Ocimene

Identity

Property Value
Preferred name β-Ocimene
IUPAC name 3,7-dimethylocta-1,3,6-triene (β-ocimene)
CAS number 13877-91-3 (β-ocimene, unspecified E/Z)
PubChem CID 18756 [^3]
Chemical family Acyclic Monoterpene
Molecular formula C10H16
Molecular mass 136.23 g/mol
Stereochemistry α- and β-ocimene are position isomers kept as distinct identities (α-ocimene: CAS 6874-44-8). β-Ocimene additionally exists as (E)/(Z) geometric isomers, e.g. (3E)-trans-β-ocimene (CAS 3779-61-1); this record covers β-ocimene, CAS 13877-91-3

Aroma and sensory character

Sweet, floral, herbaceous, woody, and tropical scent.

Occurrence outside cannabis

  • Basil (Ocimum basilicum)
  • Mint (Mentha species)
  • Orchids (Orchidaceae)
  • Mango (Mangifera indica)

Physical properties

Property Value
Standard boiling point 176 °C (predicted; unconfirmed by NIST) [^1]
Reference pressure 101.325 kPa
Data source Predicted/estimated value; NIST WebBook (CAS 13877-91-3) lists no boiling point

Thermal-extraction context

Reported biological activity

Human evidence

No rigorous human clinical studies evaluating isolated vaporized ocimene exist to date.

Animal or laboratory evidence

In rodent and cell models, ocimene reduced inflammatory signaling and protected against NSAID (indomethacin)-induced gastric ulceration, with analgesic activity in formalin and acetic-acid pain assays 1. These are preclinical observations at non-inhalation doses; antifungal claims remain without a located primary source in this archive.

Traditional or anecdotal claims

Herbal tea component recognized in traditional perfumery and pest defense.

Cannabis laboratory results

Measured as (E)-β-ocimene at 191–1,382 µg/g dry weight in four of six cultivars (not detected in the remaining two), with extreme plant-to-plant variation; typically <5% of total terpenes 2. See Lab Results for batch data.

Sources

  1. Attenuation of nonsteroidal anti-inflammatory drug-induced gastric ulcers by ocimene. ACS Pharmacol Transl Sci. 2025. doi:10.1021/acsptsci.4c00639. PMID 40109750. ↩

  2. Booth JK, et al. Terpene synthases and terpene variation in Cannabis sativa. Plant Physiol. 2020;184(1):130–147. PMID 32591428; Joy N, et al. A Validated GC-MS Method for Major Terpenes Quantification in Cannabis sativa L. Essential Oil. 2025. PMC12670203; PMID 40042239. ↩