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

Approval Year

PubMed

PubMed

TitleDatePubMed
Chromatographic (GC-MS, HPLC) and virological evaluations of Salvia sclarea infected by BBWV-I.
2001 Mar
Measurements by gas chromatography/pyrolysis/mass spectrometry: fundamental conditions in (2)H/(1)H isotope ratio analysis.
2002
Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils.
2002 Dec
Comparison of different extraction methods for the analysis of fragrances from Lavandula species by gas chromatography-mass spectrometry.
2002 Dec 20
Volatile components of peel and leaf oils of lemon and lime species.
2002 Feb 13
[Quality evaluation of essential oils].
2002 Mar
Composition and antifungal activity on soil-borne pathogens of the essential oil of Salvia sclarea from Greece.
2002 Nov 6
Antimicrobial activity of essential oils isolated from Portuguese endemic species of Thymus.
2003
Fragrance material review on linalyl acetate.
2003 Jul
Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage.
2003 Jul 2
A molecular mechanism of enantiorecognition of tertiary alcohols by carboxylesterases.
2003 Jun 6
Evaluation of gliadins nanoparticles as drug delivery systems: a study of three different drugs.
2003 Mar 6
Comparative analysis of the oil and supercritical CO2 extract of Elettaria cardamomum (L.) Maton.
2004 Oct 6
Headspace solid-phase microextraction-gas chromatography--mass spectrometry analysis of the volatile compounds of Evodia species fruits.
2005 Sep 16
Composition and antifungal activity of essential oils of Mentha piperita and Lavendula angustifolia on post-harvest phytopathogens.
2006
Aqueous solubility of liquid monoterpenes at 293 K and relationship with calculated log P value.
2006 Apr
Anticonflict effects of lavender oil and identification of its active constituents.
2006 Dec
Cleaning products and air fresheners: emissions and resulting concentrations of glycol ethers and terpenoids.
2006 Jun
A new phthalic acid ester from Ajuga bracteosa.
2006 May 20
Female-biased attraction of Oriental fruit fly, bactrocera dorsalis (Hendel), to a blend of host fruit volatiles from Terminalia catappa L.
2006 Nov
Further insights into the floral character of Touriga Nacional wines.
2007 Aug
Odour fingerprint acquisition by means of comprehensive two-dimensional gas chromatography-olfactometry and comprehensive two-dimensional gas chromatography/mass spectrometry.
2007 Feb 9
Screening of antibacterial activities of twenty-one oxygenated monoterpenes.
2007 Jul-Aug
Screening of terpenes and derivatives for antimycobacterial activity; identification of geranylgeraniol and geranylgeranyl acetate as potent inhibitors of Mycobacterium tuberculosis in vitro.
2007 Oct
Antimutagenic and mutagenic activities of some terpenes in the bacterial reverse mutation assay.
2008 May 31
Anti colon cancer components from Lebanese sage (Salvia libanotica) essential oil: Mechanistic basis.
2008 Nov
Enantioselective monoterpene alcohol acetylation in Origanum, Mentha and Salvia species.
2008 Oct
Multiple component isolation in preparative multidimensional gas chromatography with characterisation by mass spectrometry and nuclear magnetic resonance spectroscopy.
2009 Jul 24
Fumigant insecticidal activity and repellent effect of five essential oils and seven monoterpenes on first-instar nymphs of Rhodnius prolixus.
2009 May
Suppression of linalool acetate production in Lavandula x intermedia.
2009 Nov
Insecticidal activity of the essential oils from different plants against three stored-product insects.
2010
In vitro synergistic efficacy of combination of amphotericin B with Myrtus communis essential oil against clinical isolates of Candida albicans.
2010 Aug
A DFT analysis of thermal decomposition reactions important to natural products.
2010 Jul
Investigation of the volatile fraction of rosemary infusion extracts.
2010 Jul-Sep
The influence of essential oils on human vigilance.
2010 Sep
Patents
Name Type Language
LINALYL ACETATE
FCC   FHFI   HSDB   INCI   MI  
INCI  
Official Name English
LINALYL ACETATE [MI]
Common Name English
LINALYL ACETATE [HSDB]
Common Name English
LINALYL ACETATE [FHFI]
Common Name English
LINALYL ACETATE [INCI]
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
NSC-2138
Code English
Classification Tree Code System Code
EC SCIENTIFIC COMMITTEE ON CONSUMER SAFETY OPINION SCCS/1459/11
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
JECFA EVALUATION LINALYL ACETATE
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
Code System Code Type Description
SMS_ID
100000085822
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
RS_ITEM_NUM
1366578
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
PUBCHEM
8294
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
DAILYMED
5K47SSQ51G
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
JECFA MONOGRAPH
360
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
FDA UNII
5K47SSQ51G
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
RXCUI
1735331
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
MESH
C074463
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-116-4
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
EVMPD
SUB21632
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
HSDB
644
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
NSC
2138
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
WIKIPEDIA
LINALYL ACETATE
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
MERCK INDEX
m6821
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID7026946
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY
CAS
115-95-7
Created by admin on Fri Dec 15 18:57:44 GMT 2023 , Edited by admin on Fri Dec 15 18:57:44 GMT 2023
PRIMARY