p-Mentha-1,3,5,8-tetraene

Common Name

p-Mentha-1,3,5,8-tetraene Description

p-Mentha-1,3,5,8-tetraene is found in citrus. p-Mentha-1,3,5,8-tetraene occurs in Chamaecyparis, Citrus, Eucalyptus, Juniperus and Ribes species oils and juices. p-Mentha-1,3,5,8-tetraene is a flavouring ingredientP-mentha-1,3,5,8-tetraene belongs to the family of Monocyclic Monoterpenes. These are monoterpenes containing 1 ring in the isoprene chain. Structure

MOLSDFPDBSMILESInChI

Structure for HMDB29641 (p-Mentha-1,3,5,8-tetraene)

Synonyms

Value Source 1-Isopropenyl-4-methylbenzeneHMDB 1-Methyl-4-(1-methylethenyl)-benzeneHMDB 1-Methyl-4-(1-methylethenyl)benzeneHMDB 1-Methyl-4-(1-methylethenyl)benzene, 9ciHMDB 1-Methyl-4-isopropenylbenzeneHMDB 1-Methyl-4alpha-methylstyreneHMDB 2-(4-Methylphenyl)propeneHMDB 2-(P-Methylphenyl)propeneHMDB 2-P-TolylpropeneHMDB 4-IsopropenyltolueneHMDB 4-Methyl-alpha-methylstyreneHMDB 4-MethylisopropenylbenzeneHMDB alpha,4-DimethylstyreneHMDB alpha,P-DimethylstyreneHMDB alpha-Dimethyl-P-styreneHMDB alpha-Methyl-P-methylstyreneHMDB alpha-P DimethylstyreneHMDB CymeneneHMDB dehydro-P-CymeneHMDB FEMA 3144HMDB Ghl.PD_Mitscher_leg0.317HMDB Isopropenyl toluene cHMDB Methyl-4-(1-methylethenyl)-benzeneHMDB Methyl-P-isopropenylbenzeneHMDB P,a-Dimethylstyrene, 8ciHMDB P,alpha-Dimethyl-styreneHMDB P,alpha-DimethylstyreneHMDB P,alpha-DimethylstyrolHMDB P-alpha-Dimethyl-styreneHMDB P-alpha-DimethylstyreneHMDB P-CymeneneHMDB P-Isopropenyl tolueneHMDB P-IsopropenyltolueneHMDB P-Methyl-alpha-methylstyreneHMDB Para- alpha-dimethylstyreneHMDB

Chemical Formlia

C10H12 Average Molecliar Weight

132.2023 Monoisotopic Molecliar Weight

132.093900384 IUPAC Name

1-methyl-4-(prop-1-en-2-yl)benzene Traditional Name

1-methyl-4-(prop-1-en-2-yl)benzene CAS Registry Number

1195-32-0 SMILES

CC(=C)C1=CC=C(C)C=C1

InChI Identifier

InChI=1S/C10H12/c1-8(2)10-6-4-9(3)5-7-10/h4-7H,1H2,2-3H3

InChI Key

MMSLOZQEMPDGPI-UHFFFAOYSA-N Chemical Taxonomy Description

This compound belongs to the class of organic compounds known as phenylpropenes. These are compounds containing a phenylpropene moiety, which consists of a propene substituent bound to a phenyl group. Kingdom

Organic compounds Super Class

Benzenoids Class

Benzene and substituted derivatives Sub Class

Phenylpropenes Direct Parent

Phenylpropenes Alternative Parents

  • Styrenes
  • Toluenes
  • Cyclic olefins
  • Substituents

  • Phenylpropene
  • Styrene
  • Toluene
  • Cyclic olefin
  • Olefin
  • Hydrocarbon
  • Aromatic homomonocyclic compound
  • Molecliar Framework

    Aromatic homomonocyclic compounds External Descriptors

    Not Available Ontology Status

    Detected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

  • Cell signaling
  • Fuel and energy storage
  • Fuel or energy source
  • Membrane integrity/stability
  • Application

  • Flavoring Agent
  • Nutrient
  • Stabilizers
  • Surfactants and Emlisifiers
  • Cellliar locations

  • Extracellliar
  • Membrane
  • Physical Properties State

    Liquid Experimental Properties

    Property Value Reference Melting Point-20 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.16 mg/mLALOGPS logP3.79ALOGPS logP3.52ChemAxon logS-2.9ALOGPS Physiological Charge0ChemAxon Hydrogen Acceptor Count0ChemAxon Hydrogen Donor Count0ChemAxon Polar Surface Area0 Å2ChemAxon Rotatable Bond Count1ChemAxon Refractivity45.07 m3·mol-1ChemAxon Polarizability16.35 Å3ChemAxon Number of Rings1ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Spectrum Type Description Splash Key Predicted GC-MS

    Predicted GC-MS Spectrum – GC-MSNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, NegativeNot Available MS

    Mass Spectrum (Electron Ionization)splash10-014i-7900000000-8a35d379c53b742012dbView in MoNA

    Biological Properties Cellliar Locations

  • Extracellliar
  • Membrane
  • Biofluid Locations

  • Feces
  • Saliva
  • Urine
  • Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations

    Biofluid Status Value Age Sex Condition Reference Details FecesDetected but not Quantified Adlit (>18 years old)Both

    Normal

  • 17314143
  • details FecesDetected but not Quantified Adlit (>18 years old)Both

    Normal

  • 19167006
  • details SalivaDetected but not Quantified Adlit (>18 years old)Not SpecifiedNormal

  • 24421258
  • details UrineDetected but not Quantified Adlit (>18 years old)Both

    Normal

  • 24023812
  • details

    Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB000812 KNApSAcK ID

    C00010905 Chemspider ID

    56173 KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB29641 Metagene Link

    HMDB29641 METLIN ID

    Not Available PubChem Compound

    62385 PDB ID

    Not Available ChEBI ID

    Not Available

    Product: Evatanepag

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 15685200