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IUPAC names
  • (unspecified): 1330-16-1 checkY
  • (1R-α): 7785-70-8 checkY
  • (1S-α): 7785-26-4 checkY
  • ((±)-α): 80-56-8 checkY
  • (β): 18172-67-3 checkY
3D model (JSmol)
ECHA InfoCard 100.029.170 Edit this at Wikidata
EC Number
  • (1R-α): 232-087-8
  • (unspecified): CC1=CCC2CC1C2(C)C
Molar mass 136.24 g/mol
Appearance Liquid
Density 0,86 g·cm−3 (alpha, 15 °C)[1][2]
Melting point −62 to −55 °C (−80 to −67 °F; 211 to 218 K) (alpha)[1]
Boiling point 155 to 156 °C (311 to 313 °F; 428 to 429 K) (alpha)[1]
Practically insoluble in water
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Pinene (C10H16) is a bicyclic monoterpene chemical compound.[1] There are two structural isomers of pinene found in nature: α-pinene and β-pinene. As the name suggests, both forms are important constituents of pine resin; they are also found in the resins of many other conifers, as well as in non-coniferous plants such as camphorweed (Heterotheca)[3] and big sagebrush (Artemisia tridentata). Both isomers are used by many insects in their chemical communication system. The two isomers of pinene constitute the major component of turpentine.


skeletal formula (1R)-(+)-alpha-pinene-2D-skeletal.png (1S)-(-)-alpha-pinene-2D-skeletal.png (1R)-(+)-beta-pinene-2D-skeletal.png (1S)-(-)-beta-pinene-2D-skeletal.png
perspective view X (1S)-(-)-alpha-pinene-2D-projected-skeletal.png X (1S)-(-)-beta-pinene-2D-projected-skeletal.png
ball-and-stick model X (1S)-(−)-alpha-pinene-from-xtal-3D-balls.png X (1S)-(−)-beta-pinene-from-xtal-3D-balls.png
name (1R)-(+)-α-pinene (1S)-(−)-α-pinene (1R)-(+)-β-pinene (1S)-(−)-β-pinene
CAS number 7785-70-8 7785-26-4 19902-08-0 18172-67-3


α-Pinene and β-pinene are both produced from geranyl pyrophosphate, via cyclisation of linaloyl pyrophosphate followed by loss of a proton from the carbocation equivalent. Researchers at the Georgia Institute of Technology and the Joint BioEnergy Institute have been able to synthetically produce pinene with a bacterium.[4]

Biosynthesis of pinene from geranyl pyrophosphate


Alpha-pinene is the most widely encountered terpenoid in nature[5] and is highly repellant to insects.[6]

Alpha-pinene appears in conifers and numerous other plants.[7] Pinene is a major component of the essential oils of Sideritis spp. (ironwort)[8] and Salvia spp. (sage).[9] Cannabis also contains alpha-pinene[7] and beta-pinene.[10] Resin from Pistacia terebinthus (commonly known as terebinth or turpentine tree) is rich in pinene. Pine nuts produced by pine trees contain pinene.[7]

Makrut lime fruit peel contains an essential oil comparable to lime fruit peel oil; its main components are limonene and β-pinene.[11]

The racemic mixture of the two forms of pinene is found in some oils like eucalyptus oil.[12]


In chemical industry, selective oxidation of pinene with some catalysts gives many compounds for perfumery, such as artificial odorants. An important oxidation product is verbenone, along with pinene oxide, verbenol, and verbenyl hydroperoxide.[13]

Pinene left verbenone right

Pinenes are the primary constituents of turpentine.

The use of pinene as a biofuel in spark ignition engines has been explored.[14] Pinene dimers have been shown to have heating values comparable to the jet fuel JP-10.[4]


  1. ^ a b c Record of alpha-Pinen in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 07-January-2016.
  2. ^ Record of beta-Pinen in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 07-January-2016.
  3. ^ Lincoln DE, Lawrence BM (1984). "The volatile constituents of camphorweed, heterotheca subaxillaris". Phytochemistry. 23 (4): 933–934. doi:10.1016/S0031-9422(00)85073-6.
  4. ^ a b Sarria S, Wong B, Martín HG, Keasling JD, Peralta-Yahya P (2014). "Microbial Synthesis of Pinene". ACS Synthetic Biology. 3 (7): 466–475. doi:10.1021/sb4001382. PMID access
  5. ^ Noma Y, Asakawa Y (2010). "Biotransformation of Monoterpenoids by Microorganisms, Insects, and Mammals". In Baser KH, Buchbauer G (eds.). Handbook of Essential Oils: Science, Technology, and Applications (2nd ed.). Boca Raton, FL: CRC Press. pp. 585–736. ISBN 9780429155666.
  6. ^ Nerio LS, Olivero-Verbel J, Stashenko E (2010). "Repellent activity of essential oils: a review". Bioresour Technol. 101 (1): 372–378. doi:10.1016/j.biortech.2009.07.048. PMID 19729299.CS1 maint: uses authors parameter (link)
  7. ^ a b c Russo EB (2011). "Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects". British Journal of Pharmacology. 163 (7): 1344–1364. doi:10.1111/j.1476-5381.2011.01238.x. PMC 3165946. PMID 21749363.
  8. ^ Köse EO, Deniz İG, Sarıkürkçü C, Aktaş Ö, Yavuz M (2010). "Chemical composition, antimicrobial and antioxidant activities of the essential oils of Sideritis erythrantha Boiss. and Heldr. (var. erythrantha and var. cedretorum P.H. Davis) endemic in Turkey". Food and Chemical Toxicology. 48 (10): 2960–2965. doi:10.1016/j.fct.2010.07.033. PMID 20670669.
  9. ^ Özek G, Demirci F, Özek T, Tabanca N, Wedge DE, Khan SI, et al. (2010). "Gas chromatographic-mass spectrometric analysis of volatiles obtained by four different techniques from Salvia rosifolia Sm., and evaluation for biological activity". Journal of Chromatography A. 1217 (5): 741–748. doi:10.1016/j.chroma.2009.11.086. PMID 20015509.
  10. ^ Hillig KW (2004). "A chemotaxonomic analysis of terpenoid variation in Cannabis". Biochemical Systematics and Ecology. 32 (10): 875–891. doi:10.1016/j.bse.2004.04.004.
  11. ^ Kasuan N (2013). "Extraction of Citrus hystrix D.C. (Kaffir Lime) Essential Oil Using Automated Steam Distillation Process: Analysis of Volatile Compounds" (PDF). Malyasian Journal of Analytical Sciences. 17 (3): 359–369.
  12. ^ "alpha-Pinene - Compound Summary". PubChem. NCBI. Retrieved 14 Nov 2017.
  13. ^ Neuenschwander U, Guignard F, Hermans I (2010). "Mechanism of the Aerobic Oxidation of α-Pinene". ChemSusChem (in German). 3 (1): 75–84. doi:10.1002/cssc.200900228. PMID 20017184.
  14. ^ Raman V, Sivasankaralingam V, Dibble R, Sarathy SM (2016). "α-Pinene - A High Energy Density Biofuel for SI Engine Applications". SAE Technical Paper. SAE Technical Paper Series. 1. doi:10.4271/2016-01-2171.