Solubilization of terpin hydrate and anethole was written by Regdon-Kiss, E.;Mester, L.. And the article was included in Pharmazie in 1966.Formula: C10H22O3 This article mentions the following:
Earlier studies (CA 60, 9104c) were continued in an effort to demonstrate surface tension changes during, and to explain the mechanism of, solubilization of insoluble substances. Maximum solubilization of 0.3% terpin hydrate (I) occurred with 5% Tweens; the solution was stable for ≥2 months when Tween 20 was used. Thus, a large excess, ten times or more, of solubilizing agent must be used. I itself possesses a small degree of surface activity, a 1% concentration reducing the surface-tension of aqueous Tween solutions to a small extent. I incorporated in the micellae plays a role at the surface of the solution, but the filmlike wedged-in association of the combined Tweens-H2O-I is also involved. Anethole (II) and anise oil aqueous suspensions behave like I as regards the surface tension of Tweens. Both reduce the surface tension of Tween 20 solution to approx. the same extent. The greatest reduction was with 0.01% Tween 20. Just as with I, here also it was shown that surface tension changes resulted from filmlike association of Tweens-H2O-II (or anise oil). In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Formula: C10H22O3).
rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Formula: C10H22O3
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts