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.

Traditional users of Lavandula latifolia (broad‑leaved or spike lavender) have recorded several therapeutic preparations that rely on infusions, decoctions, macerations, or poultices. In the sun‑baked fields of southern Spain, farmers traditionally brew a mild tea from the fresh aerial parts—young stems, leaves and flower spikes—for occasional digestive upset and to calm nervous tension (Marrero et al., 2020). Across the Alps of northern Italy, healers macerate dried leaf and flower material in warm water for 24 hours to produce a soothing decoction taken before bedtime to ease insomnia (Rossi & Fiore, 2018). On the Greek islands, a poultice of crushed, fresh leaves applied directly to bruises or minor skin irritations has been a household remedy for generations (Katsaros et al., 2019). In each case the preparation utilizes only the green aerial tissues of the plant.

One practical recipe that captures the most common preparation is a gentle herbal tea: place roughly 2 g of dried leaves and flower spikes in a ceramic teapot, pour 250 ml of freshly boiled water over them, cover and let steep for 5–10 minutes before straining. The resulting infusion is lightly aromatic, with a camphor‑spiced taste that many find soothing for occasional stomach cramps or mild anxiety. Safety note: the camphor content in L. latifolia can be irritating to the gastrointestinal tract in high doses; limit consumption to one cup per day and avoid use during pregnancy or by individuals with known camphor sensitivity.

The therapeutic activity of these preparations is plausibly linked to the plant’s well‑documented phytochemicals. The essential oil of L. latifolia is rich in camphor and 1,8‑cineole (eucalyptol), compounds noted for their antispasmodic and expectorant actions, and also contains linalool and borneol, which contribute mild sedative and anti‑inflammatory effects (Gómez‑Serranillos et al., 2012). These constituents help explain the traditional use of the tea for digestive relief and the poultice’s capacity to calm superficial inflammation.

Modern relevance remains robust: scientific investigations continue to explore the antimicrobial and analgesic potential of L. latifolia’s essential oil, and the plant is commercially cultivated for both its oil and dried herbal material, keeping the age‑old tea and poultice traditions alive in contemporary herbal markets.

General Uses Top

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Common products:
- Essential oil (“spike lavender oil”) obtained by hydrodistillation of the aerial parts.

Industrial and craft applications:
- Fragrance and flavor raw material for soaps, detergents, cleaners, and household aerosols where a penetrating, medicinal-herbal note is desired.

Food and beverages (non-medicinal):
- Flavoring for alcoholic beverages and liqueurs; occasionally included in spice blends as a minor flavoring ingredient.

Fragrance and cosmetics:
- Used in perfumery as a top–heart note and to add freshness and lift to lavender accords.
- Employed in the fragrance industry as a source of natural camphor and linalool for aroma compositions.

Properties relevant to use:
- Spike lavender oil is characterized by a high camphor content (typically 20–35%) with linalool, 1,8-cineole, and bornyl acetate as notable constituents, conferring a sharp, fresh, and medicinal aroma.
- Complies with ISO 3515 (Spike lavender oil—specification), defining limits for specific gravity, optical rotation, refractive index, acid value, and ester value.

Standards and regulation:
- ISO 3515 specifies quality requirements and test methods for authentic spike lavender oil in commerce; quality is often monitored by gas chromatography in accordance with ISO 11014 and ISO 7609 for major constituents.

Sustainability and sourcing:
- Spike lavender oil is primarily produced from wild-harvested Lavandula latifolia in Spain, France, and Italy; established supply chains incorporate artisanal distillation and quality testing against ISO 3515 to ensure consistent oil profiles.

Synonyms Top

Scientific name	Authority	First published in
Lavandula angustifolia	Moench	Methodus : 389 (1794)
Lavandula erigens	Jord. & Fourr.	Brev. Pl. Nov. 2: 88 (1868)
Lavandula hybrida	Reverchon ex Briq.	Lab. Alp. Mar. : 469 (1895)
Lavandula inclinans	Jord. & Fourr.	Brev. Pl. Nov. 2: 88 (1868)
Lavandula interrupta	Jord. & Fourr.	Brev. Pl. Nov. 2: 89 (1868)
Lavandula major	Garsault	Fig. Pl. Méd. : t. 330 (1764)
Lavandula ovata	Steud.	Nomencl. Bot. , ed. 2, 2: 17 (1841)
Lavandula spica	Cav.	Descr. Pl. : 69 (1801)
Lavandula spica var. latifolia	L.	Sp. Pl. 572. 1753
Lavandula cladophora	Gand.	Dec. Pl. Nov. 1: 38 (1875)
Lavandula guinandii	Gand.	Dec. Pl. Nov. 1: 38 (1875)
Lavandula decipiens	Gand.	Dec. Pl. Nov. 1: 38 (1875)
Lavandula latifolia var. tomentosa	Briq.	Lab. Alp. Mar. 472. 1895
Lavandula latifolia var. erigens	(Jord. & Fourr.) Nyman	Consp. Fl. Eur. 572. 1881
Lavandula spica var. vulgaris	Ging.	Hist. Nat. Lavand. : 154 (1826)
Lavandula latifolia var. vulgaris	Briq.	Lab. Alp. Mar. : 472 (1895)
Lavandula latifolia var. erigens	(Jord. & Fourr.) Rouy	Fl. France 11: 257 (1909)
Lavandula spica var. ramosa	DC.	Fl. Franç. , éd. 3, 6: 379 (1815)
Lavandula spica subsp. latifolia	Bonnier & Layens	Tabl. Syn. Pl. Vasc. France 247 (1894)

Common names Top

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Filter by language:

Language	Common/alternative name
English	spike lavendar
English	spike lavender
English	broadleaved lavender
Spanish	barbayo
Spanish	espigol
Spanish	arnica de monte
Spanish	alhusema
Spanish	jucena
Spanish	boja esplieguera
Spanish	espígol
Spanish	espriego
Spanish	jalveo
Spanish	respliego
Spanish	lucema
Spanish	lavándula
Arabic	خزامى عريضة الورق
Azerbaijani	enliyarpaq lavanda
Bulgarian	широколистна лавандула
br	lavand-bras
Catalan	barballó
Catalan	espígol comú
German	breitblättriger lavendel
German	speik-lavendel
Persian	لاواندولا لاتیفولیا
French	lavande aspic
French	spic
Armenian	Իլենի լայնատերև
Russian	Лаванда широколистная
Urdu	اسطو خودوس پرتگالی
Chinese	宽叶薰衣草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - France
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000224181
UNII	45396ETX3Y
USDA Plants	LALA13
Tropicos	17600105
INPN	105312
Flora of Italy	4663
KEW	urn:lsid:ipni.org:names:449051-1
The Plant List	kew-109033
Open Tree Of Life	355951
Observations.org	131493
NCBI Taxonomy	39331
NBN Atlas	NHMSYS0000460197
IUCN Red List	203245
IPNI	449051-1
iNaturalist	371559
GBIF	2927304
Freebase	/m/0g9t4p3
EPPO	LAVLA
EOL	590824
Elurikkus	335861
USDA GRIN	21680
Wikipedia	Lavandula_latifolia
PFAF	Lavandula latifolia

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

Disclosing the Functional Potency of Three Oxygenated Monoterpenes in Combating Microbial Pathogenesis: From Targeting Virulence Factors to Chicken Meat Preservation

Akermi S, Chaari M, Elhadef K, Fourati M, Chakchouk Mtibaa A, Agriopoulou S, Smaoui S, Mellouli L

Foods

21-Mar-2024

PMCID:	PMC10970324
doi:	10.3390/foods13060965
PMID:	38540955

Identification and expression analysis of TPS family gene in Cannabis sativa L

Xu J, Kong L, Ren W, Wang Z, Tang L, Wu W, Liu X, Ma W, Zhang S

Heliyon

16-Mar-2024

PMCID:	PMC10966592
doi:	10.1016/j.heliyon.2024.e27817
PMID:	38545150

Intraspecific differentiation of Lindera obtusiloba as revealed by comparative plastomic and evolutionary analyses

Tian X, Guo J, Song Y, Yu Q, Liu C, Fu Z, Shi Y, Shao Y, Yuan Z

Ecol Evol

11-Mar-2024

PMCID:	PMC10927362
doi:	10.1002/ece3.11119
PMID:	38469045

Enhancing Essential Oil Extraction from Lavandin Grosso Flowers via Plasma Treatment

Molina R, López-Santos C, Balestrasse K, Gómez-Ramírez A, Sauló J

Int J Mol Sci

17-Feb-2024

PMCID:	PMC10889515
doi:	10.3390/ijms25042383
PMID:	38397059

Transcriptome and volatile compounds analyses of floral development provide insight into floral scent formation in Paeonia lactiflora ‘Wu Hua Long Yu’

Zhao Q, Zhang M, Gu L, Yang Z, Li Y, Luo J, Zhang Y

Front Plant Sci

16-Feb-2024

PMCID:	PMC10904628
doi:	10.3389/fpls.2024.1303156
PMID:	38434428

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Recent Advances in Chemistry and Antioxidant/Anticancer Biology of Monoterpene and Meroterpenoid Natural Product

Barras BJ, Ling T, Rivas F

Molecules

04-Jan-2024

PMCID:	PMC10780832
doi:	10.3390/molecules29010279
PMID:	38202861

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023

Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A

EFSA J

15-Dec-2023

PMCID:	PMC10722330
doi:	10.2903/j.efsa.2023.8477
PMID:	38107375

Fish Scale Gelatin Nanofibers with Helichrysum italicum and Lavandula latifolia Essential Oils for Bioactive Wound-Healing Dressings

Gaidau C, Râpă M, Stanca M, Tanase ML, Olariu L, Constantinescu RR, Lazea-Stoyanova A, Alexe CA, Tudorache M

Pharmaceutics

28-Nov-2023

PMCID:	PMC10747005
doi:	10.3390/pharmaceutics15122692
PMID:	38140033

Anxiety-Reducing Effects of Lavender Essential Oil Inhalation: A Systematic Review

Yoo O, Park SA

Healthcare (Basel)

17-Nov-2023

PMCID:	PMC10671255
doi:	10.3390/healthcare11222978
PMID:	37998470

Alginate-Based Hydrogels Enriched with Lavender Essential Oil: Evaluation of Physicochemical Properties, Antimicrobial Activity, and In Vivo Biocompatibility

Rusu AG, Niță LE, Roșca I, Croitoriu A, Ghilan A, Mititelu-Tarțău L, Grigoraș AV, Crețu BE, Chiriac AP

Pharmaceutics

09-Nov-2023

PMCID:	PMC10675056
doi:	10.3390/pharmaceutics15112608
PMID:	38004586

Impact of the Drying Procedure and Botanical Origin on the Physico-Chemical and Potentially Bioactive Properties of Honey Powders

Cantero L, González-Ceballos L, Vallejos S, Puertas G, Fernández-Muiño MA, Sancho MT, Osés SM

Foods

31-Oct-2023

PMCID:	PMC10650056
doi:	10.3390/foods12213990
PMID:	37959109

Antioxidant and antimicrobial effects of essential oils from two salvia species with in vitro and in silico analysis targeting 1AJ6 and 1R4U proteins

Maache S, Zbadi L, Ghouizi AE, Soulo N, Saghrouchni H, Siddique F, Sitotaw B, Salamatullah AM, Nafidi HA, Bourhia M, Lyoussi B, Elarabi I

Sci Rep

28-Aug-2023

PMCID:	PMC10462652
doi:	10.1038/s41598-023-41178-2
PMID:	37640782

Lavandula austroapennina: Assessment of the Antiviral Activity of Lipophilic Extracts from Its Organs

Chianese A, Gravina C, Morone MV, Ambrosino A, Formato M, Palma F, Foglia F, Nastri BM, Zannella C, Esposito A, De Filippis A, Piccolella S, Galdiero M, Pacifico S

Viruses

28-Jul-2023

PMCID:	PMC10457779
doi:	10.3390/v15081648
PMID:	37631991

Recent trends of machine learning applied to multi-source data of medicinal plants

Zhang Y, Wang Y

J Pharm Anal

25-Jul-2023

PMCID:	PMC10785154
doi:	10.1016/j.jpha.2023.07.012
PMID:	38223450

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Hexyl butyrate	17525	Click to see	172.26	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethylhexadec-2-en-1-ol	145386	Click to see	296.50	unknown	https://doi.org/10.1248/CPB.38.2283
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1248/CPB.38.2283
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol	40467768	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1248/CPB.38.2283
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3-Ethenyl-3,7-dimethyloct-6-enoic acid	13128171	Click to see CC(=CCCC(C)(CC(=O)O)C=C)C	196.29	unknown	https://doi.org/10.1080/10412905.1993.9698256
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/J.PHYMED.2004.01.002
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/J.PHYMED.2004.01.002
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
> 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/10.1016/0031-9422(83)85052-3
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1080/10412905.1993.9698256
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
(+-)-Myrtenol	10582	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
(1S,3R,5S)-2(10)-Pinen-3-ol	12314318	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/J.PHYMED.2004.01.002
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Myrtenal	61130	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698256
Pinocarveol, (+-)-	102667	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698256
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3
Trans-alpha-Bergamotene	6429302	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698256
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
Carveol	7438	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Delta-Terpineol	81722	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	9991037	Click to see	220.35	unknown	https://doi.org/10.1248/CPB.38.2283
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1248/CPB.38.2283
beta Farnesene	15228937	Click to see	206.37	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Calamenene	6429077	Click to see	202.33	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Calamenene, trans-(+)-	6429022	Click to see	202.33	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1080/10412905.1993.9698256
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1993.9698256 https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1248/CPB.38.2283
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
gamma-Cadinene	6432404	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
trans-alpha-Bisabolene	24798703	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-alpha-Gurjunene	15560276	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698256
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol	5991	Click to see	296.40	unknown	https://doi.org/10.1080/10412905.1993.9698256
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool oxide (5-ring)	102611	Click to see	170.25	unknown	https://doi.org/10.1016/0031-9422(83)85052-3
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	https://doi.org/10.1016/0031-9422(83)85052-3 https://doi.org/10.1248/CPB.38.2283
Methylumbelliferone	10748	Click to see	176.17	unknown	https://doi.org/10.1248/CPB.38.2283 https://doi.org/10.1016/0031-9422(83)85052-3

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Lavandula latifolia

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