# Formation and transfer patterns of key aroma compounds in cigar tobacco based on SBSE-GC-O-MS, pyrolysis-GC-O-MS and flue gas analysis correlation studies

**Authors:** Xue Wu, Xinhua Song, Tianze Liu, Xu Wang, Chao Wang, Wentao Zhao, Yuqing Dou

PMC · DOI: 10.3389/fchem.2026.1755255 · Frontiers in Chemistry · 2026-02-17

## TL;DR

This study explores how key aroma compounds in cigars form and transfer from tobacco leaves to smoke using advanced analytical techniques.

## Contribution

The paper introduces a novel combined analytical strategy using SBSE, pyrolysis, and smoke capture to trace aroma compound evolution in cigars.

## Key findings

- Cigar tobacco leaves' aroma is dominated by terpenes and carotenoid degradation products with a 'green and citrus fruit' profile.
- Pyrolysis transforms the aroma into a 'toasty sweetness and roasted nutty' profile centered on furan and pyrazine compounds.
- Smoke balances sweet, green, and fruity notes, with specific compounds showing strong correlations across stages.

## Abstract

The aromatic quality of cigars represents their core value, arising from the thermal transformation and migration of inherent components within tobacco leaves—a highly complex dynamic process. To systematically trace the evolution of key aroma compounds from tobacco leaves to smoke, this study pioneered a combined strategy of Stirred Barrel Sorption Extraction (SBSE), Pyrolysis (PY), and mainstream smoke capture. Utilizing Gas Chromatography-Olfactometry-Mass Spectrometry (GC-O-MS) coupled with Odor Activity Values (OAV) and correlation network analysis, a comprehensive analysis was conducted. Results revealed: The intrinsic aroma of cigar tobacco leaves is dominated by terpenes and carotenoid degradation products, presenting a “green and citrus fruit” profile. Pyrolysis fundamentally transforms the aroma spectrum into a “toasty sweetness and roasted nutty” profile centered on furan and pyrazine compounds. While smoke exhibited a balanced profile blending sweet, green, and fruity notes. Quantitative DTE revealed highly efficient nicotine transfer (30%), pyrazine pyrolysis enrichment (40%–50%), and phenol thermal generation (Thermal Generation Factor >8), with only 44% of Neophytadiene entering the smoke. Correlation analysis revealed that Phenol and 2-methoxy- in pyrolysis products positively correlated with multiple terpenes, aldehydes, and nitrogen-containing heterocyclic compounds in tobacco leaves, while Phenol showed negative correlations. The roasted aroma marker furfural in smoke significantly correlated with neophytadiene, a carotenoid degradation product in tobacco leaves. While the characteristic nutty aroma component 2,6-dimethylpyrazine showed a strong positive correlation with α-terpineol acetate in the tobacco leaf itself. This study elucidates the formation mechanism of cigar characteristic aromas at the molecular level, providing important theoretical basis for precise quality evaluation, scientific formulation design, and process optimization of cigar tobacco.

## Linked entities

- **Chemicals:** furan (PubChem CID 8029), pyrazine (PubChem CID 9261), phenol (PubChem CID 996), neophytadiene (PubChem CID 10446), furfural (PubChem CID 7362), 2,6-dimethylpyrazine (PubChem CID 7938), α-terpineol acetate (PubChem CID 111037)

## Full-text entities

- **Genes:** aldehyde dehydrogenase [NCBI Gene 107777569]
- **Chemicals:** catechols (MESH:D002396), 3-Pyridinol (MESH:C023500), ATP (MESH:D000255), Lignin (MESH:D008031), erythrulose-4-phosphate (MESH:C042347), cycloalkenes (MESH:D003516), methyl tert-butyl ether (MESH:C043243), hexanal (MESH:C010463), lipids (MESH:D008055), furfural (MESH:D005662), Cotinine (MESH:D003367), heterocyclic compounds (MESH:D006571), hydrogen (MESH:D006859), alcohols (MESH:D000438), GC (MESH:C057580), 2-methoxytoluene (MESH:C428434), Terpineol acetate (MESH:C019564), 3,7,11,15-Tetramethyl-2-hexadecen-1-ol (MESH:C549873), flavonoids (MESH:D005419), Pyrazine (MESH:D011719), diterpenes (MESH:D004224), Indole (MESH:C030374), hydroxyacetone (MESH:C004433), helium (MESH:D006371), furan (MESH:C039281), 1-(acetyloxy)- (acetoxyacetone (-), ethyl acetate (MESH:C007650), n-butanol (MESH:D020001), 4-Pyridinol (MESH:C534143), Pyridine (MESH:C023666), 2,6-dimethoxyphenol (MESH:C010120), hexane (MESH:D006586), linalool (MESH:C018584), amino acids (MESH:D000596), 2-Methoxyphenol (MESH:D006139), Hydroxylamine (MESH:D019811), Nicotine (MESH:D009538), n-heptadecane (MESH:C016486), 2-Propanone (MESH:D000096), monoterpene (MESH:D039821), Cyclohexene (MESH:C052568), Propylene Glycol (MESH:D019946), Glycidol (MESH:C004312), shikimic acid (MESH:D012765), Furaneol (MESH:C058427), (+)-alpha-Pinene (MESH:C005451), carotenoid (MESH:D002338), phosphoenolpyruvate (MESH:D010728), Megastigmatrienone (MESH:C549856), Phenol (MESH:D019800), water (MESH:D014867), benzenes (MESH:D001554), Phenylethyl Alcohol (MESH:D010626), Nonanal (MESH:C008664), terpenes (MESH:D013729), indoles (MESH:D007211), 1,2-dihydroxybenzene (MESH:C034221), aromatic alcohols (MESH:D019905), Triacetin (MESH:D014215), acetic acid (MESH:D019342)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], Citrus x limon (lemon, species) [taxon 2708]
- **Mutations:** C-93  C, Start at 40, C +- 2  C, C-174  C, C-216  C

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12952821/full.md

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Source: https://tomesphere.com/paper/PMC12952821