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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
Effects of volatile oil constituents of Nigella sativa on carbon tetrachloride-induced hepatotoxicity in mice: evidence for antioxidant effects of thymoquinone.
2001
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
Essential oil composition of sea fennel (Crithmum maritimum) form Turkey.
2001 Oct
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
[Analysis of flavonoids in the flowers and leaves of Monarda didyma L].
2002
SPME applied to the study of volatile organic compounds emitted by three species of Eucalyptus in situ. Solid-phase micro extraction.
2002 Dec 4
Influence of nitrogen fertilizers on the yield and composition of thyme (Thymus vulgaris).
2003 Dec 17
Composition and antibacterial activity of the essential oil of Satureja parnassica subsp parnassica.
2003 Mar
Bioluminescent bioreporter integrated-circuit sensing of microbial volatile organic compounds.
2003 Nov
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
Chemical composition of the fixed and volatile oils of Nigella sativa L. from Iran.
2003 Sep-Oct
In vitro biological activity and essential oil composition of four indigenous South African Helichrysum species.
2004 Dec
Metabolic engineering of monoterpene biosynthesis: two-step production of (+)-trans-isopiperitenol by tobacco.
2004 Jul
Thymus fontanesii Boiss. & Reut.--A potential source of thymol-rich essential oil in North Africa.
2004 Mar-Apr
Essential oil composition of the leaves and stems of Meum athamanticum Jacq., from Spain.
2004 May 21
Water-soluble ruthenium(II) catalysts [RuCl2(eta6-arene)[P(CH2OH)3]] for isomerization of allylic alcohols and alkyne hydration.
2004 Nov 7
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 Sep-Oct
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
New insight into solvent effects on the formal HOO. + HOO. reaction.
2005 Mar 4
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:11 UTC 2023
Edited
by admin
on Fri Dec 15 15:22:11 UTC 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 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
JECFA EVALUATION P-CYMENE
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
Code System Code Type Description
DAILYMED
1G1C8T1N7Q
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
FDA UNII
1G1C8T1N7Q
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
RXCUI
15002
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID3026645
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
SMS_ID
100000133903
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
MERCK INDEX
m4030
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
202-796-7
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
JECFA MONOGRAPH
1324
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
MESH
C007210
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
PUBCHEM
7463
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
CHEBI
28768
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
EVMPD
SUB56890
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
CAS
99-87-6
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
WIKIPEDIA
P-CYMENE
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
HSDB
5128
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 2023
PRIMARY
NSC
4162
Created by admin on Fri Dec 15 15:22:11 UTC 2023 , Edited by admin on Fri Dec 15 15:22:11 UTC 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.