqueous solutions. Its hydroxypropyl and methyl groups create a balance between hydrophilicity and hydrophobicity, influencing its viscosity and texture. This compound exhibits strong hydrogen bonding capabilities, allowing for effective stabilization of emulsions and suspensions, while also providing a barrier against moisture, enhancing its functional versatility. | ||||||
Trehalose, Dihydrate | 6138-23-4 | sc-202368 sc-202368A | 50 g 500 g | $147.00 $219.00 | 6 | |
Trehalose, Dihydrate is a disaccharide characterized by its non-reducing nature, which contributes to its stability in various environments. Its unique ability to form strong hydrogen bonds allows for effective hydration, protecting biomolecules from stress. The compound's dual glucose units enable it to participate in intricate metabolic pathways, influencing osmotic balance and cellular energy storage. Its crystalline structure also enhances its thermal stability, making it a resilient carbohydrate in diverse conditions. |