Record Information
Version1.0
Creation date2010-04-08 22:12:10 UTC
Update date2019-11-26 03:12:34 UTC
Primary IDFDB015991
Secondary Accession NumbersNot Available
Chemical Information
FooDB Namep-Mentha-1,3,8-triene
Descriptionp-Mentha-1,3,8-triene, also known as 1,3,8-menthatriene, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. Based on a literature review a significant number of articles have been published on p-Mentha-1,3,8-triene.
CAS Number18368-95-1
Structure
Thumb
Synonyms
SynonymSource
1,3,8-MenthatrieneChEBI
1,3,8-p-MenthatrieneChEBI
1,3,8-Para-menthatrieneChEBI
1-Isopropenyl-4-methyl-1,3-cyclohexadieneChEBI
1-Methyl-4-(1-methylethenyl)-1,3-cyclohexadieneChEBI
1-Methyl-4-prop-1-en-2-ylcyclohexa-1,3-dieneChEBI
2-Methyl-5-(1-methylethenyl)-1,3-cyclohexadieneChEBI
p-1,3,8-MenthatrieneChEBI
p-MenthatrieneChEBI
1-Methyl-4-(1-methylethenyl)-1,3-cyclohexadiene, 9ciHMDB
P-Menta-1,3,8-trieneHMDB
1-Methyl-4-(1-methylethenyl)-1,3-cyclohexadiene, 9CIdb_source
1,3-Cyclohexadiene, 2-methyl-5-(1-methylethenyl)-biospider
1,3,8-menthatrienebiospider
1,3,8-p-menthatrienebiospider
1,3,8-para-Menthatrienebiospider
p-Menta-1,3,8-trienebiospider
Predicted Properties
PropertyValueSource
Water Solubility0.79 g/LALOGPS
logP4.15ALOGPS
logP2.81ChemAxon
logS-2.2ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity47.33 m³·mol⁻¹ChemAxon
Polarizability16.98 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Chemical FormulaC10H14
IUPAC name1-methyl-4-(prop-1-en-2-yl)cyclohexa-1,3-diene
InChI IdentifierInChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4,6H,1,5,7H2,2-3H3
InChI KeyXNMPFDIYAMOYRM-UHFFFAOYSA-N
Isomeric SMILESCC(=C)C1=CC=C(C)CC1
Average Molecular Weight134.2182
Monoisotopic Molecular Weight134.109550448
Classification
Description Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassMonoterpenoids
Direct ParentMenthane monoterpenoids
Alternative Parents
Substituents
  • P-menthane monoterpenoid
  • Monocyclic monoterpenoid
  • Branched unsaturated hydrocarbon
  • Cyclic olefin
  • Unsaturated aliphatic hydrocarbon
  • Unsaturated hydrocarbon
  • Olefin
  • Hydrocarbon
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Route of exposure:

Source:

Biological location:

Process

Naturally occurring process:

Role

Industrial application:

Biological role:

Physico-Chemical Properties - Experimental
Physico-Chemical Properties - Experimental
PropertyValueReference
Physical stateNot Available
Physical DescriptionNot Available
Mass CompositionC 89.49%; H 10.51%DFC
Melting PointNot Available
Boiling PointBp5 65°DFC
Experimental Water SolubilityNot Available
Experimental logPNot Available
Experimental pKaNot Available
Isoelectric pointNot Available
ChargeNot Available
Optical RotationNot Available
Spectroscopic UV DataNot Available
DensityNot Available
Refractive Indexn20D 1.5395DFC
Spectra
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MSp-Mentha-1,3,8-triene, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-00kf-9600000000-d140fb4269c347dba18dSpectrum
Predicted GC-MSp-Mentha-1,3,8-triene, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-1900000000-6ea5f925c63347b30ffeSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-8900000000-388bb713ade30bdddfc4Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0uxr-9100000000-3a38e9d0361d1eaadc21Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0900000000-7c744902d6088923ed28Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-0900000000-ec06062b3ca66d737e74Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0159-4900000000-45776dc5b5f67b50e4d8Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-052r-2900000000-388a572ccdaae3d6acb3Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-054o-9200000000-835a215b0892cd66365dSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00ou-9000000000-3fb623fa7f2a7efd5cebSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0900000000-f5fa2e4eafb73a2ce5efSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-0900000000-614538eb198b53b54f50Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-014i-4900000000-fe406cd95ad2315d928bSpectrum
NMRNot Available
ChemSpider ID154138
ChEMBL IDNot Available
KEGG Compound IDNot Available
Pubchem Compound ID176983
Pubchem Substance IDNot Available
ChEBI IDNot Available
Phenol-Explorer IDNot Available
DrugBank IDNot Available
HMDB IDHMDB37013
CRC / DFC (Dictionary of Food Compounds) IDKLW24-S:KLW24-S
EAFUS IDNot Available
Dr. Duke IDP-MENTHA-1,3,8-TRIENE|P-MENTHATRIENE|1,3,8-P-MENTHATRIENE
BIGG IDNot Available
KNApSAcK IDC00010907
HET IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
Flavornet ID18368-95-1
GoodScent IDrw1551761
SuperScent IDNot Available
Wikipedia IDNot Available
Phenol-Explorer Metabolite IDNot Available
Duplicate IDSNot Available
Old DFC IDSNot Available
Associated Foods
FoodContent Range AverageReference
FoodReference
Biological Effects and Interactions
Health Effects / BioactivitiesNot Available
EnzymesNot Available
PathwaysNot Available
MetabolismNot Available
BiosynthesisNot Available
Organoleptic Properties
Flavours
FlavorCitations
turpentine
  1. Arn, H, Acree TE. “Flavornet: A database of aroma compounds based on odor potency in natural products”. Developments in Food Science 40 (1998): 27. doi:10.1016/S0167-4501(98)80029-0
  2. The Good Scents Company (2009). Flavor and fragrance information catalog. <http://www.thegoodscentscompany.com/allprod.html> Accessed 15.10.23.
camphor
  1. The Good Scents Company (2009). Flavor and fragrance information catalog. <http://www.thegoodscentscompany.com/allprod.html> Accessed 15.10.23.
herbal
  1. The Good Scents Company (2009). Flavor and fragrance information catalog. <http://www.thegoodscentscompany.com/allprod.html> Accessed 15.10.23.
woody
  1. The Good Scents Company (2009). Flavor and fragrance information catalog. <http://www.thegoodscentscompany.com/allprod.html> Accessed 15.10.23.
Files
MSDSNot Available
References
Synthesis ReferenceNot Available
General ReferenceNot Available
Content Reference— Duke, James. 'Dr. Duke's Phytochemical and Ethnobotanical Databases. United States Department of Agriculture.' Agricultural Research Service, Accessed April 27 (2004).
— Shinbo, Y., et al. 'KNApSAcK: a comprehensive species-metabolite relationship database.' Plant Metabolomics. Springer Berlin Heidelberg, 2006. 165-181.