Amino Alcohols
Items 131 to 140 of 491 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-(N-Ethyl-N-m-toluidino)ethanol | 91-88-3 | sc-229866 | 25 g | $62.00 | ||
2-(N-Ethyl-N-m-toluidino)ethanol is an amino alcohol characterized by its unique ethyl and m-toluidine substituents, which enhance its steric and electronic properties. This compound exhibits strong hydrogen bonding capabilities due to its hydroxyl and amino groups, facilitating specific molecular interactions. Its structure allows for selective reactivity in condensation reactions and offers a pathway for the formation of stable intermediates, influencing reaction kinetics and product distribution. | ||||||
2-(N-Ethylanilino)ethanol | 92-50-2 | sc-223261 | 100 g | $64.00 | ||
2-(N-Ethylanilino)ethanol is an amino alcohol characterized by its ethyl-substituted aniline moiety, which enhances its hydrophobic interactions while maintaining significant hydrogen bonding capabilities. This compound exhibits unique reactivity patterns due to its ability to participate in both nucleophilic and electrophilic reactions, influenced by the electron-donating effects of the ethyl group. Its structural flexibility allows for diverse conformational states, impacting its interaction with various substrates and reaction pathways. | ||||||
2-Amino-1-butanol | 96-20-8 | sc-237898 | 100 ml | $40.00 | ||
2-Amino-1-butanol is an amino alcohol notable for its primary amine and hydroxyl functional groups, which facilitate strong hydrogen bonding and enhance solubility in polar solvents. Its unique structure allows for intramolecular interactions that can stabilize transition states during chemical reactions. This compound exhibits distinct reactivity, participating in both condensation and substitution reactions, influenced by its steric and electronic properties, which can modulate reaction kinetics and pathways. | ||||||
N-Butyldiethanolamine | 102-79-4 | sc-236029 | 500 ml | $51.00 | ||
N-Butyldiethanolamine is an amino alcohol characterized by its dual hydroxyl and amine functionalities, promoting extensive hydrogen bonding and enhancing its affinity for various substrates. This compound exhibits unique steric effects that influence its reactivity, allowing it to engage in diverse chemical pathways, including nucleophilic attacks and complexation with metal ions. Its ability to form stable adducts and participate in dynamic equilibria makes it a versatile player in various chemical environments. | ||||||
2-(Dibutylamino)ethanol | 102-81-8 | sc-229860 sc-229860A | 100 ml 500 ml | $30.00 $50.00 | 1 | |
2-(Dibutylamino)ethanol is an amino alcohol distinguished by its branched alkyl chains, which contribute to its hydrophobic character and influence solubility in organic solvents. The presence of both amine and hydroxyl groups facilitates strong intermolecular interactions, including hydrogen bonding and dipole-dipole interactions. This compound can act as a nucleophile, engaging in reactions with electrophiles, and its unique sterics can modulate reaction kinetics, making it a key participant in various synthetic pathways. | ||||||
4-Aminophenethyl alcohol | 104-10-9 | sc-254608 | 5 g | $45.00 | ||
4-Aminophenethyl alcohol is an amino alcohol characterized by its aromatic ring, which enhances its ability to engage in π-π stacking interactions and hydrogen bonding. The presence of both amino and hydroxyl functional groups allows for versatile reactivity, enabling it to participate in nucleophilic substitutions and condensation reactions. Its unique electronic properties can influence reaction rates and selectivity, making it a significant compound in various chemical transformations. | ||||||
2-Methoxyethylamine | 109-85-3 | sc-238122 | 25 ml | $42.00 | ||
2-Methoxyethylamine is an amino alcohol distinguished by its ether and amine functionalities, which enable unique dipole-dipole interactions and hydrogen bonding. This compound exhibits enhanced nucleophilicity due to the electron-donating methoxy group, promoting its role in various substitution reactions. Its ability to stabilize transition states can influence reaction kinetics, making it a key player in synthetic pathways. Additionally, its polar nature contributes to solubility in a range of solvents, facilitating diverse chemical applications. | ||||||
2-Benzylaminoethanol | 104-63-2 | sc-229954 | 100 g | $27.00 | ||
2-Benzylaminoethanol is an amino alcohol distinguished by its aliphatic and aromatic components, which facilitate unique steric and electronic interactions. The amino group can engage in strong hydrogen bonding, while the benzyl moiety enhances lipophilicity, influencing solubility and reactivity. This compound exhibits notable reactivity in electrophilic aromatic substitution and can act as a nucleophile in various organic reactions, showcasing its versatility in synthetic pathways. | ||||||
2-(Isopropylamino)ethanol | 109-56-8 | sc-229862 | 250 ml | $29.00 | ||
2-(Isopropylamino)ethanol is an amino alcohol characterized by its branched isopropyl group, which imparts steric hindrance and influences molecular interactions. The presence of the amino group allows for robust hydrogen bonding, enhancing solubility in polar solvents. This compound can participate in nucleophilic attacks, facilitating diverse reaction mechanisms. Its unique structure also affects its reactivity in condensation reactions, making it a versatile intermediate in organic synthesis. | ||||||
3-Phenyl-1-propanol | 122-97-4 | sc-226174 | 50 g | $30.00 | ||
3-Phenyl-1-propanol is an amino alcohol notable for its aromatic structure, which introduces unique steric and electronic effects that influence its reactivity. The presence of the phenyl group enhances π-π stacking interactions, potentially stabilizing transition states during chemical reactions. This compound exhibits strong hydrogen bonding due to its hydroxyl group, which can significantly affect solubility and reactivity in polar environments. Its chiral nature also allows for diverse stereochemical pathways in synthesis. | ||||||