# Essential oil fractions of hemp profiles at different hydro-distillation periods

**Authors:** Valtcho D. Zheljazkov, Vladimir Sikora, Tess Astatkie, Ivayla Dincheva, Milica Acimović, Jelena Visković, Dragana Latković, Jay S. Noller

PMC · DOI: 10.1371/journal.pone.0331767 · PLOS One · 2025-10-29

## TL;DR

This study shows that hemp essential oils can be fractionated during distillation to separate monoterpenes early and sesquiterpenes and cannabinoids later.

## Contribution

The study introduces a method to isolate distinct hemp essential oil fractions based on distillation time for targeted chemical profiles.

## Key findings

- Most essential oil compounds were eluted early, with monoterpenes dominating the first 5 minutes of distillation.
- Sesquiterpenes and cannabinoids were concentrated in later distillation fractions, peaking after 160 minutes.
- Separating early and late fractions allows for essential oils with either high monoterpenes or high sesquiterpenes and cannabinoids.

## Abstract

The hypothesis of this study was that hemp (Cannabis sativa L.) essential oil (EO) constituents from high-cannabinoid hemp are eluted at different times during the hydro-distillation process, allowing the generation of fractions with distinct chemical profile, with or without cannabinoids. The objective was to reveal changes in the compositional profile of EO fractions captured at ten sequential distillation timeframes (DT) and a control. Regression analysis was conducted to model the relationship between DT and 20 EO compounds, classified in four groups (monoterpenes, sesquiterpenes, cannabinoids, and others (acid esters, ketone, alcohol)) using ten DT values (5, 10, 20, 40, 80, 120, 160, 200, 240, and 280 min). The results showed that most of the EO compounds were eluted early in the distillation process, until 10 min, then the EO compounds gradually decreased until 120 min and decreased to negligible amounts after 160 min DT. Monoterpenes eluted early in the distillation process, accounting for 69.79% of the total EO collected during the 0–5 min distillation interval. After that, the monoterpenes gradually decreased to 13.77% in the 240–280 min DT, while their concentration in the 0–180 min non-stop distillation was 33.55%. Conversely, the sesquiterpenes were eluted late in the distillation process. The concentration of sesquiterpenes in the 0–5 min DT EO was 25.73%, then gradually increased to reach a plateau at 160–280 min DT (75.3–76.8%), while their concentration in the 0–180 min DT was 54.4%. The results demonstrated that hemp EO with higher concentration of monoterpenes and free of cannabinoids can be obtained by separating the initial fractions, while hemp EO with higher concentration of sesquiterpenes and cannabinoids such as cannabidiol (CBD), cannabichromene (CBC), δ8-tetrahydrocannabinol (commonly known as δ8-THC), and δ9-tetrahydrocannabinol (commonly known as δ9-THC or dronabinol) can be obtained by capturing the fraction eluted after 160 min DT.

## Linked entities

- **Chemicals:** cannabidiol (PubChem CID 644019), cannabichromene (PubChem CID 30219), dronabinol (PubChem CID 16078)

## Full-text entities

- **Chemicals:** delta8-THC (MESH:C035731), cannabinoid (MESH:D002186), EO (MESH:D009822), Monoterpenes (MESH:D039821), sesquiterpenes (MESH:D012717), CBC (MESH:C010695), delta9-THC (MESH:D013759), ketone (MESH:D007659), acid esters (-), CBD (MESH:D002185), alcohol (MESH:D000438)
- **Species:** Cannabis sativa (species) [taxon 3483]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12571300/full.md

## References

115 references — full list in the complete paper: https://tomesphere.com/paper/PMC12571300/full.md

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Source: https://tomesphere.com/paper/PMC12571300