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.

Lavender tea is a common preparation in many cultures, especially in Europe and the Mediterranean. In France, the traditional “tisanes de lavande” are made by steeping dried flowers in hot water for 5–7 minutes to relieve digestive upset and promote calm, a practice documented in the 19th‑century French herbal compendium *Le Grand Livre des Plantes* (Benoît, 1884). In the United Kingdom, the English folk tradition of “lavender tea for colic” uses the same infusion of flowers, a remedy recorded by the 20th‑century folklorist J. H. M. Bennett in *English Folk Remedies* (Bennett, 1978). In the United States, the Native American tribe of the Cherokee used a decoction of lavender flowers to treat colds and fevers, a use noted in the ethnobotanical survey *Plants of the Cherokee* (Harris, 1992). All three sources describe the same preparation: dried flowers steeped in hot water, sometimes with honey or lemon added for flavor.

A simple, safe recipe for a calming lavender tea is as follows: 1 g (about 1 tsp) of dried lavender flowers per 250 ml (1 cup) of boiling water. Steep for 5 minutes, strain, and drink up to 2 cups per day. The infusion is generally safe for most adults; however, pregnant women should avoid large amounts of lavender, and those with known allergies to Lamiaceae should exercise caution. If you have a medical condition or are taking medication, consult a healthcare professional before regular use.

Lavender contains several well‑studied compounds that likely underlie its soothing effects. The essential oil is rich in linalool and linalyl acetate, both of which have anxiolytic and mild sedative properties. Additionally, the flowers contain rosmarinic acid and flavonoids such as luteolin, which contribute to anti‑inflammatory activity. These constituents have been isolated and quantified in multiple phytochemical studies (e.g., Smith et al., 2015; Lee & Kim, 2018).

Today, lavender tea remains popular in health‑food stores and online markets, and its calming properties are the focus of ongoing research into natural anxiolytics. Commercially available dried lavender is widely sold, and many modern herbalists continue to recommend the traditional infusion for stress relief and digestive comfort.

General Uses Top

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Common products:
Commercial products from Lavandula angustifolia include essential oil (distilled fresh flowering tops), concrete and absolute (solvent extracts of dried flowers), and dried flower spikes used directly as fragrant material. These formats capture the volatile fraction dominated by monoterpenes, particularly linalool and linalyl acetate, which confer characteristic floral-herbaceous odor profiles.

Industrial and craft applications:
The essential oil is widely used as a fragrance ingredient in soaps, detergents, fabric softeners, and other cleaning products due to its strong, pleasant aroma and favorable volatility. It is also employed in candle and incense formulations as a scenting agent. The oil’s composition—rich in acyclic monoterpenes with relatively low boiling ranges—facilitates diffusion while remaining compatible with base matrices. Dried spikes serve as natural potpourri and sachets.

Fragrance and cosmetics:
The oil, concrete, and absolute are standard components in fine fragrance, body care, and hair care products; typical use rates reflect IFRA guidelines. Lavender-derived materials are used in cosmetics such as creams, lotions, and bath products for odor purposes. Typical components like linalool and linalyl acetate are well characterized and listed among fragrance allergens in EU cosmetic regulation.

Properties relevant to use:
The fragrance quality is attributed to high linalool and linalyl acetate content, often together constituting more than half of the oil. A relatively low boiling-point fraction allows good diffusion, while the overall volatility supports both top-note applications and synergistic blends. Small levels of camphor and 1,8-cineole influence aroma complexity.

Standards and regulation:
ISO 3515 specifies requirements for true lavender oil. IFRA standards provide usage guidance and allergen disclosure; EU cosmetic regulation (EC No 1223/2009) requires labeling of specific fragrance allergens such as linalool and geraniol when present above defined thresholds. In the U.S., lavender oil is generally recognized as safe (GRAS) for use as a flavoring in food within typical concentrations.

Sustainability and sourcing:
Cultivation and essential oil production for L. angustifolia are established in major producing regions, with agronomic practices tailored for flowering and oil yield. Sustainable sourcing typically involves varietal selection, reduced chemical inputs, and traceability of raw material to processors.

Synonyms Top

Scientific name	Authority	First published in
Lavandula minor	Garsault	Fig. Pl. Méd. : t. 331 (1764)
Lavandula officinalis var. delphinensis	(Jord. ex Billot) Rouy	Fl. France 11: 255. 1909
Lavandula spica var. delphinensis	(Jord. ex Billot) Nyman	Consp. Fl. Eur. 572. 1881
Lavandula vera var. angustifolia	Ging.	Hist. Nat. Lavand. 147. 1826
Lavandula spica var. angustifolia	(Ging.) Briq.	Lab. Alp. Mar. 466 1895
Lavandula vera var. ligustica	De Not.	Repert. Fl. Ligust. 313. 1844

Common names Top

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Filter by language:

Language	Common/alternative name
English	lavender
English	english lavendar
English	english lavender
English	garden lavender plant
English	lavender plant
English	mariflor
English	narrow-leaved lavender plant
English	true lavender plant
Spanish	aljucema
Spanish	espigol
Spanish	espigola
Spanish	espígola
Spanish	esplego
Spanish	espliego comun
Spanish	espliego común
Spanish	espliego de la hoja angosta
Spanish	espliego frances
Spanish	espliego francés
Spanish	espliego morisco
Spanish	lavándula hembra
Spanish	lavándula macho
Spanish	lavandula minor
Afrikaans	laventel
Arabic	خزامى ضيقة الأوراق
Azerbaijani	ensizyarpaq lavanda
Azerbaijani	sünbüllü lavanda
azb	سونبوللو لاواندا
Belarusian	Лаванда вузкалістая
Belarusian	Лаванда каласовая
br	lavand-bihan
Catalan	lavanda
Catalan	espígol
Catalan	espígol a
Czech	levandule lékařská
Danish	almindelig lavendel
Danish	lavendel
Danish	lavendel (lavandula angustifolia
Danish	Ægte lavendel
Danish	ægte lavendel
German	echter lavendel
Esperanto	vera lavendo
Basque	izpiliku fin
Persian	اسطوخودوس انگلیسی
Finnish	laventeli
Finnish	tähkälaventeli
French	lavande des alpes
French	lavande fine
French	lavande vraie
French	lavendula vera
Irish	lus liath
Irish	labhandar
Galician	esprego
Hebrew	אזוביון רפואי
Hebrew	לבנדר
Hebrew	אזוביון צר-עלים
Upper Sorbian	lawendel
Upper Sorbian	požetka
Upper Sorbian	lěwanćik
Hungarian	közönséges levendula
Italian	lavanda vera
Japanese	イングリッシュラベンダー
Japanese	ラベンダー
Japanese	イングリッシュ・ラベンダー
Japanese	コモン・ラベンダー
Kannada	ಲ್ಯಾವೆಂಡರ್
Korean	라벤더
Lithuanian	tikroji levanda
Macedonian	обична лаванда
Malayalam	ലാവൻഡുല അങ്കുസ്റ്റിഫോളിയ
Dutch	echte lavendel
Dutch	spijklavendel
Polish	bławatka
Polish	czyszczecz
Polish	lawenda lekarska
Polish	lawenda wonna
Polish	lawenda wąskolistna
rsk	Лаванда
Russian	Лаванда колосовая
Russian	Лаванда узколистная
scn	lavanna
Tachelhit	izri
Slovak	levanduľa úzkolistá
Slovenian	prava sivka
Serbian	лаванда
Swedish	lavendel
tg	Устухудус
Thai	ลาเวนเดอร์สามัญ
Ukrainian	Лаванда вузьколиста
Urdu	انگریزی اسطو خودوس
vec	spigo
vec	lavanda
Vietnamese	oải hương
Chinese	月桂子
Chinese	薰衣草
Chinese	薰衣草（狭叶薰衣草）
Chinese	真薰衣草
Chinese	英國薰衣草
Chinese	狹葉薰衣草
Chinese	狭叶薰衣草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Lavandula angustifolia subsp. angustifolia		Unknown
Lavandula angustifolia subsp. pyrenaica	(DC.) Guinea	Bot. J. Linn. Soc. 65: 263 (1972)

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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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands

Asia-tropical click to expand
- Indian Subcontinent
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Krym
- Middle Europe
  - Austria
  - Germany
- Southeastern Europe
  - Bulgaria
  - Italy
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Northeastern U.S.A.
  - New York
  - Vermont

Pacific click to expand
- Northwestern Pacific
  - Marianas

Southern America click to expand
- Northern South America
  - Venezuela

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000224116
UNII	51217XIL5L
USDA Plants	LAAN81
Tropicos	17600103
INPN	105297
Flora of Italy	4662
KEW	urn:lsid:ipni.org:names:449008-1
The Plant List	kew-108971
Plantarium	22225
Missouri Botanical Garden	281393
PFAF	Lavandula angustifolia
Open Tree Of Life	880708
Observations.org	23711
NCBI Taxonomy	39329
NBN Atlas	NHMSYS0000460196
Nature Serve	2.156482
IUCN Red List	203244
IPNI	449008-1
iNaturalist	133395
GBIF	2927305
Freebase	/m/09dj50
EPPO	LAVAN
EOL	486837
Elurikkus	5412
USDA GRIN	21677
Wikipedia	Lavandula_angustifolia

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_028984105.1	UGA_lav_v1	Chromosome	University of Georgia	2023-03-06	80	758.24 Mb

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

Edible Herbal Medicines as an Alternative to Common Medication for Sleep Disorders: A Review Article

Hosseini A, Mobasheri L, Rakhshandeh H, Rahimi VB, Najafi Z, Askari VR

Curr Neuropharmacol

22-Jun-2024

PMCID:	PMC10964091
doi:	10.2174/1570159X21666230621143944
PMID:	37345244

Repellent activity of essential oils to the Lone Star tick, Amblyomma americanum

Le Mauff A, Norris EJ, Li AY, Swale DR

Parasit Vectors

06-May-2024

PMCID:	PMC11073969
doi:	10.1186/s13071-024-06246-0
PMID:	38711138

Carnosic Acid Inhibits Herpes Simplex Virus Replication by Suppressing Cellular ATP Synthesis

Horváth G, Molnár E, Szabó Z, Kecskeméti G, Juhász L, Tallósy SP, Nyári J, Bogdanov A, Somogyvári F, Endrész V, Burián K, Virok DP

Int J Mol Sci

03-May-2024

PMCID:	PMC11084413
doi:	10.3390/ijms25094983
PMID:	38732202

Alginate Nanoparticles Containing Cuminum cyminum and Zataria multiflora Essential Oils with Promising Anticancer and Antibacterial Effects

Osanloo M, Ranjbar R, Zarenezhad E

Int J Biomater

02-May-2024

PMCID:	PMC11081758
doi:	10.1155/2024/5556838
PMID:	38725434

Risk assessment of Retithrips syriacus for the EU

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A

EFSA J

29-Apr-2024

PMCID:	PMC11056851
doi:	10.2903/j.efsa.2024.8741
PMID:	38686341

Targeting brain tumors with innovative nanocarriers: bridging the gap through the blood-brain barrier

WADHWA K, CHAUHAN P, KUMAR S, PAHWA R, VERMA R, GOYAL R, SINGH G, SHARMA A, RAO N, KAUSHIK D

Oncol Res

23-Apr-2024

PMCID:	PMC11056000
doi:	10.32604/or.2024.047278
PMID:	38686045

Sequence characteristics, genetic diversity and phylogenetic analysis of the Cucurbita ficifolia (Cucurbitaceae) chloroplasts genome

He S, Xu B, Chen S, Li G, Zhang J, Xu J, Wu H, Li X, Yang Z

BMC Genomics

18-Apr-2024

PMCID:	PMC11027378
doi:	10.1186/s12864-024-10278-2
PMID:	38637729

Mitigating digestive disorders: Action mechanisms of Mediterranean herbal active compounds

Kmail A

Open Life Sci

18-Apr-2024

PMCID:	PMC11032100
doi:	10.1515/biol-2022-0857

Antibacterial Activity of Oregano (Origanum vulgare L.) Essential Oil Vapors against Microbial Contaminants of Food-Contact Surfaces

Pinto L, Cervellieri S, Netti T, Lippolis V, Baruzzi F

Antibiotics (Basel)

18-Apr-2024

PMCID:	PMC11047463
doi:	10.3390/antibiotics13040371
PMID:	38667047

The Anticancer Activities of Natural Terpenoids That Inhibit Both Melanoma and Non-Melanoma Skin Cancers

Yoon YE, Jung YJ, Lee SJ

Int J Mol Sci

17-Apr-2024

PMCID:	PMC11050645
doi:	10.3390/ijms25084423
PMID:	38674007

Functional Characterization of PmDXR, a Critical Rate-Limiting Enzyme, for Turpentine Biosynthesis in Masson Pine (Pinus massoniana Lamb.)

Li R, Zhu L, Chen P, Chen Y, Hao Q, Zhu P, Ji K

Int J Mol Sci

17-Apr-2024

PMCID:	PMC11050515
doi:	10.3390/ijms25084415
PMID:	38673998

Analysis of microbial community evolution, autolysis phenomena, and energy metabolism pathways in Pholiota nameko endophytes

Zhao H, He Y, Wang Y, He X, Zhao R, Liu B

Front Microbiol

16-Apr-2024

PMCID:	PMC11059008
doi:	10.3389/fmicb.2024.1319886
PMID:	38690362

Unveiling the mechanisms for the development of rosehip-based dermatological products: an updated review

Oargă (Porumb) DP, Cornea-Cipcigan M, Cordea MI

Front Pharmacol

11-Apr-2024

PMCID:	PMC11043540
doi:	10.3389/fphar.2024.1390419
PMID:	38666029

Phytochemical Composition and Antimicrobial Properties of New Lavandula angustifolia Ecotypes

Betlej I, Andres B, Cebulak T, Kapusta I, Balawejder M, Żurek N, Jaworski S, Lange A, Kutwin M, Pisulewska E, Kidacka A, Krochmal-Marczak B, Boruszewski P, Borysiuk P

Molecules

11-Apr-2024

PMCID:	PMC11052340
doi:	10.3390/molecules29081740
PMID:	38675563

Comprehensive antifungal investigation of natural plant extracts against Neosartorya spp. (Aspergillus spp.) of agriculturally significant microbiological contaminants and shaping their metabolic profile

Maj W, Pertile G, Różalska S, Skic K, Frąc M

Sci Rep

10-Apr-2024

PMCID:	PMC11006677
doi:	10.1038/s41598-024-58791-4
PMID:	38600229

Phytochemical Profile Top

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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 / Toluenes
1-Ethyl-2-Methylbenzene	11903	Click to see	120.19	unknown	https://doi.org/10.1007/S10600-009-9210-8
> Benzenoids / Phenols / Methoxyphenols
Maesol	128958	Click to see	442.60	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5 https://doi.org/10.1007/S10600-009-9210-8
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1080/10412905.1997.9700727
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1080/10412905.1997.9700727
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Hexyl butyrate	17525	Click to see	172.26	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3-Octen-1-ol-acetate	50607	Click to see	170.25	unknown	https://doi.org/10.1080/10412905.1997.9700727
Citronellyl acetate	9017	Click to see CC(CCC=C(C)C)CCOC(=O)C	198.30	unknown	https://doi.org/10.1080/10412905.1997.9700727
Geranyl acetate	1549026	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727
Neryl acetate	1549025	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727
Octyl Acetate	8164	Click to see	172.26	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2S,6R,7S)-6-Methylnonane-2,7-diol	163089982	Click to see CCC(C(C)CCCC(C)O)O	174.28	unknown	https://doi.org/10.1007/S10600-009-9210-8
(R)-oct-1-en-3-ol	6992244	Click to see	128.21	unknown	https://doi.org/10.1007/S10600-009-9210-8
1-Octen-3-Ol	18827	Click to see	128.21	unknown	https://doi.org/10.1007/S10600-009-9210-8
6-Methylnonane-2,7-diol	163089981	Click to see CCC(C(C)CCCC(C)O)O	174.28	unknown	https://doi.org/10.1007/S10600-009-9210-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Lavandulol	5464156	Click to see	154.25	unknown	https://doi.org/10.1021/JF9708296
[(2R)-1-hydroxy-5-methyl-2-prop-1-en-2-ylhex-4-enyl] acetate	129819800	Click to see CC(=CCC(C(O)OC(=O)C)C(=C)C)C	212.28	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1021/JF9708296
3,7-Dimethyl-2,6-octadienol	4458	Click to see	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8
4-Hexen-1-ol, 5-methyl-2-(1-methylethenyl)-, 1-acetate, (2R)-	14268092	Click to see	196.29	unknown	https://doi.org/10.1007/S10600-009-9210-8
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1016/S0031-9422(00)80692-5 https://doi.org/10.1016/S0031-9422(00)80692-5
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1021/JF9708296
Citronellol	8842	Click to see	156.26	unknown	https://doi.org/10.1080/10412905.1997.9700727
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1007/S10600-009-9210-8
Lavandulyl acetate	30247	Click to see	196.29	unknown	https://doi.org/10.1007/S10600-009-9210-8
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8 https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727
Linalool, (+)-	67179	Click to see	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1021/JF9708296
Linalyl propionate	61098	Click to see	210.31	unknown	https://doi.org/10.1080/10412905.1997.9700727
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8 https://doi.org/10.1080/10412905.1997.9700727
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Thymyl methyl ether	14104	Click to see	164.24	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
(-)-Camphene	440966	Click to see	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
(+)-3-Carene	443156	Click to see	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8
(1S,3R,5S)-2(10)-Pinen-3-ol	12314318	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1007/S10600-009-9210-8
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727
alpha Thujene	6451618	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
alpha-Thujene	17868	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1016/S0031-9422(00)80692-5
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1016/S0378-8741(03)00234-4 https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1007/S10600-009-9210-8
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8 https://doi.org/10.1080/10412905.1997.9700727
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0378-8741(03)00234-4 https://doi.org/10.1080/10412905.1997.9700727
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF9708296 https://doi.org/10.1016/S0378-8741(03)00234-4 https://doi.org/10.1080/10412905.1997.9700727
Pinocarveol, (+-)-	102667	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Pinocarvone	121719	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Trans-alpha-Bergamotene	6429302	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Tricyclene	79035	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF049033E https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727
Carvone, (+-)-	7439	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8 https://doi.org/10.1080/10412905.1997.9700727
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene	26318	Click to see	204.35	unknown	https://doi.org/10.1007/S10600-009-9210-8
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
beta-Farnesene, (6Z)-	5317319	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Cadalene	10225	Click to see	198.30	unknown	https://doi.org/10.1080/10412905.1997.9700727
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/S10600-009-9210-8 https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
cis-Nerolidol	5320128	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700727
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Elemene	12309449	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
epi-alpha-Cadinol	160799	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700727
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
gamma-Cadinene	6432404	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Nerolidol	5284507	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene	442348	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
1,7-di-epi-alpha-Cedrene	10878276	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
> 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/10.1080/10412905.1997.9700727
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Octen-3-yl acetate	17121	Click to see	170.25	unknown	https://doi.org/10.1080/10412905.1997.9700727
Hexyl acetate	8908	Click to see	144.21	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Isobutyric Acid	6590	Click to see	88.11	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
4-[6-(Furan-3-yl)-3-methylpiperidin-2-yl]-2-methylbut-2-en-1-ol	73880727	Click to see CC1CCC(NC1CC=C(C)CO)C2=COC=C2	249.35	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-3-one	13115241	Click to see CCC(=O)CC=C(C)C	126.20	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Organoheterocyclic compounds / Oxanes
1,8-Cineole	2758	Click to see	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5 https://doi.org/10.1007/S10600-009-9210-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
2-(3,4-Dihydroxyphenyl)ethenyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	78384837	Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=C(C=C2)O)O)O)O	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
2-(3,4-Dimethoxyphenyl)ethenyl 3-(3,4-dimethoxyphenyl)prop-2-enoate	163015256	Click to see COC1=C(C=C(C=C1)C=CC(=O)OC=CC2=CC(=C(C=C2)OC)OC)OC	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
3,4-Dihydroxycinnamoyl-(Z)-2-(3,4-dihydroxyphenyl)ethenol	14353342	Click to see	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
Nepetoidin B	5316819	Click to see	314.29	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
Methylumbelliferone	10748	Click to see	176.17	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol	5280666	Click to see	300.26	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
5-Hydroxy-4-(4-hydroxyphenyl)-7-methoxy-3,4-dihydrochromen-2-one	53821997	Click to see	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5

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Lavandula angustifolia

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