U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C12H20O2
Molecular Weight 196.286
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LINALYL ACETATE

SMILES

CC(=O)OC(C)(CCC=C(C)C)C=C

InChI

InChIKey=UWKAYLJWKGQEPM-UHFFFAOYSA-N
InChI=1S/C12H20O2/c1-6-12(5,14-11(4)13)9-7-8-10(2)3/h6,8H,1,7,9H2,2-5H3

HIDE SMILES / InChI

Molecular Formula C12H20O2
Molecular Weight 196.286
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
HPLC-FLD methods to quantify chloroaluminum phthalocyanine in nanoparticles, plasma and tissue: application in pharmacokinetic and biodistribution studies.
2011-08-25
Oil constituents of Artemisia nilagirica var. septentrionalis growing at different altitudes.
2010-12
Antibacterial effects of the essential oils of commonly consumed medicinal herbs using an in vitro model.
2010-10-27
Essential oil polymorphism of wild growing Hungarian thyme (Thymus pannonicus) populations in the Carpathian Basin.
2010-10
Acetylcholinesterase and butyrylcholinesterase inhibitory activity of Pinus species essential oils and their constituents.
2010-10
The influence of essential oils on human vigilance.
2010-09
Volatile fraction of lavender and bitter fennel infusion extracts.
2010-09
In vitro photo-induced cytotoxic activity of Citrus bergamia and C. medica L. cv. Diamante peel essential oils and identified active coumarins.
2010-09
In vitro synergistic efficacy of combination of amphotericin B with Myrtus communis essential oil against clinical isolates of Candida albicans.
2010-08
The study protocol of a blinded randomised-controlled cross-over trial of lavender oil as a treatment of behavioural symptoms in dementia.
2010-07-22
Volatile constituents of two rare subspecies of Thymus praecox.
2010-07
A DFT analysis of thermal decomposition reactions important to natural products.
2010-07
Selective removal of monoterpenes from bergamot oil by inclusion in deoxycholic acid.
2010-05-12
Variation of the chemical composition of essential oils in Tunisian populations of Thymus algeriensis Boiss. et Reut. (Lamiaceae) and implication for conservation.
2010-05
Investigation of the volatile fraction of rosemary infusion extracts.
2010-04-29
Responses of the Asian citrus psyllid to volatiles emitted by the flushing shoots of its rutaceous host plants.
2010-04
(R)-(-)-linalyl acetate and (S)-(-)-germacrene D from the leaves of Mexican Bursera linanoe.
2010-03
Branched-chain and aromatic amino acid catabolism into aroma volatiles in Cucumis melo L. fruit.
2010-02
Insecticidal activity of the essential oils from different plants against three stored-product insects.
2010
Comparative study of the chemical composition and antioxidant activity of six essential oils and their components.
2010
Suppression of linalool acetate production in Lavandula x intermedia.
2009-11
Chemical composition and antimicrobial activity of the essential oils from three chemotypes of Origanum vulgare L. ssp. hirtum (Link) Ietswaart growing wild in Campania (Southern Italy).
2009-07-27
Multiple component isolation in preparative multidimensional gas chromatography with characterisation by mass spectrometry and nuclear magnetic resonance spectroscopy.
2009-07-24
Fumigant insecticidal activity and repellent effect of five essential oils and seven monoterpenes on first-instar nymphs of Rhodnius prolixus.
2009-05
The antimicrobial activity of high-necrodane and other lavender oils on methicillin-sensitive and -resistant Staphylococcus aureus (MSSA and MRSA).
2009-03
Effect of needle damage on the release rate of Masson pine (Pinus massoniana) volatiles.
2009-03
High quality bergamot oil from Greece: Chemical analysis using chiral gas chromatography and larvicidal activity against the West Nile virus vector.
2009-02-18
Use of headspace mulberry paper bag micro solid phase extraction for characterization of volatile aromas of essential oils from Bulgarian rose and Provence lavender.
2009-01-05
Investigations on the effects of dietary essential oils and different husbandry conditions on the gut ecology in piglets after weaning.
2009
Intraplantar injection of bergamot essential oil into the mouse hindpaw: effects on capsaicin-induced nociceptive behaviors.
2009
Antifungal, phytotoxic and insecticidal properties of essential oil isolated from Turkish Origanum acutidens and its three components, carvacrol, thymol and p-cymene.
2008-12
Anti colon cancer components from Lebanese sage (Salvia libanotica) essential oil: Mechanistic basis.
2008-11
Enantioselective monoterpene alcohol acetylation in Origanum, Mentha and Salvia species.
2008-10
Lavender oil lacks natural protection against autoxidation, forming strong contact allergens on air exposure.
2008-09
Extraction and separation of volatile and fixed oils from berries of Laurus nobilis L. by Supercritical CO2.
2008-08-13
[Antimicrobial activity and GC-MS analysis of essential oil from lavender extracted by supercritical CO2 extraction and hydrodistillation].
2008-08
Essential oil of lavender inhibited the decreased attention during a long-term task in humans.
2008-07
Diversity of essential oil glands of clary sage (Salvia sclarea L., Lamiaceae).
2008-07
Antimutagenic and mutagenic activities of some terpenes in the bacterial reverse mutation assay.
2008-05-31
Poisoning by lavandin extract in a 18-month-old boy.
2008-04
Aroma constituents and alkylamides of red and green huajiao (Zanthoxylum bungeanum and Zanthoxylum schinifolium).
2008-03-12
Analysis of the volatile compounds of flowers and essential oils from Lavandula angustifolia cultivated in Northeastern Italy by headspace solid-phase microextraction coupled to gas chromatography-mass spectrometry.
2008-02
Autoxidation of linalyl acetate, the main component of lavender oil, creates potent contact allergens.
2008-01
Identification of a metagenome-derived esterase with high enantioselectivity in the kinetic resolution of arylaliphatic tertiary alcohols.
2007-10-21
Screening of antibacterial activities of twenty-one oxygenated monoterpenes.
2007-10-05
Screening of terpenes and derivatives for antimycobacterial activity; identification of geranylgeraniol and geranylgeranyl acetate as potent inhibitors of Mycobacterium tuberculosis in vitro.
2007-10
Further insights into the floral character of Touriga Nacional wines.
2007-08
Exploiting the yeast L-A viral capsid for the in vivo assembly of chimeric VLPs as platform in vaccine development and foreign protein expression.
2007-05-02
[Gas chromatography for analysis of essential oils. Characteristics of essential oil of Dracocephalum species and the influence of extraction method on its composition].
2007
Composition and antifungal activity of essential oils of Mentha piperita and Lavendula angustifolia on post-harvest phytopathogens.
2006
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:28:03 GMT 2025
Edited
by admin
on Mon Mar 31 19:28:03 GMT 2025
Record UNII
5K47SSQ51G
Record Status Validated (UNII)
Record Version
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Name Type Language
LINALYL ACETATE
FCC   FHFI   HSDB   INCI   MI  
INCI  
Official Name English
NSC-2138
Preferred Name English
LINALYL ACETATE [MI]
Common Name English
LINALYL ACETATE [HSDB]
Common Name English
LINALYL ACETATE [FHFI]
Common Name English
LINALOOL ACETATE, DL-
Common Name English
LINALYL ACETATE [FCC]
Common Name English
LINALYL ACETATE [USP-RS]
Common Name English
LINALOYL ACETATE, (±)-
Common Name English
FEMA NO. 2636
Code English
1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, ACETATE
Systematic Name English
LINALYL ACETATE, (±)-
Systematic Name English
BERGAMOL
Common Name English
Classification Tree Code System Code
EC SCIENTIFIC COMMITTEE ON CONSUMER SAFETY OPINION SCCS/1459/11
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
JECFA EVALUATION LINALYL ACETATE
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
Code System Code Type Description
SMS_ID
100000085822
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
RS_ITEM_NUM
1366578
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
PUBCHEM
8294
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
DAILYMED
5K47SSQ51G
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
JECFA MONOGRAPH
360
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
FDA UNII
5K47SSQ51G
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
RXCUI
1735331
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
MESH
C074463
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-116-4
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
EVMPD
SUB21632
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
HSDB
644
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
NSC
2138
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
WIKIPEDIA
LINALYL ACETATE
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
MERCK INDEX
m6821
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID7026946
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
CAS
115-95-7
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
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