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
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

Suggest a correction or add new data!

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	80.0x	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

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

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

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

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

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

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

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

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

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

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 / Toluenes
1-Ethyl-2-methylbenzene	11903	Click to see CCC1=CC=CC=C1C	120.19	unknown	https://doi.org/10.1007/S10600-009-9210-8
> Benzenoids / Phenols / Methoxyphenols
Maesol	128958	Click to see CC1=C(C=C(C=C1OC)CCCCCCCCCCCCC2=CC(=C(C(=C2)OC)C)O)O	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 CCCCCCCCCCCCCC	198.39	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	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 CCCCCCOC(=O)CCC	172.26	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
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 CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727
Oct-3-EN-1-YL acetate	50607	Click to see CCCCC=CCCOC(=O)C	170.25	unknown	https://doi.org/10.1080/10412905.1997.9700727
Octyl Acetate	8164	Click to see CCCCCCCCOC(=O)C	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
(3R)-oct-1-en-3-ol	6992244	Click to see CCCCCC(C=C)O	128.21	unknown	https://doi.org/10.1007/S10600-009-9210-8
1-Octen-3-Ol	18827	Click to see CCCCCC(C=C)O	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
[(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-octadien-1-ol	4458	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8
5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol acetate	14268092	Click to see CC(=CCC(COC(=O)C)C(=C)C)C	196.29	unknown	https://doi.org/10.1007/S10600-009-9210-8
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	https://doi.org/10.1080/10412905.1997.9700727
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	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 CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1021/JF9708296
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
Lavandulol	5464156	Click to see CC(=CCC(CO)C(=C)C)C	154.25	unknown	https://doi.org/10.1021/JF9708296
Lavandulyl acetate, (+/-)-	30247	Click to see CC(=CCC(COC(=O)C)C(=C)C)C	196.29	unknown	https://doi.org/10.1007/S10600-009-9210-8
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1007/S10600-009-9210-8
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	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
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1021/JF9708296
Linalyl propionate	61098	Click to see CCC(=O)OC(C)(CCC=C(C)C)C=C	210.31	unknown	https://doi.org/10.1080/10412905.1997.9700727
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	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
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1080/10412905.1997.9700727
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	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 CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	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
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol	12314318	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	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
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
alpha-Bergamotene, (E)-(-)-	6429302	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727 https://doi.org/10.1016/S0031-9422(00)80692-5
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1997.9700727
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	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 CC1(C2CCC1(C(=O)C2)C)C	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 CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
> 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/10.1021/JF049033E https://doi.org/10.1021/JF9708296 https://doi.org/10.1080/10412905.1997.9700727
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF9708296 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
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1997.9700727
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/S10600-009-9210-8
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 CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
(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
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	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
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)-	26318	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/S10600-009-9210-8
Cadalene	10225	Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C	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 epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	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 CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	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
trans-Nerolidol	5284507	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1997.9700727
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
1,7-di-epi-alpha-Cedrene	10878276	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1997.9700727
alpha-Cederene	442348	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	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 CCCCCC(C=C)OC(=O)C	170.25	unknown	https://doi.org/10.1080/10412905.1997.9700727
Hexyl Acetate	8908	Click to see CCCCCCOC(=O)C	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 CC(C)C(=O)O	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
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	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 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
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 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
Nepetoidin B	5316819	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
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin	10748	Click to see COC1=CC2=C(C=C1)C=CC(=O)O2	176.17	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
7-Methoxy-5-hydroxy-4-(4-hydroxyphenyl)chroman-2-one	53821997	Click to see COC1=CC(=C2C(CC(=O)OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/S0031-9422(00)80692-5

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Lavandula angustifolia

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