Jojoba Alcohol
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Jojoba Alcohol
Jojoba alcohol is the alcohol fraction obtained by the saponification of jojoba oil from the seeds of ''Simmondsia chinensis''. Jojoba alcohol is commonly used in cosmetic formulations. Chemical constituents Jojoba alcohol is a mixture of both saturated and unsaturated long chain alcohols of between 16 and 26 carbons in chain length, including: *C16:0 Hexadecanol *C17:1 ''cis''-8-Heptadecenol *C18:0 Octadecanol *C18:1 ''cis''-9-Octadecenol *C18:1 ''cis''-11-Octadecenol *C20:0 Eicosanol *C20:1 ''cis''-11-Eicosenol *C21:1 ''cis''-12-Heneicosenol *C22:0 Docosanol 1-Docosanol, also known as behenyl alcohol, is a saturated fatty alcohol containing 22 carbon atoms, used traditionally as an emollient, emulsifier, and thickener in cosmetics. In July 2000, docosanol was approved for medical use in the Unite ... *C22:1 ''cis''-13-Docosenol *C24:1 ''cis''-15-Tetracosenol *C26:0 Hexacosanol Physical properties Jojoba alcohol is a clear, colorless liquid at room tempera ...
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Alcohol (chemistry)
In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl () functional group bound to a saturated carbon atom. The term ''alcohol'' originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula . Simple monoalcohols that are the subject of this article include primary (), secondary () and tertiary () alcohols. The suffix ''-ol'' appears in the IUPAC chemical name of all substances where the hydroxyl group is the functional group with the highest priority. When a higher priority group is present in the compound, the prefix ''hydroxy-'' is used in its IUPAC name. The suffix ''-ol'' in non-IUPAC names (such as paracetamol or cholesterol) also typically indicates that the substance is an alcohol. However, some compou ...
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Jojoba Wax Esters
Jojoba wax esters are polyethylene glycol derivatives of the acids and alcohols obtained from the saponification of jojoba oil. With an average ethoxylation value of 80, it is known as jojoba wax PEG-80 esters or PEG-80 jojoba. With an average ethoxylation value of 120, it is known as jojoba wax PEG-120 esters or PEG-120 jojoba. Jojoba wax esters are used in cosmetic formulations as emollient A moisturizer, or emollient, is a cosmetic preparation used for protecting, moisturizing, and lubricating the skin. These functions are normally performed by sebum produced by healthy skin. The word "emollient" is derived from the Latin verb ''m ...s. References Cosmetics chemicals {{ester-stub ...
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Jojoba Ester
Jojoba esters are the hydrogenation or transesterification product of Jojoba oil. Jojoba Esters are commonly used in cosmetic formulations as an emollient, due to its remarkable similarity to the natural oils produced by the human skin, and its high oxidative stability. Fully hydrogenated jojoba esters are most often small beads used to exfoliate the skin. Chemical structure Jojoba esters are proper waxes; there is no triglyceride component of jojoba esters. Chemically, jojoba esters are a complex mixture of long chain fatty acids and fatty alcohols joined by an ester bond, resulting in a total length of 36 to 46 carbon atoms. Jojoba esters are produced by the interesterification of jojoba oil, hydrogenated jojoba oil, or a mixture of the two. Pure jojoba oil and pure hydrogenated jojoba oil are also correctly described as jojoba esters. The CTFA does not regard ''partially''-hydrogenated jojoba oil as jojoba esters. For this reason, jojoba esters must not contain any trans-un ...
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Docosanol
1-Docosanol, also known as behenyl alcohol, is a saturated fatty alcohol containing 22 carbon atoms, used traditionally as an emollient, emulsifier, and thickener in cosmetics. In July 2000, docosanol was approved for medical use in the United States as an antiviral agent for reducing the duration of cold sores. It is an over-the-counter medication (OTC). It is sold under the brand name Abreva among others. Side effects One of the most common side effects that has been reported from docosanol is headache. Headaches caused by the medication tend to be mild and can occur in any region of the head. In clinical trials, headache occurred in 10.4% of people treated with docosanol cream and 10.7% of people treated with placebo. The most serious side effects, although rare, are allergic reactions. Some of the patients experienced the symptoms of allergic reactions, including difficulty breathing, confusion, angioedema (facial swelling), fainting, dizziness, hives or chest pain. ...
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Eicosanol
Arachidyl alcohol, also 1-icosanol, is a waxy substance used as an emollient in cosmetics. It is a straight-chain fatty alcohol with 20 carbon atoms, typically obtained via the hydrogenation of arachidic acid or arachidonic acid, both of which are present in peanut oil. Its name is derived from that of the peanut The peanut (''Arachis hypogaea''), also known as the groundnut, goober (US), pindar (US) or monkey nut (UK), is a legume crop grown mainly for its edible Seed, seeds. It is widely grown in the tropics and subtropics, important to both small ... plant (Latin: ''arachis''). References {{Alcohols Fatty alcohols Primary alcohols Alkanols ...
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Saponification
Saponification is a process of converting esters into soaps and alcohols by the action of aqueous alkali (for example, aqueous sodium hydroxide solutions). Soaps are salts of fatty acids, which in turn are carboxylic acids with long carbon chains. Sodium stearate is a typical soap. Saponification of fats Vegetable oils and animal fats are the traditional materials that are saponified. These greasy materials, triesters called triglycerides, are mixtures derived from diverse fatty acids. Triglycerides can be converted to soap in either a one- or a two-step process. In the traditional one-step process, the triglyceride is treated with a strong base (e.g. lye), which cleaves the ester bond, releasing fatty acid salts (soaps) and glycerol. This process is also the main industrial method for producing glycerol. In some soap-making, the glycerol is left in the soap. If necessary, soaps may be precipitated by salting it out with sodium chloride. Fat in a corpse converts into adipoce ...
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