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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

2020
742
PubMed

PubMed

TitleDatePubMed
[Chemical constituents in volatile oil from fruits of Alpinia oxyphylla Miq].
2001 Apr
In vivo measurement of flavour release from mixed phase gels.
2001 May
Identification of odoriferous compounds from adults of a swallowtail butterfly, Papilio machaon (Lepidoptera: Papilionidae).
2001 Nov-Dec
Effects of storage conditions on the composition of Citrus tamurana Hort. ex Tanaka (hyuganatsu) essential oil.
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
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
Eta6-mesityl,eta1-imidazolinylidene-carbene-ruthenium(II) complexes: catalytic activity of their allenylidene derivatives in alkene metathesis and cycloisomerisation reactions.
2003 May 23
Chemical composition of the fixed and volatile oils of Nigella sativa L. from Iran.
2003 Sep-Oct
Essential oils: their antibacterial properties and potential applications in foods--a review.
2004 Aug 1
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
Luminescent piano-stool complexes incorporating 1-(4-cyanophenyl)imidazole: synthesis, spectral, and structural studies.
2004 Dec 27
Amphiphilic ruthenium sensitizers and their applications in dye-sensitized solar cells.
2004 Jul 12
Chemical constituents, antifungal and antioxidative effects of ajwain essential oil and its acetone extract.
2004 Jun 2
Arene-ruthenium complexes with salicyloxazolines: diastereoselective synthesis, configurational stability and applications as asymmetric catalysts for Diels-Alder reactions.
2004 May 7
Antimicrobial activity, essential oil composition and micromorphology of trichomes of Satureja laxiflora C. Koch from Iran.
2004 Nov-Dec
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
Monoterpenes from thyme (Thymus vulgaris) as potential mosquito repellents.
2005 Mar
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

Patents

04163747
2
04338318
1
04431841
1
05079386
2
05292719
2
06121182
3
06156692
1
06159890
1
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
DWARF PINE OIL
PARENT -> CONSTITUENT MAY BE PRESENT
CORIANDER OIL
PARENT -> CONSTITUENT ALWAYS PRESENT
PEUMUS BOLDUS LEAF
PARENT -> CONSTITUENT ALWAYS PRESENT
CINNAMON
PARENT -> CONSTITUENT ALWAYS PRESENT
TEA TREE OIL
PARENT -> CONSTITUENT ALWAYS PRESENT
PINE NEEDLE OIL (PINUS MUGO)
PARENT -> CONSTITUENT MAY BE PRESENT
MANDARIN OIL
PARENT -> CONSTITUENT MAY BE PRESENT
ASSAY (GC)
MELALEUCA DISSITIFLORA LEAF OIL
PARENT -> CONSTITUENT ALWAYS PRESENT
ELYMUS REPENS ROOT
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.
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