(+)-13-epi-Manool - Names and Identifiers
Name | 13-Epimanool
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Synonyms | 13-Epimanool epi-13-Manool (+)-13-epi-Manool 1-Naphthalenepropanol,.alp (13S)-Labda-8(17),14-dien-13-ol [13S,(+)]-Labda-8(17),14-dien-13-ol (1S,αS,4aα)-α-Ethenyldecahydro-α,5,5,8aβ-tetramethyl-2-methylene-1β-naphthalene-1-propanol 1-Naphthalenepropanol, α-ethenyldecahydro-α,5,5,8a-tetramethyl-2-methylene-, (αS,1S,4aS,8aS)-
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CAS | 1438-62-6
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(+)-13-epi-Manool - Physico-chemical Properties
Molecular Formula | C20H34O
|
Molar Mass | 290.49 |
Density | 0.93±0.1 g/cm3(Predicted) |
Melting Point | 35-38 °C |
Boling Point | 368.2±11.0 °C(Predicted) |
Specific Rotation(α) | +51 (c, 1.3 in CHCl3) |
pKa | 14.47±0.29(Predicted) |
Storage Condition | 2-8℃ |
(+)-13-epi-Manool - Introduction
13-Epimanool is an organic compound with the molecular formula C10H14O.
Nature:
13-Epimanool is a colorless liquid with aromatic flavor. It has a density of 0.971 g/mL, a boiling point of 180-182°C and a flash point of 75°C. The compounds are soluble in organic solvents such as alcohols and ethers at room temperature.
Use:
13-Epimanool is widely used in the fragrance and fragrance industry. It is often used as a perfuming agent, giving products such as perfumes, soaps, shampoos and skin care products an aromatic odor.
Method:
13-Epimanool synthesis method is mainly through chemical synthesis to complete. One commonly used method of preparation is to react geraniol with an acid catalyst such as sulfuric acid and the like to produce 13-Epimanool.
Safety Information:
There are relatively few studies on the toxicity and danger of 13-Epimanool, so it needs to be used with caution. When using 13-Epimanool should follow general chemical safety practices, such as wearing protective gloves and glasses, and operating in a well-ventilated area. If exposed or inhaled, wash the affected area immediately and seek medical help. When storing and handling 13-Epimanool, keep it away from ignition and flammable materials.
Last Update:2024-04-09 20:49:11