General Information

Chemical name1,1-Dimethoxyhexane
CAS number1599-47-9
Flavouring typesubstances
FL No.06.073
MixtureNo
Purity of the named substance at least 95% unless otherwise specified
Reference bodyEFSA

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID74137
IUPAC Name1,1-dimethoxyhexane
InChIInChI=1S/C8H18O2/c1-4-5-6-7-8(9-2)10-3/h8H,4-7H2,1-3H3
InChI KeyZQUJUCJLDXTKKW-UHFFFAOYSA-N
Canonical SMILESCCCCCC(OC)OC
Molecular FormulaC8H18O2

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight146.23
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count6
Complexity60.3
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 A A A A A A A A A A A A A A A A A G g A A A A A A C A C w g A M C C A A A B 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 Q A A I A A A A g A A A E A A A A A A G A Q 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 A A A A A A A = =
Topological Polar Surface Area18.5
Monoisotopic Mass146.131
Exact Mass146.131
XLogP3None
XLogP3-AA2.4
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count10
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
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+0.9849
Human Intestinal AbsorptionHIA+0.9755
Caco-2 PermeabilityCaco2+0.7725
P-glycoprotein SubstrateNon-substrate0.7177
P-glycoprotein InhibitorNon-inhibitor0.8640
Non-inhibitor0.8784
Renal Organic Cation TransporterNon-inhibitor0.9146
Distribution
Subcellular localizationMitochondria0.4048
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8518
CYP450 2D6 SubstrateNon-substrate0.8676
CYP450 3A4 SubstrateNon-substrate0.6072
CYP450 1A2 InhibitorNon-inhibitor0.7097
CYP450 2C9 InhibitorNon-inhibitor0.9198
CYP450 2D6 InhibitorNon-inhibitor0.9418
CYP450 2C19 InhibitorNon-inhibitor0.9183
CYP450 3A4 InhibitorNon-inhibitor0.9754
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8750
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8863
Non-inhibitor0.8648
AMES ToxicityNon AMES toxic0.9205
CarcinogensCarcinogens 0.6264
Fish ToxicityHigh FHMT0.5084
Tetrahymena Pyriformis ToxicityLow TPT0.7072
Honey Bee ToxicityHigh HBT0.8114
BiodegradationReady biodegradable0.6900
Acute Oral ToxicityIII0.9475
Carcinogenicity (Three-class)Non-required0.6500

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.6786LogS
Caco-2 Permeability1.2779LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.5327LD50, mol/kg
Fish Toxicity1.6614pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.1630pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassEthers
Intermediate Tree NodesNot available
Direct ParentAcetals
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsAcetal - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as acetals. These are compounds having the structure R2C(OR')2 ( R' not Hydrogen) and thus diethers of geminal diols. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R' groups.

From ClassyFire