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

Details

Stereochemistry ACHIRAL
Molecular Formula C10H14
Molecular Weight 134.2182
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CYMENE

SMILES

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

InChI

InChIKey=HFPZCAJZSCWRBC-UHFFFAOYSA-N
InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H14
Molecular Weight 134.2182
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Occurrence of organic pollutants in recovered soil fines from construction and demolition waste.
2001
[Chemical constituents in volatile oil from fruits of Alpinia oxyphylla Miq].
2001 Apr
Identification of volatile constituents of Tambourissa leptophylla.
2001 Apr
Biotransformations catalyzed by cloned p-cymene monooxygenase from Pseudomonas putida F1.
2001 Apr
Self-assembled organometallic [12]metallacrown-3 complexes.
2001 Aug 3
Bioconversion of limonene to increased concentrations of perillic acid by Pseudomonas putida GS1 in a fed-batch reactor.
2001 Jul
Fungitoxic activity of 12 essential oils against four postharvest citrus pathogens: chemical analysis of thymus capitatus oil and its effect in subatmospheric pressure conditions.
2001 Jul
Comparison of eucalyptus camaldulensis Dehn. oils from Mozambique as obtained by hydrodistillation and supercritical carbon dioxide extraction.
2001 May
Quantitative analysis of aroma compounds in carrot (Daucus carota L.) cultivars by capillary gas chromatography using large-volume injection technique.
2001 Sep
Correlation between the chemical and genetic relationships among commercial thyme cultivars.
2001 Sep
Interactions between components of the essential oil of Melaleuca alternifolia.
2001 Sep
Composition and antibacterial activity of the essential oils from Satureja wiedemanniana (Lallem.) Velen.
2001 Sep-Oct
Inhibition of the microsomal metabolism of 1,8-cineole in the common brushtail possum (Trichosurus vulpecula) by terpenes and other chemicals.
2002 Dec
Effects of storage conditions on the composition of Citrus tamurana Hort. ex Tanaka (hyuganatsu) essential oil.
2002 Feb
Enhanced fumigant toxicity of p-cymene against Frankliniella occidentalis by simultaneous application of elevated levels of carbon dioxide.
2002 Feb
Correlation between chemical composition and antibacterial activity of essential oils of some aromatic medicinal plants growing in the Democratic Republic of Congo.
2002 Feb
Analysis by gas chromatography-mass spectrometry of the volatile components of Ageratina adenophora Spreng., growing in the Canary Islands.
2002 Feb 22
Modeling the partition of volatile aroma compounds from a cloud emulsion.
2002 Mar 27
In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer.
2002 May 20
Changes in volatile compounds of carrots (Daucus carota L.) during refrigerated and frozen storage.
2003 Aug 27
Analysis of volatile compounds of taperebá (Spondias mombin L.) and cajá (Spondias mombin L.) by simultaneous distillation and extraction (SDE) and solid phase microextraction (SPME).
2003 Feb 26
Highly selective binding of organometallic ruthenium ethylenediamine complexes to nucleic acids: novel recognition mechanisms.
2003 Jan 8
Assessing the separation of neutral plant secondary metabolites by micellar electrokinetic chromatography.
2003 Jul 4
Antibacterial and antifungal activity of juniper berry oil and its selected components.
2003 Mar
Characterisation of odorants emissions from landfills by SPME and GC/MS.
2003 May
Eta6-mesityl,eta1-imidazolinylidene-carbene-ruthenium(II) complexes: catalytic activity of their allenylidene derivatives in alkene metathesis and cycloisomerisation reactions.
2003 May 23
Synthesis and reactions of terminal osmium and ruthenium complexed phosphinidenes [(eta6-Ar)(L)Md=PMes*].
2003 May 23
Bioluminescent bioreporter integrated-circuit sensing of microbial volatile organic compounds.
2003 Nov
Unexpected superoxide dismutase antioxidant activity of ferric chloride in acetonitrile.
2003 Nov 14
Seasonal and phenological variations of the essential oil from the narrow endemic species Artemisia molinieri and its biological activities.
2003 Nov 19
The effects of Eucalyptus terpenes on hepatic cytochrome P450 CYP4A, peroxisomal Acyl CoA oxidase (AOX) and peroxisome proliferator activated receptor alpha (PPARalpha) in the common brush tail possum (Trichosurus vulpecula).
2003 Oct
DNA interactions of monofunctional organometallic ruthenium(II) antitumor complexes in cell-free media.
2003 Oct 7
Emission of volatile organic compounds during composting of municipal solid wastes.
2004 Apr
Phytochemical analysis and in vitro antimicrobial activity of two Satureja species essential oils.
2004 Dec
Effect of some volatile oils on the affinity of intact and oxidized low-density lipoproteins for adrenal cell surface receptors.
2004 Dec
In vitro biological activity and essential oil composition of four indigenous South African Helichrysum species.
2004 Dec
Chemical analysis and antifungal activity of Thymus striatus.
2004 Jan
Antifungal activity of Thymus oils and their major compounds.
2004 Jan
Chemical composition and antifungal activity of the essential oil of Thymbra capitata.
2004 Jun
Combined analysis of the essential oil of Chenopodium ambrosioides by GC, GC-MS and 13C-NMR spectroscopy: quantitative determination of ascaridole, a heat-sensitive compound.
2004 Sep-Oct
The S1 <-- S0 spectrum of jet-cooled p-cymene.
2005 Apr
Application of artificial neural network on mono- and sesquiterpenes compounds determined by headspace solid-phase microextraction-gas chromatography-mass spectrometry for the Piedmont ricotta cheese traceability.
2005 Apr 15
Synthesis, characterization, and photochemical behavior of {Ru(arene)}2+ derivatives of alpha-[PW11O39]7-: an organometallic way to ruthenium-substituted heteropolytungstates.
2005 Apr 18
Insertion reactions of GaCp*, InCp* and In[C(SiMe3)3] into the Ru-Cl bonds of [(p-cymene)RuIICl2]2 and [Cp*RuIICl]4.
2005 Jan 7
Monoterpenes from thyme (Thymus vulgaris) as potential mosquito repellents.
2005 Mar
Effect of solution conductivity on the volatile constituents of Origanum dictamnus L. in nutrient film culture.
2005 Mar 9
Synthetic, spectroscopic, computational and structural studies of some 13-vertex ruthenacarboranes.
2005 May 5
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:11 GMT 2023
Edited
by admin
on Fri Dec 15 15:22:11 GMT 2023
Record UNII
1G1C8T1N7Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CYMENE
FCC   FHFI   HSDB   INCI   MI  
INCI  
Official Name English
CYMENE [MART.]
Common Name English
PARA-CYMENE
Systematic Name English
4-CYMENE
Systematic Name English
NSC-4162
Code English
P-CYMOL
Common Name English
FEMA NO. 2356
Code English
P-METHYLCUMENE
Systematic Name English
P-CYMENE [INCI]
Common Name English
4-ISOPROPYLTOLUENE
Systematic Name English
P-METHYLISOPROPYLBENZENE
Systematic Name English
1-ISOPROPYL-4-METHYLBENZENE
Systematic Name English
1-METHYL-4-(1-METHYLETHYL)BENZENE
Systematic Name English
BENZENE, 1-METHYL-4-(1-METHYLETHYL)-
Systematic Name English
4-ISOPROPYL-1-METHYLBENZENE
Systematic Name English
4-METHYLISOPROPYLBENZENE
Systematic Name English
P-ISOPROPYLTOLUENE
Common Name English
P-CYMENE [FHFI]
Common Name English
P-CYMENE [FCC]
Common Name English
1-METHYL-4-ISOPROPYLBENZENE
Systematic Name English
P-Cymene [WHO-DD]
Common Name English
PARACYMENE
Systematic Name English
P-CYMENE [HSDB]
Common Name English
2-P-TOLYLPROPANE
Systematic Name English
CYMENE, P-
Common Name English
DOLCYMENE
Common Name English
CAMPHOGEN
Common Name English
P-CYMENE [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 122103
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
JECFA EVALUATION P-CYMENE
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
Code System Code Type Description
DAILYMED
1G1C8T1N7Q
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
FDA UNII
1G1C8T1N7Q
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
RXCUI
15002
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID3026645
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
SMS_ID
100000133903
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
MERCK INDEX
m4030
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
202-796-7
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
JECFA MONOGRAPH
1324
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
MESH
C007210
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
PUBCHEM
7463
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
CHEBI
28768
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
EVMPD
SUB56890
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
CAS
99-87-6
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
WIKIPEDIA
P-CYMENE
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
HSDB
5128
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
NSC
4162
Created by admin on Fri Dec 15 15:22:11 GMT 2023 , Edited by admin on Fri Dec 15 15:22:11 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT MAY BE PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT MAY BE PRESENT
PARENT -> CONSTITUENT MAY BE PRESENT
ASSAY (GC)
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
Compound measured as 1.10% of the composition of the steam distillate of Elymus repens rhizome as per R Boesel in Planta Medica iss:4 pg:399-400, 1989.