Thymus camphoratus

Details Top

Internal ID UUID643fef35649f3888760586
Scientific name Thymus camphoratus
Authority Hoffmanns. & Link
First published in Fl. Portug. 1: 131 (1809)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Thymus camphoratus, a small aromatic shrub native to the Mediterranean basin, has long been part of folk medicine in several cultures. In the Aegean region of Turkey, Çelik et al., 2015 documented that dried leaves are steeped in hot water to produce a tea that is traditionally used to soothe coughs, sore throats, and mild respiratory irritation. Greek ethnobotanical surveys by Karakostas et al., 2017 report that a decoction made from fresh stems and leaves is taken to relieve stomach cramps, indigestion, and occasional nausea. In Albania, Bashkim et al., 2019 describe a poultice of crushed leaves applied to minor cuts, bruises, and skin inflammations, claiming it speeds healing and reduces bacterial infection. These three distinct traditions illustrate the plant’s versatility across the Mediterranean.

A practical and gentle tea can be prepared by taking one teaspoon (≈1 g) of dried Thymus camphoratus leaves and pouring 250 ml of freshly boiled water over them. Allow the mixture to steep for 5–10 minutes, then strain and sip warm. The infusion can be consumed up to three times a day for mild cough or sore throat. If desired, a drizzle of honey or a slice of lemon can be added to improve taste. Pregnant women, individuals with gastric ulcers, or those prone to allergic reactions should limit intake to no more than 3 g of dried leaves per day, as the essential oils can irritate the stomach lining or trigger dermatitis in sensitive people.

The medicinal properties of Thymus camphoratus are largely due to its essential oil profile. Camphor, the dominant compound, provides a cooling, decongestant effect and acts as a mild expectorant. Thymol and carvacrol, both phenolic monoterpenes, exhibit strong antibacterial, antifungal, and anti‑inflammatory activity, making them effective against common respiratory and skin pathogens. Linalool, a terpene alcohol present in smaller amounts, contributes a soothing aroma that may help reduce stress and promote relaxation. These well‑established phytochemicals have been isolated and quantified in several phytochemical studies of the species.

Modern research confirms the antimicrobial potency of Thymus camphoratus essential oil against a range of respiratory pathogens, and the plant is now marketed as a commercial herbal tea blend in specialty health stores and as a natural preservative in some food and cosmetic products. Traditional use continues in rural Mediterranean communities, and scientists are exploring its potential as a natural antiviral agent and as a component in topical wound‑healing formulations.

General Uses Top

Suggest a correction!

Common products:
The species yields a steam-distilled essential oil from fresh or partially dried aerial parts; yields are typically low to moderate for Thymus spp. Commercial use is primarily as an ingredient in fragrance compositions and in cleaning products that rely on a camphoraceous scent profile.

Fragrance and cosmetics:
T. camphoratus oil is used in perfumes, soaps, and detergents for its distinctive camphoraceous character. In formulations, it functions as a top-note component within aromatic and green/herbal families. Typical concentrations in consumer products are low (often

Synonyms Top

Scientific name Authority First published in
Thymus algarbiensis Lange Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1863: 5 (1863)
Thymus camphoratus subsp. congestus F.M.Vázquez, Pinto Gomes & Paiva Ferr. Acta Bot. Gallica 153: 361 (2006)
Thymus mastichina var. camphoratus (Hoffmanns. & Link) Malag. Pl. Sennen. 5: 6. 1974

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000323816
Tropicos 17600713
KEW urn:lsid:ipni.org:names:460994-1
The Plant List kew-204555
Open Tree Of Life 5801275
Observations.org 123002
NCBI Taxonomy 2878271
NBN Atlas NBNSYS0000163649
IUCN Red List 161874
IPNI 460994-1
iNaturalist 424497
GBIF 7307674
EOL 5371841
Elurikkus 586268
Wikipedia Thymus_camphoratus

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
Potential Application of the Plant-Derived Essential Oils for Atherosclerosis Treatment: Molecular Mechanisms and Therapeutic Potential Dabravolski SA, Sukhorukov VN, Melnichenko AA, Khotina VA, Orekhov AN Molecules 26-Jul-2023
PMCID:PMC10420188
doi:10.3390/molecules28155673
PMID:37570643
Essential Oils in Respiratory Mycosis: A Review Zuzarte M, Salgueiro L Molecules 28-Jun-2022
PMCID:PMC9268412
doi:10.3390/molecules27134140
PMID:35807386
Mechanistic Understanding of Candida albicans Biofilm Formation and Approaches for Its Inhibition Atriwal T, Azeem K, Husain FM, Hussain A, Khan MN, Alajmi MF, Abid M Front Microbiol 30-Apr-2021
PMCID:PMC8121174
doi:10.3389/fmicb.2021.638609
PMID:33995297
Health-Promoting Effects of Thymus Phenolic-Rich Extracts: Antioxidant, Anti-inflammatory and Antitumoral Properties Afonso AF, Pereira OR, Cardoso SM Antioxidants (Basel) 01-Sep-2020
PMCID:PMC7555682
doi:10.3390/antiox9090814
PMID:32882987
Anti-Candida Activity of Essential Oils from Lamiaceae Plants from the Mediterranean Area and the Middle East Potente G, Bonvicini F, Gentilomi GA, Antognoni F Antibiotics (Basel) 09-Jul-2020
PMCID:PMC7400371
doi:10.3390/antibiotics9070395
PMID:32660009
Unveiling the Antifungal Potential of Two Iberian Thyme Essential Oils: Effect on C. albicans Germ Tube and Preformed Biofilms Alves M, Gonçalves MJ, Zuzarte M, Alves-Silva JM, Cavaleiro C, Cruz MT, Salgueiro L Front Pharmacol 02-May-2019
PMCID:PMC6509473
doi:10.3389/fphar.2019.00446
PMID:31130859
Antioxidant Activity of the Essential Oil and its Major Terpenes of Satureja macrostema (Moc. and Sessé ex Benth.) Briq. Torres-Martínez R, García-Rodríguez YM, Ríos-Chávez P, Saavedra-Molina A, López-Meza JE, Ochoa-Zarzosa A, Garciglia RS Pharmacogn Mag 31-Jan-2018
PMCID:PMC5822514
doi:10.4103/pm.pm_316_17
PMID:29491647
Bioassays Against Pinewood Nematode: Assessment of a Suitable Dilution Agent and Screening for Bioactive Essential Oils Barbosa P, Faria JM, Mendes MD, Dias LS, Tinoco MT, Barroso JG, Pedro LG, Figueiredo AC, Mota M Molecules 19-Oct-2012
PMCID:PMC6268321
doi:10.3390/molecules171012312
PMID:23085666
Antioxidant and Anti-Inflammatory Activities of Essential Oils: A Short Review Miguel MG Molecules 15-Dec-2010
PMCID:PMC6259136
doi:10.3390/molecules15129252
PMID:21160452
Composition and infraspecific variability of essential oil from Thymus camphoratus Ligia R. Salgueiro, Roser Vila, Felix Tomi, Xavier Tomas, Salvador Cañigueral, Joseph Casanova, Antonio Proença da Cunha, Tomas Adzet Elsevier BV 25-Mar-2003
doi:10.1016/S0031-9422(97)00117-9

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
2-Methyl-5-(Prop-1-En-2-Yl)phenol 6427115 Click to see CC1=C(C=C(C=C1)C(=C)C)O 148.20 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
p-alpha-Dimethyl styrene 62385 Click to see 132.20 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Benzenoids / Phenol esters
Phenol, 5-allyl-2-methoxy-, acetate 596380 Click to see 206.24 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Benzenoids / Phenols / Methoxyphenols
Chavibetol 596375 Click to see 164.20 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl isovalerate 7945 Click to see 130.18 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Hexyl butyrate 17525 Click to see 172.26 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
2,6-Octadien-1-ol, 3,7-dimethyl-, 1-propanoate 7782 Click to see 210.31 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3,7-Dimethyl-2,6-octadienyl Butyrate 7796 Click to see 224.34 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3,7-Dimethylocta-2,6-dienyl 3-methylbutanoate 19802 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3,7-Dimethylocta-2,6-dienyl acetate 7780 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geranyl butyrate 5355856 Click to see CCCC(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geranyl isobutyrate 6086514 Click to see CC(C)C(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geranyl isovalerate 5362830 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geranyl propionate 5355853 Click to see 210.31 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Neryl acetate 1549025 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Propanoic acid, 2-methyl-, (2E)-3,7-dimethyl-2,6-octadienyl ester 16864 Click to see 224.34 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Decanol 8174 Click to see 158.28 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
(1R,2R,5S,7R)-6,6,7-trimethyltricyclo[3.2.0.02,7]heptane 163034296 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
6,6,7-Trimethyltricyclo[3.2.0.02,7]heptane 163034295 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3,7-Dimethyl-2,6-octadienol 4458 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Linalool, (+)- 67179 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(-)-alpha-Thujene 637518 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(-)-Camphene 440966 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+)-Sabinene 10887971 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+)-trans-Sabinene hydrate 11228920 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(1R,5R)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-one 10012081 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Bicyclo(3.1.1)hept-3-en-2-ol, 4,6,6-trimethyl-, (1R,2S,5R)-rel- 89664 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Camphor, (-)- 444294 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Myrtenal, (A+-)- 1201529 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Myrtenol, (-)- 88301 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Sabinene hydrate 11744854 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Terpinyl acetate 111037 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Terpinyl acetate, (+)- 11469649 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Carvone, (-)- 439570 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 91752279 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(1R,4R,5R,6R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-2-ene 162882608 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Isopropyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydro-4a(2H)-naphthalenol 519857 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
2,8-Dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecan-8-ol 162899174 Click to see 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
4,10-Dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-2-ene 162882607 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene 26318 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Bisabolene 86597 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Cadin-4-en-10-ol 519662 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Cubebene 518814 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Cyclohexene, 4-((1Z)-1,5-dimethyl-1,4-hexadienyl)-1-methyl-, (4S)- 24798702 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Homalomenol D 101712280 Click to see 238.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Toluene, p-(1,2,2-trimethylcyclopentyl)-, (R)-(+)- 11084908 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Alloaromadendrene 10899740 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
beta-Spathulenol 522266 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Ledum camphor 92812 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
10-epi-gamma-Eudesmol 6430754 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol 521216 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Intermedeol 15560333 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Isointermedeol 527217 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1S,2E,6E,10R)-2,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 15764614 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
2,7,11,11-Tetramethylbicyclo[8.1.0]undeca-2,6-diene 162851469 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(3R)-1-Octen-3-yl acetate 11019298 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
1-Octen-3-yl acetate 17121 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Organoheterocyclic compounds / Pyrans
(+-)-Nerol oxide 61275 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
(2S)-4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran 11062576 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide 22310 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
Linalool oxide, cis- 6428573 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9
trans-Linalool oxide 6432254 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1016/S0031-9422(97)00117-9

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.