Items 51 to 60 of 491 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Oxolamine citrate salt | 1949-20-8 | sc-236263 | 25 g | $83.00 | ||
Oxolamine citrate salt, an amino alcohol, features a unique dual functional group that facilitates diverse molecular interactions. Its hydroxyl group enables robust hydrogen bonding, while the citrate moiety introduces additional ionic interactions, enhancing solubility in aqueous environments. This compound can engage in complexation with metal ions, influencing reaction kinetics and selectivity. Its structural attributes allow for participation in both acid-base and redox reactions, showcasing its multifaceted reactivity in synthetic applications. | ||||||
Sotalol hydrochloride | 959-24-0 | sc-203699 sc-203699A | 10 mg 50 mg | $67.00 $246.00 | 3 | |
Sotalol hydrochloride, as an amino alcohol, features a unique chiral center that facilitates specific stereochemical interactions, enhancing its reactivity in asymmetric synthesis. The presence of the hydroxyl group allows for robust hydrogen bonding, which can stabilize transition states during reactions. Additionally, its dual amine functionality enables diverse coordination with metal ions, potentially influencing catalytic pathways and reaction kinetics in complex systems. | ||||||
Ethanolamine hydrochloride | 2002-24-6 | sc-326924 sc-326924A | 25 g 100 g | $31.00 $51.00 | ||
Ethanolamine hydrochloride, an amino alcohol, exhibits intriguing properties due to its primary amine and hydroxyl groups, which promote strong hydrogen bonding and dipole-dipole interactions. This compound can act as a versatile ligand, forming stable complexes with various metal ions, thereby influencing catalytic pathways. Its ionic nature enhances solubility in polar solvents, facilitating its role in diverse chemical reactions, including nucleophilic substitutions and condensation processes. | ||||||
2-Butyl-1-octanol | 3913-02-8 | sc-230097 | 100 ml | $89.00 | ||
2-Butyl-1-octanol, classified as an amino alcohol, features a long hydrocarbon chain that enhances its hydrophobic interactions, promoting solubility in non-polar environments. The presence of the hydroxyl group enables strong hydrogen bonding, which can stabilize transition states during reactions. This compound's unique structure allows for selective reactivity in nucleophilic addition processes, making it a key player in various organic synthesis pathways. Its branched nature also influences steric effects, impacting reaction kinetics. | ||||||
5-Amino-1-pentanol | 2508-29-4 | sc-239022 | 10 g | $52.00 | 1 | |
5-Amino-1-pentanol, classified as an amino alcohol, features a unique structure that allows for significant steric hindrance and molecular flexibility. The presence of both an amino group and a hydroxyl group enables it to engage in robust hydrogen bonding, enhancing its reactivity in condensation reactions. Its ability to act as a nucleophile is influenced by the electron-donating nature of the amino group, which can stabilize transition states in various organic transformations. Additionally, its hydrophilic character promotes solubility in aqueous environments, making it a key player in diverse chemical syntheses. | ||||||
5-Benzyloxy-1-pentanol | 4541-15-5 | sc-233250 | 5 ml | $117.00 | ||
5-Benzyloxy-1-pentanol, an amino alcohol, exhibits intriguing properties due to its benzyloxy group, which enhances its electron-donating ability. This feature facilitates unique molecular interactions, particularly in hydrogen bonding and dipole-dipole interactions, influencing its reactivity in condensation reactions. The compound's moderate polarity allows it to engage in both polar and non-polar environments, affecting solubility and reaction pathways. Its structural characteristics also contribute to distinct steric effects, impacting the kinetics of various chemical transformations. | ||||||
L-Tryptophanol | 2899-29-8 | sc-255247 | 1 g | $95.00 | ||
L-Tryptophanol, an amino alcohol, exhibits intriguing molecular characteristics due to its indole structure, which contributes to unique π-π stacking interactions. This aromatic system enhances its reactivity in electrophilic substitution reactions. The hydroxyl group facilitates intramolecular hydrogen bonding, influencing conformational dynamics and reaction pathways. Its dual functionality allows it to participate in diverse chemical transformations, showcasing versatility in synthetic applications. | ||||||
5-Hydroxydopamine hydrochloride | 5720-26-3 | sc-233375 sc-233375A sc-233375B sc-233375C sc-233375D sc-233375E sc-233375F | 100 mg 500 mg 1 g 5 g 10 g 50 g 100 g | $87.00 $393.00 $648.00 $1922.00 $3198.00 $9700.00 $11230.00 | ||
5-Hydroxydopamine hydrochloride, classified as an amino alcohol, showcases remarkable reactivity due to its hydroxyl and amino functional groups. These groups enable strong hydrogen bonding, enhancing solubility in polar solvents and influencing its interaction with biomolecules. The compound's unique structural arrangement allows for specific conformational changes, which can affect its participation in enzymatic reactions and alter reaction kinetics. Its ability to form stable complexes with metal ions further diversifies its chemical behavior. | ||||||
1,3-Bis(dimethylamino)-2-propanol | 5966-51-8 | sc-222925 | 10 g | $169.00 | ||
1,3-Bis(dimethylamino)-2-propanol, an amino alcohol, exhibits intriguing properties due to its dual amino groups, which facilitate robust intramolecular hydrogen bonding. This unique feature enhances its nucleophilicity, allowing it to engage in diverse reaction pathways. The compound's steric configuration influences its reactivity, promoting selective interactions with electrophiles. Additionally, its polar nature contributes to significant solvation effects, impacting reaction kinetics and stability in various environments. | ||||||
Meglumine | 6284-40-8 | sc-205383 sc-205383A sc-205383B sc-205383C | 50 g 250 g 500 g 1 kg | $50.00 $89.00 $140.00 $280.00 | ||
Meglumine, an amino alcohol, showcases distinctive characteristics stemming from its polyfunctional structure. The presence of multiple hydroxyl groups enables extensive hydrogen bonding, which enhances its solubility in polar solvents. This property facilitates unique molecular interactions, allowing for effective stabilization of transition states during reactions. Furthermore, its chiral centers contribute to specific stereochemical outcomes, influencing reaction pathways and selectivity in various chemical processes. |