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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14O
Molecular Weight 150.2176
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARVACROL

SMILES

CC(C)C1=CC(O)=C(C)C=C1

InChI

InChIKey=RECUKUPTGUEGMW-UHFFFAOYSA-N
InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H14O
Molecular Weight 150.2176
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antitussive effect of Carum copticum in guinea pigs.
2005-02-10
Composition and antibacterial activity of essential oil of Lantana achyranthifolia Desf. (Verbenaceae).
2005-01-15
Chemical compositions and antibacterial effects of essential oils of Turkish oregano (Origanum minutiflorum), bay laurel (Laurus nobilis), Spanish lavender (Lavandula stoechas L.), and fennel (Foeniculum vulgare) on common foodborne pathogens.
2004-12-29
Biological significance of essential oil of Zataria multiflora boiss.
2004-12
Constituents of aromatic plants: carvacrol.
2004-12
[Determination of carvacrol and thymol in Mosla chinensis by HPLC].
2004-11
Effect of plant extracts and formic acid on the intestinal equilibrium of early-weaned pigs.
2004-11
Evaluation of carvacrol and eugenol as prophylaxis and treatment of vaginal candidiasis in an immunosuppressed rat model.
2004-11
Determination of isopropylmethylphenols in black seed oil by differential pulse voltammetry.
2004-10-29
Seasonal, populational and ontogenic variation in the volatile oil content and composition of individuals of Origanum vulgare subsp. Hirtum, assessed by GC headspace analysis and by SPME sampling of individual oil glands.
2004-10-29
Antibacterial activities of plant essential oils and their components against Escherichia coli O157:H7 and Salmonella enterica in apple juice.
2004-09-22
Radical rebound mechanism in cytochrome P-450-catalyzed hydroxylation of the multifaceted radical clocks alpha- and beta-thujone.
2004-09-17
Alpha- and beta-thujone radical rearrangements and isomerizations. A new radical clock.
2004-08-20
Thymol and carvacrol binding to DNA: model for drug-DNA interaction.
2004-08-05
Essential oils: their antibacterial properties and potential applications in foods--a review.
2004-08-01
Antibacterial activities of naturally occurring compounds against antibiotic-resistant Bacillus cereus vegetative cells and spores, Escherichia coli, and Staphylococcus aureus.
2004-08
Use of carvacrol and cymene to control growth and viability of Listeria monocytogenes cells and predictions of survivors using frequency distribution functions.
2004-07
Chemical composition and antimicrobial activity of the essential oils from the gum of Turkish pistachio (Pistacia vera L.).
2004-06-16
In vitro antioxidant, antimicrobial, and antiviral activities of the essential oil and various extracts from herbal parts and callus cultures of Origanum acutidens.
2004-06-02
Antifungal treatment with carvacrol and eugenol of oral candidiasis in immunosuppressed rats.
2004-06
Chemical composition and antifungal activity of the essential oil of Thymbra capitata.
2004-06
Radiosensitization of Escherichia coli and Salmonella Typhi in ground beef.
2004-06
Chemical composition and extraction yield of the extract of Origanum vulgare obtained from sub- and supercritical CO2.
2004-05-19
Isopanduratin A from Kaempferia pandurata as an active antibacterial agent against cariogenic Streptococcus mutans.
2004-04
Analysis of essential oil of Satureja thymbra by hydrodistillation, thermal desorber, and headspace GC/MS techniques and its antimicrobial activity.
2004-04
Composition and the in vitro antimicrobial activities of the essential oils of some Thymus species.
2004-03-17
Immunostimulatory effect of dietary oregano etheric oils on lymphocytes from growth-retarded, low-weight growing-finishing pigs and productivity.
2004-03-15
In vitro antimicrobial and antioxidant activities of the essential oils and various extracts of Thymus eigii M. Zohary et P.H. Davis.
2004-03-10
Effects of terpenoid phenol derivatives on calcium current in canine and human ventricular cardiomyocytes.
2004-03-08
[Oregano: properties, composition and biological activity].
2004-03
Inhibition of Bacillus subtilis and Listeria innocua by nisin in combination with some naturally occurring organic compounds.
2004-03
Susceptibility of methicillin-resistant staphylococci to oregano essential oil, carvacrol and thymol.
2004-01-30
Investigation of the Origanum onites L. essential oil using the chorioallantoic membrane (CAM) assay.
2004-01-28
Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae.
2004-01
Antifungal activity of Thymus oils and their major compounds.
2004-01
Plant oils thymol and eugenol affect cattle and swine waste emissions differently.
2004
Content and composition of the essential oil of Thymus serpyllum L. growing wild in Estonia.
2004
Mode of antimicrobial action of vanillin against Escherichia coli, Lactobacillus plantarum and Listeria innocua.
2004
Influence of nitrogen fertilizers on the yield and composition of thyme (Thymus vulgaris).
2003-12-17
Quantitative analytical traceability of phytogenic active principles.
2003-12
Effect of the volatile constituents isolated from Thymus albicans, Th. mastichina, Th. carnosus and Thymbra capitata in sunflower oil.
2003-12
Relaxant effects of different fractions of essential oil from Carum copticum on guinea pig tracheal chains.
2003-12
Screening chemical composition and in vitro antioxidant and antimicrobial activities of the essential oils from Origanum syriacum L. growing in Turkey.
2003-12
LC-UV-solid-phase extraction-NMR-MS combined with a cryogenic flow probe and its application to the identification of compounds present in Greek oregano.
2003-11-15
Chemical composition and antifungal activity of essential oils of seven Moroccan Labiatae against Botrytis cinerea Pers: Fr.
2003-11
Analysis of essential oil of Coridothymus capitatus (L.) and its antibacterial and antifungal activity.
2003-10-28
Essential oils from Mediterranean lamiaceae as weed germination inhibitors.
2003-10-08
Chemical composition and antifungal activity of the essential oil of Origanum virens on Candida species.
2003-09
Relaxant effects of carvacrol on guinea pig tracheal chains and its possible mechanisms.
2003-09
Activity of natural antimicrobial compounds against Escherichia coli and Salmonella enterica serovar Typhimurium.
2003
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:53:13 GMT 2025
Edited
by admin
on Mon Mar 31 17:53:13 GMT 2025
Record UNII
9B1J4V995Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARVACROL
FCC   FHFI   HSDB   INCI   MI   WHO-DD  
INCI  
Official Name English
NSC-6188
Preferred Name English
CARVACROL [FHFI]
Common Name English
2-P-CYMENOL
Common Name English
ISOPROPYL-O-CRESOL
Common Name English
Carvacrol [WHO-DD]
Common Name English
CARVACROL [MI]
Common Name English
ISOTHYMOL
Common Name English
FEMA NO. 2245
Code English
ANTIOXINE
Common Name English
DENTOL
Common Name English
CARVACROL [HSDB]
Common Name English
CARVACROL [FCC]
Common Name English
5-ISOPROPYL-2-METHYLPHENOL
Systematic Name English
2-METHYL-5-(1-METHYLETHYL)PHENOL
Systematic Name English
2-HYDROXY-P-CYMENE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
EPA PESTICIDE CODE 22104
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
NCI_THESAURUS C737
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
DSLD 2480 (Number of products:21)
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
JECFA EVALUATION CARVACROL
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
Code System Code Type Description
DAILYMED
9B1J4V995Q
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
MESH
C073316
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
NSC
6188
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-889-6
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID6042074
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
MERCK INDEX
m3142
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY Merck Index
SMS_ID
100000092827
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
EVMPD
SUB29258
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
ALANWOOD
carvacrol
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
FDA UNII
9B1J4V995Q
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
PUBCHEM
10364
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
HSDB
906
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
CHEBI
3440
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
NCI_THESAURUS
C83602
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
RXCUI
1998840
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
CAS
499-75-2
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
WIKIPEDIA
CARVACROL
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
JECFA MONOGRAPH
589
Created by admin on Mon Mar 31 17:53:13 GMT 2025 , Edited by admin on Mon Mar 31 17:53:13 GMT 2025
PRIMARY
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Compound measured as 10.80% of the composition of the steam distillate of Elymus repens rhizome as per R Boesel in Planta Medica iss:4 pg:399-400, 1989.
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