|Preferred IUPAC name
Racemic: DL-Limonene; Dipentene
3D model (JSmol)
|Molar mass||g·mol−1 136.238|
|Appearance||colorless to pale-yellow liquid|
|Melting point||−74.35 °C (−101.83 °F; 198.80 K)|
|Boiling point||176 °C (349 °F; 449 K)|
|Solubility||Miscible with benzene, chloroform, ether, CS2, and oils
soluble in CCl4
Chiral rotation ([α]D)
Refractive index (nD)
Std enthalpy of
|−6.128 MJ mol−1|
|Main hazards||Skin sensitizer / Contact dermatitis – After aspiration, pulmonary oedema, pneumonitis, and death |
|GHS signal word||Danger|
|H226, H304, H315, H317, H400, H410|
|P210, P233, P240, P241, P242, P243, P261, P264, P272, P273, P280, P301+330+331, P302+352, P303+361+353, P304+340, P312, P333+313, P362, P370+378, P391, P403+233, P235, P405, P501|
|Flash point||50 °C (122 °F; 323 K)|
|237 °C (459 °F; 510 K)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Limonene is a colorless liquid aliphatic hydrocarbon classified as a cyclic monoterpene, and is the major component in the oil of citrus fruit peels. The D–isomer, occurring more commonly in nature as the fragrance of oranges, is a flavoring agent in food manufacturing. It is also used in chemical synthesis as a precursor to carvone and as a renewables-based solvent in cleaning products. The less common L–isomer is found in mint oils and has a piny, turpentine-like odor.
Limonene takes its name from the peel of the lemon. Limonene is a chiral molecule, and biological sources produce one enantiomer: the principal industrial source, citrus fruit, contains D-limonene ((+)-limonene), which is the (R)–enantiomer. Racemic limonene is known as dipentene. D-Limonene is obtained commercially from citrus fruits through two primary methods: centrifugal separation or steam distillation.
Limonene is a relatively stable monoterpene and can be distilled without decomposition, although at elevated temperatures it cracks to form isoprene. It oxidizes easily in moist air to produce carveol, carvone, and limonene oxide. With sulfur, it undergoes dehydrogenation to p–cymene.
Limonene occurs commonly as the D– or (R)-enantiomer, but racemizes to dipentene at 300 °C. When warmed with mineral acid, limonene isomerizes to the conjugated diene α-terpinene (which can also easily be converted to p-cymene). Evidence for this isomerization includes the formation of Diels–Alder adducts between α-terpinene adducts and maleic anhydride.
It is possible to effect reaction at one of the double bonds selectively. Anhydrous hydrogen chloride reacts preferentially at the disubstituted alkene, whereas epoxidation with mCPBA occurs at the trisubstituted alkene.
In nature, limonene is formed from geranyl pyrophosphate, via cyclization of a neryl carbocation or its equivalent as shown. The final step involves loss of a proton from the cation to form the alkene.
The most widely practiced conversion of limonene is to carvone. The three-step reaction begins with the regioselective addition of nitrosyl chloride across the trisubstituted double bond. This species is then converted to the oxime with a base, and the hydroxylamine is removed to give the ketone-containing carvone.
Safety and research
D-Limonene applied to skin may cause irritation from contact dermatitis, but otherwise appears to be safe for human uses. Limonene is flammable as a liquid or vapor, and is toxic to aquatic life. There is no evidence for efficacy or regulatory approval of perillyl alcohol – the precursor for D-limonene – as a chemotherapeutic agent.
Limonene is common as a dietary supplement and as a fragrance ingredient for cosmetics products. As the main fragrance of citrus peels, D-limonene is used in food manufacturing and some medicines, such as a flavoring to mask the bitter taste of alkaloids, and as a fragrance in perfumery, aftershave lotions, bath products, and other personal care products. D-Limonene is also used as botanical insecticide. D-Limonene is used in the organic herbicide “Avenger”. It is added to cleaning products, such as hand cleansers to give a lemon or orange fragrance (see orange oil) and for its ability to dissolve oils. In contrast, L-limonene has a piny, turpentine-like odor.
Limonene is used as a solvent for cleaning purposes, such as the removal of oil from machine parts, as it is produced from a renewable source (citrus oil, as a byproduct of orange juice manufacture). It is used as a paint stripper and is also useful as a fragrant alternative to turpentine. Limonene is also used as a solvent in some model airplane glues and as a constituent in some paints. Commercial air fresheners, with air propellants, containing limonene are used by philatelists to remove self-adhesive postage stamps from envelope paper.
Limonene is also used as a solvent for filament-fused 3D printing. Printers can print the plastic of choice for the model, but erect supports and binders from HIPS, a polystyrene plastic that is easily soluble in limonene. As it is combustible, limonene has also been considered as a biofuel.
In preparing tissues for histology or histopathology, D-limonene is often used as a less toxic substitute for xylene when clearing dehydrated specimens. Clearing agents are liquids miscible with alcohols (such as ethanol or isopropanol) and with melted paraffin wax, in which specimens are embedded to facilitate cutting of thin sections for microscopy. In traditional medicine, D-limonene is marketed to relieve gallstones, gastroesophageal reflux disease, and heartburn, although none of these supposed effects is confirmed by high-quality clinical research.
- Perfume allergy
- Black pepper
- Vitex agnus-castus
- GHS Classification on [PubChem]
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- EPA Fact Sheet on Limonene, September 1994
- Avenger Material Safety Data Sheet http://nebula.wsimg.com/07de45c0af774ba73e06362ad1a56f06?AccessKeyId=C67FD801C8FC93742D64&disposition=0&alloworigin=1
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- Cyclone Power to Showcase External Combustion Engine at SAE Event, Green Car Congress, 20 September 2007
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- Mass spectrum of limonene
- Description of D-limonene on the International Chemical Safety Cards
- D-Limonene information from the United States Environmental Protection Agency