Isopulegol

CAS: 89-79-2

Ref. 3D-FI106423

Produktinformation

• Name: Isopulegol
• Synonyme: (-)-<span class="text-smallcaps">L</span>-Isopulegol, (1R,2S,5R)-(-)-Isopulegol, (1R,2S,5R)-2-Isopropenyl-5-methylcyclohexanol, (1R,2S,5R)-5-Methyl-2-(1-methylethenyl)cyclohexanol, (1R,2S,5R)-5-methyl-2-(prop-1-en-2-yl)cyclohexanol, 1-Methyl-4-isopropenylcyclohexan-3-ol, Coolact, Cyclohexanol, 5-methyl-2-(1-methylethenyl)-, (1R,2S,5R)-, Cyclohexanol, 5-methyl-2-(1-methylethenyl)-, [1R-(1α,2β,5α)]-, Isopugenol I, Isopulegol I, P-Menth-8-En-3-Ol, iso-Pulegol, l-Isopulegol, p-Menth-8-en-3-ol, (1R,3R,4S)-(-)-, trans-Isoperitenol
• CAS: 89-79-2

Beschreibung

Isopulegol is a nitro compound that has been identified as an endogenous depressant of ATP-sensitive K+ channels. Isopulegol is synthesized by the asymmetric synthesis of cyclohexanone and 1,1-dimethoxypropane with hydrochloric acid. The reaction mechanism involves the conversion of cyclohexanone to isopulegol in an intramolecular electrophilic substitution reaction. Isopulegol is most commonly found bound to proteins, but it can also exist in its free form. The binding affinity between isopulegol and ATP-sensitive K+ channels depends on the formation of a stable complex with a phenolic hydroxyl group and a carbonyl group that are necessary for the binding site.
Isopulegol has been shown to have analgesic effects in rats, which may be due to its ability to inhibit pain signals from reaching the brain by blocking nerve impulses at their origin

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 154.25 g/mol
• Formel: C₁₀H₁₈O
• Reinheit: Min. 95%
• Farbe/Form: Colorless Clear Liquid