Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • p-Menthane-3,8-diol [show]

General Information

MaintermP-MENTHANE-3,8-DIOL
Doc TypeEAF
CAS Reg.No.(or other ID)42822-86-6
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID556998
IUPAC Name2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol
InChIInChI=1S/C10H20O2/c1-7-4-5-8(9(11)6-7)10(2,3)12/h7-9,11-12H,4-6H2,1-3H3
InChI KeyLMXFTMYMHGYJEI-UHFFFAOYSA-N
Canonical SMILESCC1CCC(C(C1)O)C(C)(C)O
Molecular FormulaC10H20O2
Wikipediap-menthane-3,8-diol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight172.268
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Complexity154.0
CACTVS Substructure Key Fingerprint A A A D c e B w M A A A A A A A A A A A A A A A A A A A A A A A A A A w A A A A A A A A A A A A A A A A G g A A C A A A D V S g g A I C A A A A A g A A A A A A A A A A A A A A A A A A A A A A A A A A E A I A A A A A Q A A F A A A A A A G A w P A O g A A A A A A A A A C A A A I A A B A A A A A A A A A A A A = =
Topological Polar Surface Area40.5
Monoisotopic Mass172.146
Exact Mass172.146
XLogP3None
XLogP3-AA2.2
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count12
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count3
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8856
Human Intestinal AbsorptionHIA+0.9865
Caco-2 PermeabilityCaco2+0.7325
P-glycoprotein SubstrateSubstrate0.5679
P-glycoprotein InhibitorNon-inhibitor0.9077
Non-inhibitor0.8545
Renal Organic Cation TransporterNon-inhibitor0.8902
Distribution
Subcellular localizationMitochondria0.6312
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8094
CYP450 2D6 SubstrateNon-substrate0.8257
CYP450 3A4 SubstrateSubstrate0.6435
CYP450 1A2 InhibitorNon-inhibitor0.6966
CYP450 2C9 InhibitorNon-inhibitor0.6604
CYP450 2D6 InhibitorNon-inhibitor0.9401
CYP450 2C19 InhibitorNon-inhibitor0.8445
CYP450 3A4 InhibitorNon-inhibitor0.8967
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9403
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9356
Non-inhibitor0.8383
AMES ToxicityNon AMES toxic0.5927
CarcinogensNon-carcinogens0.8281
Fish ToxicityHigh FHMT0.5794
Tetrahymena Pyriformis ToxicityHigh TPT0.8543
Honey Bee ToxicityHigh HBT0.7454
BiodegradationNot ready biodegradable0.9046
Acute Oral ToxicityIII0.7766
Carcinogenicity (Three-class)Non-required0.6846

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.6070LogS
Caco-2 Permeability1.4482LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.5350LD50, mol/kg
Fish Toxicity2.5203pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.2730pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassPrenol lipids
SubclassMonoterpenoids
Intermediate Tree NodesNot available
Direct ParentMenthane monoterpenoids
Alternative Parents
Molecular FrameworkAliphatic homomonocyclic compounds
SubstituentsP-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexanol - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
DescriptionThis compound 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.

From ClassyFire