Showing Compound Card for m-Cymene (CDB000630)

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Record Information
Version1.0
Created at2020-03-19 00:47:36 UTC
Updated at2020-11-18 16:35:21 UTC
CannabisDB IDCDB000630
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common Namem-Cymene
Descriptionm-Cymene also known as 1-Isopropyl-3-methylbenzene, belongs to the class of organic compounds known as cumenes. These are aromatic compounds containing a prop-2-ylbenzene moiety. m-Cymene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring meta-substituted with a methyl group and an isopropyl group. It is a flammable colorless liquid which is nearly insoluble in water but soluble in organic solvents. In addition to m-cymene, there are two other geometric isomers called o-cymene, in which the alkyl groups are ortho-substituted, and p-cymene, in which they are para-substituted. p-Cymene is the most common and only natural isomer. The three isomers form the group of cymenes ( Ref:DOI ; Ref:DOI ). Cymenes can be produced in the laboratory by alkylation of toluene with propylene. m-Cymene has been reported to be present as a volatile component in cannabis samples (PMID: 26657499 ).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Methyl-3-isopropylbenzeneMeSH
1-Methyl-3-(1-methylethyl)-benzeneHMDB
1-Methyl-3-(1-methylethyl)benzeneHMDB
1-Methyl-3-(1-methylethyl)benzene, 9ciHMDB
3-IsopropyltolueneHMDB
3-Methyl-1-isopropylbenzeneHMDB
beta-CymeneHMDB
m-CymeneHMDB
m-CymolHMDB
m-IsopropyltolueneHMDB
m-Mentha-1,3,5-trieneHMDB
m-MethylisopropylbenzeneHMDB
Meta-cymeneHMDB
Chemical FormulaC10H14
Average Molecular Weight134.22
Monoisotopic Molecular Weight134.1096
IUPAC Name1-methyl-3-(propan-2-yl)benzene
Traditional NameM-cymene
CAS Registry Number535-77-3
SMILES
CC(C)C1=CC=CC(C)=C1
InChI Identifier
InChI=1S/C10H14/c1-8(2)10-6-4-5-9(3)7-10/h4-8H,1-3H3
InChI KeyXCYJPXQACVEIOS-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cumenes. These are aromatic compounds containing a prop-2-ylbenzene moiety.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassCumenes
Direct ParentCumenes
Alternative Parents
Substituents
  • Phenylpropane
  • Cumene
  • Toluene
  • Aromatic hydrocarbon
  • Unsaturated hydrocarbon
  • Hydrocarbon
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Route of exposure:

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Biological location:

Role

Biological role:

Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point-63.75 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.042 mg/mL at 25 °CNot Available
logP4.50Not Available
Predicted Properties
PropertyValueSource
logP4.07ALOGPS
logP3.73ChemAxon
logS-3.9ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity45.29 m³·mol⁻¹ChemAxon
Polarizability16.93 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
EI-MSMass Spectrum (Electron Ionization)splash10-014i-3900000000-63e35dd6fd0426ea41152015-03-01View Spectrum
GC-MSm-Cymene, non-derivatized, GC-MS Spectrumsplash10-0016-4900000000-7e22c2f43a675e8f3826Spectrum
GC-MSm-Cymene, non-derivatized, GC-MS Spectrumsplash10-0016-4900000000-7e22c2f43a675e8f3826Spectrum
Predicted GC-MSm-Cymene, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-014l-8900000000-3fd90a831bc2b2eab9b8Spectrum
Predicted GC-MSm-Cymene, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0900000000-666de596259b0d70d4402016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-2900000000-e4c598c7d1a44b8e096c2016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-014i-9600000000-0e9f7bcebf899619c2f32016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0900000000-09b3c3fc331c3d7dbd002016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-0900000000-24da1976a78e69448d432016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00lu-4900000000-f49be135fafd0f5123632016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0900000000-f5fa2e4eafb73a2ce5ef2021-09-22View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-0900000000-0ffbfca8607ff670721d2021-09-22View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-014l-9700000000-34c004e46fe6c9a7f8372021-09-22View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-9100000000-79ea49b7657805a47ec02021-09-22View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-9100000000-aa1b0d085bc864bd9b5a2021-09-22View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00mo-9000000000-ec5ad2fa68c443e310112021-09-22View Spectrum
NMR
TypeDescriptionView
Pathways
Pathways
Protein Targets
EnzymesNot Available
TransportersNot Available
Metal BindingsNot Available
ReceptorsNot Available
Transcriptional FactorsNot Available
Concentrations Data
Not Available
HMDB IDHMDB0037051
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB016033
KNApSAcK IDC00010967
Chemspider ID10355
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound10812
PDB IDNot Available
ChEBI IDNot Available
References
General References
  1. Rice S, Koziel JA: Characterizing the Smell of Marijuana by Odor Impact of Volatile Compounds: An Application of Simultaneous Chemical and Sensory Analysis. PLoS One. 2015 Dec 10;10(12):e0144160. doi: 10.1371/journal.pone.0144160. eCollection 2015. [PubMed:26657499 ]