An essential oil is a concentrated hydrophobic liquid containing volatile (easily evaporated at normal temperatures) chemical compounds from plants. Essential oils are also known as volatile oils, ethereal oils, aetherolea, or simply as the oil of the plant from which they were extracted, such as oil of clove. An essential oil is "essential" in the sense that it contains the "essence of" the plant's fragrance--the characteristic fragrance of the plant from which it is derived. The term "essential" used here does not mean indispensable, as with the terms essential amino acid or essential fatty acid, which are so called because they are nutritionally required by a given living organism. In contrast to fatty oils, essential oils typically evaporate completely without leaving a stain or residue.
Essential oils are generally extracted by distillation, often by using steam. Other processes include expression, solvent extraction, sfumatura, absolute oil extraction, resin tapping, wax embedding, and cold pressing. They are used in perfumes, cosmetics, soaps and other products, for flavoring food and drink, and for adding scents to incense and household cleaning products.
Essential oils are often used for aromatherapy, a form of alternative medicine in which healing effects are ascribed to aromatic compounds. Aromatherapy may be useful to induce relaxation, but there is not sufficient evidence that essential oils can effectively treat any condition. Improper use of essential oils may cause harm including allergic reactions and skin irritation, and children may be particularly susceptible to the toxic effects of improper use.
Essential oils have been used in folk medicine throughout history. The earliest recorded mention of the techniques and methods used to produce essential oils is believed to be that of Ibn al-Baitar (1188-1248), an Al-Andalusian (Muslim Spain) physician, pharmacist and chemist.
Rather than refer to essential oils themselves, modern works typically discuss specific chemical compounds which the essential oils are composed of, such as referring to methyl salicylate rather than "oil of wintergreen".
Interest in essential oils has revived in recent decades with the popularity of aromatherapy, a branch of alternative medicine that uses essential oils and other aromatic compounds. Oils are volatilized, diluted in a carrier oil and used in massage, diffused in the air by a nebulizer, heated over a candle flame, or burned as incense.
Medical applications proposed by those who sell medicinal oils range from skin treatments to remedies for cancer and often are based solely on historical accounts of use of essential oils for these purposes. Claims for the efficacy of medical treatments, and treatment of cancers in particular, are now subject to regulation in most countries.
Most common essential oils such as lavender, peppermint, tea tree oil, patchouli, and eucalyptus are distilled. Raw plant material, consisting of the flowers, leaves, wood, bark, roots, seeds, or peel, is put into an alembic (distillation apparatus) over water. As the water is heated, the steam passes through the plant material, vaporizing the volatile compounds. The vapors flow through a coil, where they condense back to liquid, which is then collected in the receiving vessel.
The recondensed water is referred to as a hydrosol, hydrolat, herbal distillate, or plant water essence, which may be sold as another fragrant product. Hydrosols include rose water, lavender water, lemon balm, clary sage, and orange blossom water. The use of herbal distillates in cosmetics is increasing.
Most citrus peel oils are expressed mechanically or cold-pressed (similar to olive oil extraction). Due to the relatively large quantities of oil in citrus peel and low cost to grow and harvest the raw materials, citrus-fruit oils are cheaper than most other essential oils. Lemon or sweet orange oils are obtained as byproducts of the citrus industry.
Before the discovery of distillation, all essential oils were extracted by pressing.
Most flowers contain too little volatile oil to undergo expression, but their chemical components are too delicate and easily denatured by the high heat used in steam distillation. Instead, a solvent such as hexane or supercritical carbon dioxide is used to extract the oils. Extracts from hexane and other hydrophobic solvents are called concretes, which are a mixture of essential oil, waxes, resins, and other lipophilic (oil-soluble) plant material.
Although highly fragrant, concretes contain large quantities of non-fragrant waxes and resins. Often, another solvent, such as ethyl alcohol, is used to extract the fragrant oil from the concrete. The alcohol solution is chilled to -18 °C (0 °F) for more than 48 hours which causes the waxes and lipids to precipitate out. The precipitates are then filtered out and the ethanol is removed from the remaining solution by evaporation, vacuum purge, or both, leaving behind the absolute.
Supercritical carbon dioxide is used as a solvent in supercritical fluid extraction. This method can avoid petrochemical residues in the product and the loss of some "top notes" when steam distillation is used. It does not yield an absolute directly. The supercritical carbon dioxide will extract both the waxes and the essential oils that make up the concrete. Subsequent processing with liquid carbon dioxide, achieved in the same extractor by merely lowering the extraction temperature, will separate the waxes from the essential oils. This lower temperature process prevents the decomposition and denaturing of compounds. When the extraction is complete, the pressure is reduced to ambient and the carbon dioxide reverts to a gas, leaving no residue.
Florasol is another solvent used to obtain essential oils. It was originally developed as a refrigerant to replace Freon. Although Florasol is an "ozone-friendly" product, it has a high global warming potential (GWP; 100-yr GWP = 1430). The European Union has banned its use, with a phase-out process that began in 2011, to be completed in 2017. One advantage of Florasol is that the extraction of essential oils occurs at or below room temperature so degradation through high temperature extremes does not occur. The essential oils are mostly pure and contain little to no foreign substances.
Estimates of total production of essential oils are difficult to obtain. One estimate, compiled from data in 1989, 1990, and 1994 from various sources, gives the following total production, in tonnes, of essential oils for which more than 1,000 tonnes were produced.
Taken by mouth, many essential oils can be dangerous in high concentrations. Typical effects begin with a burning feeling, followed by salivation. Different essential oils may have drastically different pharmacology. Some act as local anesthetic counterirritants and, thereby, exert an antitussive effect. Many essential oils, particularly tea tree oil, may cause contact dermatitis. Menthol and some others produce a feeling of cold followed by a sense of burning.
Aromatherapy is a form of alternative medicine in which healing effects are ascribed to the aromatic compounds in essential oils and other plant extracts. Aromatherapy may be useful to induce relaxation, but there is not sufficient evidence that essential oils can effectively treat any condition. Scientific research indicates that essential oils cannot treat or cure any chronic disease or other illnesses. Much of the research on the use of essential oils for health purposes has serious methodological errors. In a systemic review of 201 published studies on essential oils as alternative medicines, only 10 were found to be of acceptable methodological quality, and even these 10 were still weak in reference to scientific standards. Use of essential oils may cause harm including allergic reactions and skin irritation; there has been at least one case of death. As such, the use of essential oils as an alternative medicine should be approached with caution.
Research has shown that essential oils have potential as a natural pesticide. In case studies, certain oils have been shown to have a variety of deterring effects on pests, specifically insects and select arthropods. These effects may include repelling, inhibiting digestion, stunting growth, decreasing rate of reproduction, or death of pests that consume the oil. However, the molecules within the oils that cause these effects are normally non-toxic for mammals. These specific actions of the molecules allow for widespread use of these green pesticides without harmful effects to anything other than pests. Essential oils that have been investigated include rose, lemon grass, lavender, thyme, peppermint, and eucalyptus.
Although they may not be the perfect replacement for all synthetic pesticides, essential oils have prospects for crop or indoor plant protection, urban pest control, and marketed insect repellants, such as bug spray. Certain essential oils have been shown in studies to be comparable, if not exceeding, in effectiveness to DEET, which is currently marketed as the most effective mosquito repellent. Although essential oils are effective as pesticides when first applied in uses such as mosquito repellent applied to the skin, it is only effective in the vapor stage. Since this stage is relatively short-lived, creams and polymer mixtures are used in order to elongate the vapor period of effective repellency.
In any form, using essential oils as green pesticides rather than synthetic pesticides has ecological benefits such as decreased residual actions. In addition, increased use of essential oils as pest control could have not only ecological, but economical benefits as the essential oil market diversifies and popularity increases among organic farmers and environmentally conscious consumers.
In relation with their food applications, although these oils have been used throughout history as food preservatives, it was in the 20th century when EOs were considered as Generally Recognized as Safe (GRAS) by the Food and Drug Administration (FDA).
|Common Name||Botanical Name of Plant Source|
|Alfalfa||Medicago sativa L.|
|Allspice||Pimenta officinalis Lindl.|
|Almont, bitter (pure from prussic acid)||Prunnus amygdalus Batsch, Prussun armeniaca L., or Prunnus persica (L.) Batsch.|
|Ambrette (seed)||Hibiscus moschatus Moench.|
|Angelica root||Angelica archangelica L.|
|Angostura (cusparia bark)||Galipea officinalis Hancock.|
|Anise||Pimpinella anisum L.|
|Asafetida||Ferula assa-foetida L. and related spp. of Ferula.|
|Balm (lemon balm)||Melissa officinalis L.|
|Balsam of Peru||Myroxylon pereirae Klotzsch.|
|Basil||Ocimum basilicum L.|
|Bay leaves||Laurus nobilis L.|
|Bay (myrcia oil)||Pimenta racemosa (Mill.) J. W. Moore.|
|Bergamot (bergamot orange)||Citrus aurantium L. subsp. bergamia Wright et Arn.|
|Bitter almond (free from prussic acid)||Prunus amygdalus Batsch, Prunus armeniaca L., or Prunus persica (L.) Batsch.|
|Bois de rose||Aniba rosaeodora Ducke.|
|Cacao||Theobroma cacao L.|
|Camomile (chamomile) flowers, Hungarian||Matricaria chamomilla L.|
|Camomile (chamomile) flowers, Roman or English||Anthemis nobilis L.|
|Cananga||Cananga odorata Hook. f. and Thoms.|
|Capsicum||Capsicum frutescens L. and Capsicum annuum L.|
|Caraway||Carum carvi L.|
|Cardamom seed (cardamon)||Elettaria cardamomum Maton.|
|Carob bean||Ceratonia siliqua L.|
|Carrot||Daucus carota L.|
|Cascarilla bark||Croton eluteria Benn.|
|Cassia bark, Chinese||Cinnamomum cassia Blume.|
|Cassia bark, Padang or Batavia||Cinnamomum burmanni Blume.|
|Cassia bark, Saigon||Cinnamomum loureirii Nees.|
|Celery seed||Apium graveolens L.|
|Cherry, wild, bark||Prunus serotina Ehrh.|
|Chervil||Anthriscus cerefolium (L.) Hoffm.|
|Chicory||Cichorium intybus L.|
|Cinnamon bark, Ceylon||Cinnamomum zeylanicum Nees.|
|Cinnamon bark, Chinese||Cinnamomum cassia Blume.|
|Cinnamon bark, Saigon||Cinnamomum loureirii Nees.|
|Cinnamon leaf, Ceylon||Cinnamomum zeylanicum Nees.|
|Cinnamon leaf, Chinese||Cinnamomum cassia Blume.|
|Cinnamon leaf, Saigon||Cinnamomum loureirii Nees.|
|Citronella||Cymbopogon nardus Rendle.|
|Citrus peels||Citrus spp.|
|Clary (clary sage)||Salvia sclarea L.|
|Coca (decocainized)||Erythroxylum coca Lam. and other spp. of Erythroxylum.|
|Cola nut||Cola acuminata Schott and Endl., and other spp. of Cola.|
|Coriander||Coriandrum sativum L.|
|Cumin (cummin)||Cuminum cyminum L.|
|Curacao orange peel (orange, bitter peel)||Citrus aurantium L.|
|Cusparia bark||Galipea officinalis Hancock.|
|Dandelion||Taraxacum officinale Weber and T. laevigatum DC.|
|Dog grass (quackgrass, triticum)||Agropyron repens (L.) Beauv.|
|Elder flowers||Sambucus canadensis L. and S. nigra I.|
|Estragole (esdragol, esdragon, tarragon)||Artemisia dracunculus L.|
|Fennel, sweet||Foeniculum vulgare Mill.|
|Fenugreek||Trigonella foenum-graecum L.|
|Galanga (galangal)||Alpinia officinarum Hance.|
|Geranium, East Indian||Cymbopogon martini Stapf.|
|Geranium, rose||Pelargonium graveolens L'Her.|
|Ginger||Zingiber officinale Rosc.|
|Grapefruit||Citrus paradisi Macf.|
|Hickory bark||Carya spp.|
|Horehound (hoarhound)||Marrubium vulgare L.|
|Hops||Humulus lupulus L.|
|Horsemint||Monarda punctata L.|
|Hyssop||Hyssopus officinalis L.|
|Immortelle||Helichrysum augustifolium DC.|
|Jasmine||Jasminum officinale L. and other spp. of Jasminum.|
|Juniper (berries)||Juniperus communis L.|
|Kola nut||Cola acuminata Schott and Endl., and other spp. of Cola.|
|Laurel berries||Laurus nobilis L.|
|Laurel leaves||Laurus spp.|
|Lavender||Lavandula officinalis Chaix.|
|Lavender, spike||Lavandula latifolia Vill.|
|Lavandin||Hybrids between Lavandula officinalis Chaix and Lavandula latifolin Vill.|
|Lemon||Citrus limon (L.) Burm. f.|
|Lemon balm (see balm)|
|Lemon grass||Cymbopogon citratus DC. and Cymbopogon lexuosus Stapf.|
|Lemon peel||Citrus limon (L.) Burm. f.|
|Lime||Citrus aurantifolia Swingle.|
|Linden flowers||Tilia spp.|
|Locust bean||Ceratonia siliqua L,|
|Lupulin||Humulus lupulus L.|
|Mace||Myristica fragrans Houtt.|
|Mandarin||Citrus reticulata Blanco.|
|Marjoram, sweet||Majorana hortensis Moench.|
|Mate||Ilex paraguariensis St. Hil.|
|Melissa (see balm)|
|Molasses (extract)||Saccarum officinarum L.|
|Naringin||Citrus paradisi Macf.|
|Neroli, bigarade||Citrus aurantium L.|
|Nutmeg||Myristica fragrans Houtt.|
|Onion||Allium cepa L.|
|Orange, bitter, flowers||Citrus aurantium L.|
|Orange, bitter, peel||Do.|
|Orange leaf||Citrus sinensis (L.) Osbeck.|
|Orange, sweet, flowers||Do.|
|Orange, sweet, peel||Do.|
|Palmarosa||Cymbopogon martini Stapf.|
|Paprika||Capsicum annuum L.|
|Parsley||Petroselinum crispum (Mill.) Mansf.|
|Pepper, black||Piper nigrum L.|
|Peppermint||Mentha piperita L.|
|Peruvian balsam||Myroxylon pereirae Klotzsch.|
|Petitgrain||Citrus aurantium L.|
|Petitgrain lemon||Citrus limon (L.) Burm. f.|
|Petitgrain mandarin or tangerine||Citrus reticulata Blanco.|
|Pimenta||Pimenta officinalis Lindl.|
|Pimenta leaf||Pimenta officinalis Lindl.|
|Pipsissewa leaves||Chimaphila umbellata Nutt.|
|Pomegranate||Punica granatum L.|
|Prickly ash bark||Xanthoxylum (or Zanthoxylum) Americanum Mill. or Xanthoxylum clava-herculis L.|
|Rose absolute||Rosa alba L., Rosa centifolia L., Rosa damascena Mill., Rosa gallica L., and vars. of these spp.|
|Rose (otto of roses, attar of roses)||Do.|
|Rose fruit (hips)||Do.|
|Rose geranium||Pelargonium graveolens L'Her.|
|Rose leaves||Rosa spp.|
|Rosemary||Rosmarinus officinalis L.|
|Saffron||Crocus sativus L.|
|Sage||Salvia officinalis L.|
|Sage, Greek||Salvia triloba L.|
|Sage, Spanish||Salvia lavandulaefolia Vahl.|
|St. John's bread||Ceratonia siliqua L.|
|Savory, summer||Satureia hortensis L.|
|Savory, winter||Satureia montana L.|
|Schinus molle||Schinus molle L.|
|Sloe berries (blackthorn berries)||Prunus spinosa L.|
|Spearmint||Mentha spicata L.|
|Spike lavender||Lavandula latifolia Vill.|
|Tamarind||Tamarindus indica L.|
|Tangerine||Citrus reticulata Blanco.|
|Tarragon||Artemisia dracunculus L.|
|Tea||Thea sinensis L.|
|Thyme||Thymus vulgaris L. and Thymus zygis var. gracilis Boiss.|
|Thyme, wild or creeping||Thymus serpyllum L.|
|Triticum (see dog grass)|
|Tuberose||Polianthes tuberosa L.|
|Turmeric||Curcuma longa L.|
|Vanilla||Vanilla planifolia Andr. or Vanilla tahitensis J. W. Moore.|
|Violet flowers||Viola odorata L.|
|Violet leaves absolute||Do.|
|Wild cherry bark||Prunus serotina Ehrh.|
|Ylang-ylang||Cananga odorata Hook. f. and Thoms.|
|Zedoary bark||Curcuma zedoaria Rosc.|
Essential oils are usually lipophilic (literally: "oil-loving") compounds that usually are not miscible with water. They can be diluted in solvents like pure ethanol and polyethylene glycol. The most common way to safely dilute essential oils for topical use is in a carrier oil. This can be any vegetable oil readily available, the most popular for skin care being jojoba, coconut, wheat germ, olive and avocado.
Essential oils are derived from sections of plants. Some plants, like the bitter orange, are sources of several types of essential oil.
Balsam of Peru, an essential oil derived from the Myroxylon, is used in food and drink for flavoring, in perfumes and toiletries for fragrance, and in medicine and pharmaceutical items for healing properties. However, a number of national and international surveys have identified Balsam of Peru as being in the "top five" allergens most commonly causing patch test allergic reactions in people referred to dermatology clinics.
Most eucalyptus oil on the market is produced from the leaves of Eucalyptus globulus. Steam-distilled eucalyptus oil is used throughout Asia, Africa, Latin America and South America as a primary cleaning/disinfecting agent added to soaped mop and countertop cleaning solutions; it also possesses insect and limited vermin control properties. Note, however, there are hundreds of species of eucalyptus, and perhaps some dozens are used to various extents as sources of essential oils. Not only do the products of different species differ greatly in characteristics and effects, but also the products of the very same tree can vary grossly.
Lavender oil has long been used in the production of perfume. However, it can be estrogenic and antiandrogenic, causing problems for prepubescent boys and pregnant women, in particular. Lavender essential oil is also used as an insect repellent.
The potential danger of an essential oil is sometimes relative to its level or grade of purity, and sometimes related to the toxicity of specific chemical components of the oil. Many essential oils are designed exclusively for their aroma-therapeutic quality; these essential oils generally should not be applied directly to the skin in their undiluted or "neat" form. Some can cause severe irritation, provoke an allergic reaction and, over time, prove hepatotoxic.
Industrial users of essential oils should consult the safety data sheets (SDS) to determine the hazards and handling requirements of particular oils. Even certain therapeutic grade oils can pose potential threats to individuals with epilepsy or pregnant women.
Essential oil use in children can pose a danger when misused because of their thin skin and immature livers. This might cause them to be more susceptible to toxic effects than adults. 
The flash point of each essential oil is different. Many of the common essential oils, such as tea tree, lavender, and citrus oils, are classed as a Class 3 Flammable Liquid, as they have a flash point of 50-60 °C.
Estrogenic and antiandrogenic activity have been reported by in vitro study of tea tree oil and lavender essential oils. Two published sets of case reports suggest the lavender oil may be implicated in some cases of gynecomastia, an abnormal breast tissue growth in prepubescent boys. The European Commission's Scientific Committee on Consumer Safety dismissed the claims against tea tree oil as implausible, but did not comment on lavender oil. In 2018, a BBC report on a study stated that tea tree and lavender oils contain eight substances that when tested in tissue culture experiments, increasing the level of estrogen and decreasing the level of testosterone. Some of the substances are found in "at least 65 other essential oils". The study did not include animal or human testing.
Exposure to essential oils may cause a contact dermatitis. Essential oils can be aggressive toward rubbers and plastics, so care must be taken in choosing the correct handling equipment. Glass syringes are often used, but have coarse volumetric graduations. Chemistry syringes are ideal, as they resist essential oils, are long enough to enter deep vessels, and have fine graduations, facilitating quality control. Unlike traditional pipettes, which have difficulty handling viscous fluids, the chemistry syringe, also known as a positive displacement pipette, has a seal and piston arrangement which slides inside the pipette, wiping the essential oil off the pipette wall.
Some essential oils qualify as GRAS flavoring agents for use in foods, beverages, and confectioneries according to strict Good Manufacturing Practice (GMP) and flavorist standards.Pharmacopoeia standards for medicinal oils should be heeded. Some oils can be toxic to some domestic animals, cats in particular. The internal use of essential oils can pose hazards to pregnant women, as some can be abortifacients in dose 0.5-10 mL, and thus should not be used during pregnancy.
There is some concern about pesticide residues in essential oils, particularly those used therapeutically. For this reason, many practitioners of aromatherapy buy organically produced oils. Not only are pesticides present in trace quantities, but also the oils themselves are used in tiny quantities and usually in high dilutions. Where there is a concern about pesticide residues in food essential oils, such as mint or orange oils, the proper criterion is not solely whether the material is organically produced, but whether it meets the government standards based on actual analysis of its pesticide content.
Certain essential oils are safe to use during pregnancy, but care must be taken when selecting quality and brand. Some essential oils may contain impurities and additives that may be harmful to pregnant women. Sensitivity to certain smells may cause pregnant women to have adverse side effects with essential oil use, such as headache, vertigo, and nausea. Pregnant women often report an abnormal sensitivity to smells and taste, and essential oils can cause irritation and nausea when ingested. Always consult a doctor before use.
The following table lists the LD50 or median lethal dose for common oils; this is the dose required to kill half the members of a tested animal population. LD50 is intended as a guideline only, and reported values can vary widely due to differences in tested species and testing conditions.
|Common Name||Oral LD50||Dermal LD50||Notes|
|Neem||14 g/kg||>2 g/kg|
|Lemon myrtle||2.43 g/kg||2.25 g/kg|
|Frankincense||>5 g/kg||>5 g/kg||Boswellia carterii|
|Frankincense||>2 g/kg||>2 g/kg||Boswellia sacra|
|Indian frankincense||>2 g/kg||>2 g/kg||Boswellia serrata|
|Ylang-ylang||>5 g/kg||>5 g/kg|
|Cedarwood||>5 g/kg||>5 g/kg|
|Roman chamomile||>5 g/kg||>5 g/kg|
|White camphor||>5 g/kg||>5 g/kg||Cinnamomum camphora, extracted from leaves|
|Yellow camphor||3.73 g/kg||>5 g/kg||Cinnamomum camphora, extracted from bark|
|Hot oil||3.80 g/kg||>5 g/kg||Cinnamomum camphora, oil extracted from leaves|
|Cassia||2.80 g/kg||0.32 g/kg|
In 2002, ISO published ISO 4720 in which the botanical names of the relevant plants are standardized. The rest of the standards with regards to this topic can be found in the section of ICS 71.100.60 
A suspected link between abnormal breast growth in young boys and the use of lavender and tea tree oils has been given new weight, after a study found eight chemicals contained in the oils interfere with hormones.