Eucalyptol

Identity

Property Value
Preferred name Eucalyptol (1,8-Cineole)
IUPAC name 1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane
CAS number 470-82-6
PubChem CID 2758 [^5]
Chemical family Bicyclic Monoterpenoid Ether
Molecular formula C10H18O
Molecular mass 154.25 g/mol
Stereochemistry No chiral centers

Aroma and sensory character

Fresh, minty, camphoraceous, cooling sensory character.

Occurrence outside cannabis

  • Eucalyptus (Eucalyptus globulus)
  • Rosemary (Rosmarinus officinalis)
  • Tea tree (Melaleuca alternifolia)
  • Bay leaves (Laurus nobilis)

Physical properties

Property Value
Standard boiling point 176 °C
Reference pressure 101.325 kPa
Data source NIST Chemistry WebBook (SRD 69); mean of 6 determinations [^1]

Thermal-extraction context

Reported biological activity

Human evidence

A placebo-controlled double-blind trial found that oral cineole (1,8-cineole) improved symptoms and cough frequency in patients with acute bronchitis [^2]. A separate double-blind trial in COPD patients found that oral cineole (200 mg, three times daily) added to standard therapy reduced exacerbations, dyspnea, and improved lung function [^3]. Both studies evaluated oral capsules, not inhalation from a vaporizer.

Animal or laboratory evidence

Peer-reviewed reviews of eucalyptus-oil pharmacology summarize anti-inflammatory, antimicrobial, and respiratory-relief activity attributed largely to 1,8-cineole in animal and cell models 1. The underlying experiments are predominantly preclinical; human data are oral-route clinical trials, not inhaled vaporizer studies.

Traditional or anecdotal claims

Longstanding use in respiratory vapor inhalations and chest rubs.

Cannabis laboratory results

An occasional, usually minor constituent: detected in only 3 of 19 dried-flower cultivars in a Thai GC-MS survey (0.01–0.39% of identified peak area) and below detection in the rest 2. Check Lab Results for detected levels.

Sources

  1. El Shiekh RA, et al. Therapeutic applications of eucalyptus essential oils. Inflammopharmacology. 2024. doi:10.1007/s10787-024-01588-8. PMID 39499358. (Peer-reviewed review.) ↩

  2. Janta S, et al. Chemical profiling and clustering of various dried cannabis flowers. J Cannabis Res. 2024. doi:10.1186/s42238-024-00252-w. PMID 39639406. ↩