N-[2-(3,4-Dihydroxyphenyl)ethyl]octadecanamide, with the CAS number 105955-10-0, is a chemical compound characterized by its long-chain fatty acid amide structure. This compound features an octadecanamide backbone, which consists of an 18-carbon saturated fatty acid chain, providing hydrophobic properties. The presence of the 3,4-dihydroxyphenyl group introduces polar characteristics due to the hydroxyl (-OH) functional groups, which can engage in hydrogen bonding and enhance solubility in polar solvents. This dual nature of the molecule contributes to its potential applications in various fields, including pharmaceuticals and cosmetics, where both hydrophobic and hydrophilic interactions are beneficial. The compound may exhibit biological activity, possibly influencing cellular processes or serving as a surfactant. Its stability and reactivity can be influenced by the presence of the hydroxyl groups, which may also participate in oxidation reactions. Overall, N-[2-(3,4-dihydroxyphenyl)ethyl]octadecanamide represents a unique blend of hydrophobic and hydrophilic characteristics, making it a subject of interest in chemical research and application.

N-[2-(3,4-DIHYDROXYPHENYL)ETHYL]OCTADECANAMIDE

105955-10-0: N-[2-(3,4-Dihydroxyphenyl)ethyl]octadecanamide, with the CAS number 105955-10-0, is a chemical compound characterized by its long-chain fatty acid amide structure. This compound features an octadecanamide backbone, which consists of an 18-carbon saturated fatty acid chain, providing hydrophobic properties. The presence of the 3,4-dihydroxyphenyl group introduces polar characteristics due to the hydroxyl (-OH) functional groups, which can engage in hydrogen bonding and enhance solubility in polar solvents. This dual nature of the molecule contributes to its potential applications in various fields, including pharmaceuticals and cosmetics, where both hydrophobic and hydrophilic interactions are beneficial. The compound may exhibit biological activity, possibly influencing cellular processes or serving as a surfactant. Its stability and reactivity can be influenced by the presence of the hydroxyl groups, which may also participate in oxidation reactions. Overall, N-[2-(3,4-dihydroxyphenyl)ethyl]octadecanamide represents a unique blend of hydrophobic and hydrophilic characteristics, making it a subject of interest in chemical research and application.

STEARDA potentiates TRPV1-mediated effects of NADA.

CAS 105955-10-0

N-[2-(3,4-DIHYDROXYPHENYL)ETHYL]OCTADECANAMIDE

STEARDA

Ref: TM-T23399