Amino Alcohols
Items 1 to 10 of 491 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
DL-threo-Dihydrosphingosine | 73938-69-9 | sc-201389 | 10 mg | $190.00 | 1 | |
DL-threo-Dihydrosphingosine is characterized by its dual amino alcohol structure, which facilitates unique hydrogen bonding and hydrophilic interactions. This compound plays a crucial role in sphingolipid metabolism, influencing membrane fluidity and cellular signaling pathways. Its ability to form stable complexes with lipid bilayers enhances its integration into cellular membranes, impacting lipid raft formation and protein interactions. Additionally, its stereochemistry contributes to distinct reactivity profiles in biochemical pathways. | ||||||
D-erythro-Sphingosine-1-phosphate | 26993-30-6 | sc-201383 sc-201383D sc-201383A sc-201383B sc-201383C | 1 mg 2 mg 5 mg 10 mg 25 mg | $162.00 $316.00 $559.00 $889.00 $1693.00 | 7 | |
D-erythro-Sphingosine-1-phosphate is a bioactive sphingolipid that exhibits unique amphiphilic properties, allowing it to interact favorably with both hydrophilic and hydrophobic environments. This compound is integral to cellular signaling, particularly in regulating cytoskeletal dynamics and cell migration. Its specific stereochemistry influences receptor binding affinities, modulating downstream signaling cascades. Furthermore, it participates in lipid metabolism, impacting membrane composition and cellular homeostasis. | ||||||
ICI 89406 | 53671-71-9 | sc-361212 sc-361212A | 10 mg 50 mg | $91.00 $520.00 | 1 | |
ICI 89406 is a distinctive amino alcohol characterized by its ability to form strong hydrogen bonds, enhancing its solubility in polar solvents. This compound exhibits unique reactivity patterns, particularly in nucleophilic substitution reactions, where its amino group can act as a nucleophile. Its structural features facilitate specific interactions with metal ions, potentially influencing catalytic pathways. Additionally, ICI 89406's chiral centers contribute to its stereochemical diversity, affecting its reactivity and interaction profiles in various chemical environments. | ||||||
N,N,N′,N′-Tetrakis(2-hydroxypropyl)ethylenediamine | 102-60-3 | sc-255375 sc-255375A | 100 g 500 g | $35.00 $77.00 | ||
N,N,N',N'-Tetrakis(2-hydroxypropyl)ethylenediamine is a versatile amino alcohol known for its exceptional chelating properties, allowing it to form stable complexes with transition metals. Its multiple hydroxyl groups enhance its capacity for hydrogen bonding, leading to increased viscosity in solution. The compound's unique branched structure promotes steric hindrance, influencing reaction kinetics and selectivity in various chemical transformations, making it a key player in coordination chemistry. | ||||||
Ethanolamine | 141-43-5 | sc-203042 sc-203042A sc-203042B | 25 ml 500 ml 2.5 L | $21.00 $55.00 $200.00 | 1 | |
Ethanolamine is a unique amino alcohol characterized by its dual functional groups, which enable it to engage in both hydrogen bonding and nucleophilic reactions. This compound exhibits a strong affinity for carbonyl compounds, facilitating the formation of stable intermediates in various organic reactions. Its polar nature enhances solubility in water and organic solvents, while its ability to act as a base allows for participation in acid-base reactions, influencing reaction pathways and kinetics. | ||||||
6-Hydroxydopamine hydrobromide | 636-00-0 | sc-256988 sc-256988A | 50 mg 250 mg | $92.00 $245.00 | 5 | |
6-Hydroxydopamine hydrobromide is an amino alcohol distinguished by its catechol structure, which allows for extensive hydrogen bonding and electron delocalization. This compound exhibits unique reactivity with electrophiles, promoting the formation of diverse adducts. Its hydroxyl groups enhance solubility in polar solvents, while its ability to undergo oxidation and polymerization reactions contributes to its complex behavior in various chemical environments. | ||||||
(R)-(+)-Atenolol | 56715-13-0 | sc-236603 | 100 mg | $157.00 | 1 | |
(R)-(+)-Atenolol is an amino alcohol characterized by its chiral center, which influences its stereochemistry and molecular interactions. The presence of hydroxyl and amine groups facilitates strong hydrogen bonding, enhancing its solubility in polar media. This compound can participate in nucleophilic reactions, showcasing distinct reactivity patterns. Its unique spatial arrangement also affects its interaction with other molecules, leading to varied kinetic profiles in chemical processes. | ||||||
Carvedilol | 72956-09-3 | sc-200157 sc-200157A sc-200157B sc-200157C sc-200157D | 100 mg 1 g 10 g 25 g 100 g | $122.00 $235.00 $520.00 $979.00 $1500.00 | 2 | |
Carvedilol is an amino alcohol distinguished by its dual functional groups, which enable diverse intermolecular interactions. The compound's unique stereochemistry allows for specific conformational flexibility, influencing its reactivity in various chemical environments. Its ability to form robust hydrogen bonds enhances solvation dynamics, while the presence of aromatic rings contributes to π-π stacking interactions. These characteristics result in distinctive reaction kinetics and pathways, making it a versatile participant in organic synthesis. | ||||||
BIS-Tris | 6976-37-0 | sc-216088 sc-216088A sc-216088B | 100 g 500 g 1 kg | $76.00 $195.00 $405.00 | 4 | |
BIS-Tris is an amino alcohol characterized by its three hydroxymethyl groups, which facilitate strong hydrogen bonding and enhance solubility in aqueous environments. Its unique structure allows for effective buffering capacity across a range of pH levels, promoting stability in biochemical reactions. The compound's ability to form stable complexes with metal ions and other biomolecules further influences its reactivity, making it a key player in various chemical processes. | ||||||
(S)-(-)-Methioninol | 2899-37-8 | sc-255554 | 1 g | $88.00 | ||
(S)-(-)-Methioninol is an amino alcohol distinguished by its chiral center and sulfur-containing side chain, which contribute to its unique stereochemistry and reactivity. This compound exhibits notable hydrogen bonding capabilities, enhancing its solubility in polar solvents. Its structure allows for specific interactions with proteins and enzymes, potentially influencing catalytic pathways. Additionally, the presence of the thiol group can participate in redox reactions, adding to its versatility in various chemical environments. | ||||||