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Hemp & Cannabinoid Science / Terpene Monographs / Gamma-Curcumene

Gamma-Curcumene

A bisabolane-type sesquiterpene hydrocarbon reported at 15.76 percent of Helichrysum odoratissimum oil. Structurally placed, pharmacologically almost undocumented as an isolated compound.

At a glance

Structure classsesquiterpene hydrocarbon, bisabolane type โ€” the curcumene series related to turmeric sesquiterpenes
Molecular formulaC15H24
Molar massabout 204.36 g/mol
Related compoundsalpha-curcumene, beta-curcumene, ar-curcumene, and the turmeric turmerones; ar-curcumene is the aromatic member and is much better studied
Boiling pointnot reliably tabulated in any source available to this shelf; expect the sesquiterpene region
Vaporization bandnot measured. By analogy with other sesquiterpenes, expect the 175 to 200 degrees Celsius (347 to 392 degrees Fahrenheit) band. This is an inference, not a measurement
Documented receptor or enzyme activityNONE for gamma-curcumene specifically that this shelf can cite
Evidence levelLOW. Structurally well placed; pharmacologically undocumented as an isolated compound

On this page

What gamma-curcumene is contested

Gamma-curcumene is a sesquiterpene hydrocarbon, C15H24 at about 204.36 g/mol, belonging to the bisabolane structural family โ€” the same skeletal group as alpha-, beta- and ar-curcumene and, more distantly, the turmerones of turmeric. The curcumene name comes from Curcuma, and the group is best known from turmeric volatile oil, where it sits alongside the far more famous non-volatile curcuminoids. Note the trap in that sentence: curcumene and curcumin are unrelated compounds that share a plant and three syllables. Curcumin is a non-volatile diarylheptanoid polyphenol with a very large research literature; gamma-curcumene is a volatile sesquiterpene hydrocarbon with almost none. Do not transfer a claim from one to the other, and be alert for consumer copy that does.

Contested โ€” caveat. The structural class assignment is from reference compilation rather than from a primary structural paper cited here. The commonly quoted formula C15H24 and mass about 204.4 g/mol follow from the class and are consistent across compound databases.

Sources: Compiled from public compound databases (PubChem 2026* ยท Van Kush Family Research Institute (operator) 2026*

Why it is on this shelf contested

Gamma-curcumene has a page because the operator's Temple Pharmacopoeia records it at 15.76 percent of the essential oil of Helichrysum odoratissimum, making it the third major constituent of that material after alpha-pinene (up to 43 percent) and 1,8-cineole (17.44 percent). Two of those three compounds have substantial pharmacology sections on this shelf. The third does not, and a reader working with H. odoratissimum oil deserves to know which is which rather than to infer that everything in a well-studied oil is itself well studied. The South African Helichrysum review literature describes a varied sesquiterpenoid chemistry across the genus which is consistent with curcumene-type compounds being present; this shelf does not claim that the review reports this specific figure.

Contested โ€” caveat. Single-source quantitative figure from an internal operator document, describing one analysis of one population.

Sources: Van Kush Family Research Institute (operator) 2026* ยท Lourens ACU 2008

What is NOT known contested

There is no documented receptor or enzyme target for gamma-curcumene as an isolated compound. There is no animal behavioural, analgesic or anti-inflammatory study on the isolated compound that this shelf can cite. There is no toxicology and no sensitisation data. There is no reliably tabulated boiling point or vapour pressure, so the vaporization band on this page is an inference from compound class rather than a measurement. The nearest relative with a real literature is ar-curcumene, the aromatic member of the series, which appears in antimicrobial and antiproliferative in-vitro reports โ€” and activity in ar-curcumene is not evidence about gamma-curcumene. Much of what circulates about "curcumene" activity is in fact about turmeric oil as a mixture, about the turmerones, or about curcumin, and attributing any of it to gamma-curcumene is an error. The same reference-standard point applies as for faurinone: without a certified standard, a reported percentage is most likely a mass-spectral library match with a relative area percent rather than a true quantitation, and a purchaser relying on that figure should ask the lab which it is.

Contested โ€” caveat. This section documents an absence of evidence, not a finding of inactivity or of safety. Treat gamma-curcumene as an uncharacterised major constituent of the material.

Sources: Compiled from public compound databases (PubChem 2026* ยท Van Kush Family Research Institute (operator) 2026*

Industry notes

For a formulator, H. odoratissimum oil is a material in which roughly a sixth of the volatile fraction is an uncharacterised sesquiterpene. Document that as a known-unknown. For a lab tech, the curcumene isomers are a classic identification hazard: several isomers with the same nominal mass and similar spectra, so library matching alone will not reliably distinguish gamma- from alpha-, beta- or ar-curcumene, and the assignment should be qualified on the report unless a standard was run. For a researcher, this is the same opening as faurinone and the same first steps: authentic standard, physical constants, verifiable structural identifier.

Sources: Van Kush Family Research Institute (operator) 2026* ยท Compiled from public compound databases (PubChem 2026*

See also

References

  1. Compiled from public compound databases (PubChem, NIST WebBook) and supplier specification sheets (2026) Physical constants for terpenes and terpenoids: formula, molar mass, atmospheric boiling point Reference compilation; individual values vary between sources and are given as ranges here. [identifier unverified]
  2. Van Kush Family Research Institute (operator) (2026) Temple Pharmacopoeia knowledgebase: botanical preparations, extraction science and formulation frameworks Internal operator document, compiled January 2026. [identifier unverified]
  3. Lourens ACU, Viljoen AM, van Heerden FR (2008) South African Helichrysum species: a review of the traditional uses, biological activity and phytochemistry Journal of Ethnopharmacology 119(3):630-652. doi:10.1016/j.jep.2008.06.011

3 references, of which 2 carry no resolved identifier and are marked as such. A DOI is only recorded here when it was resolved against Crossref and the returned title matched the one printed. None was guessed.

Absence is not safety. A substance or a pair that is not in this section was not checked and is not thereby safe. This is a curated mechanism reference built from primary literature and regulatory reference works โ€” not a comprehensive interaction database, and not a substitute for a clinician or a pharmacist.

Posture

Education and harm reduction. Not medical, legal or financial advice. Every factual claim carries a source; contested and single-source claims are marked as such on the page.

The boundary. This section teaches separation, purification, formulation, dosing arithmetic and analytical chemistry with real parameters, because withholding that detail from someone who will proceed anyway is the harm this library exists to prevent. It does not publish preparative routes for converting one cannabinoid into a more intoxicating one; those are described structurally and cited to the literature, without procedures.