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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
Self-assembled organometallic [12]metallacrown-3 complexes.
2001 Aug 3
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
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
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
Analysis by gas chromatography-mass spectrometry of the volatile components of Ageratina adenophora Spreng., growing in the Canary Islands.
2002 Feb 22
Determination of monoterpene hydrocarbons and alcohols in Majorana hortensis Moench by micellar electrokinetic capillary chromatographic.
2002 Jul 17
GC/MS evaluation of thyme (Thymus vulgaris L.) oil composition and variations during the vegetative cycle.
2002 Jul 20
Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.
2002 Jun
Microsomal metabolism and enzyme kinetics of the terpene p-cymene in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus) and rat.
2002 May
In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer.
2002 May 20
Bacterial susceptibility to and chemical composition of essential oils from Thymus kotschyanus and Thymus persicus.
2003 Apr 9
Expansion of growth substrate range in Pseudomonas putida F1 by mutations in both cymR and todS, which recruit a ring-fission hydrolase CmtE and induce the tod catabolic operon, respectively.
2003 Mar
Eta6-mesityl,eta1-imidazolinylidene-carbene-ruthenium(II) complexes: catalytic activity of their allenylidene derivatives in alkene metathesis and cycloisomerisation reactions.
2003 May 23
Phytochemical analysis and in vitro antimicrobial activity of two Satureja species essential oils.
2004 Dec
Metabolic engineering of monoterpene biosynthesis: two-step production of (+)-trans-isopiperitenol by tobacco.
2004 Jul
Chemical composition and antifungal activity of the essential oil of Thymbra capitata.
2004 Jun
Water-soluble ruthenium(II) catalysts [RuCl2(eta6-arene)[P(CH2OH)3]] for isomerization of allylic alcohols and alkyne hydration.
2004 Nov 7
Antimicrobial activity, essential oil composition and micromorphology of trichomes of Satureja laxiflora C. Koch from Iran.
2004 Nov-Dec
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
Conformation of DNA modified by monofunctional Ru(II) arene complexes: recognition by DNA binding proteins and repair. Relationship to cytotoxicity.
2005 Jan
New insight into solvent effects on the formal HOO. + HOO. reaction.
2005 Mar 4
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 16 16:54:43 UTC 2022
Edited
by admin
on Fri Dec 16 16:54:43 UTC 2022
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 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
JECFA EVALUATION P-CYMENE
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
CFR 21 CFR 172.515
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
Code System Code Type Description
DAILYMED
1G1C8T1N7Q
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
FDA UNII
1G1C8T1N7Q
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
RXCUI
15002
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY RxNorm
EPA CompTox
DTXSID3026645
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
MERCK INDEX
M4030
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY Merck Index
ECHA (EC/EINECS)
202-796-7
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
MESH
C007210
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
PUBCHEM
7463
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
CHEBI
28768
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
EVMPD
SUB56890
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
CAS
99-87-6
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
WIKIPEDIA
P-CYMENE
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
HSDB
5128
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
NSC
4162
Created by admin on Fri Dec 16 16:54:43 UTC 2022 , Edited by admin on Fri Dec 16 16:54:43 UTC 2022
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT MAY BE PRESENT
ASSAY (GC)
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 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.