General Information

Chemical name1,1-Diethoxy-2-methylpropane
CAS number1741-41-9
COE number10015
Flavouring typesubstances
FL No.06.058
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
CID519415
IUPAC Name1,1-diethoxy-2-methylpropane
InChIInChI=1S/C8H18O2/c1-5-9-8(7(3)4)10-6-2/h7-8H,5-6H2,1-4H3
InChI KeyKZDFOVZPOBSHDH-UHFFFAOYSA-N
Canonical SMILESCCOC(C(C)C)OCC
Molecular FormulaC8H18O2

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight146.23
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Complexity65.7
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 D Q 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 A A A A A i A A A A A A A E 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 = =
Topological Polar Surface Area18.5
Monoisotopic Mass146.131
Exact Mass146.131
XLogP3None
XLogP3-AA2.2
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+0.9446
Human Intestinal AbsorptionHIA+0.9877
Caco-2 PermeabilityCaco2+0.6486
P-glycoprotein SubstrateNon-substrate0.8003
P-glycoprotein InhibitorNon-inhibitor0.8724
Non-inhibitor0.8401
Renal Organic Cation TransporterNon-inhibitor0.8984
Distribution
Subcellular localizationMitochondria0.5591
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8760
CYP450 2D6 SubstrateNon-substrate0.8884
CYP450 3A4 SubstrateNon-substrate0.6617
CYP450 1A2 InhibitorNon-inhibitor0.8574
CYP450 2C9 InhibitorNon-inhibitor0.9331
CYP450 2D6 InhibitorNon-inhibitor0.9454
CYP450 2C19 InhibitorNon-inhibitor0.9440
CYP450 3A4 InhibitorNon-inhibitor0.9856
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8244
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9426
Non-inhibitor0.9277
AMES ToxicityNon AMES toxic0.9219
CarcinogensCarcinogens 0.8103
Fish ToxicityHigh FHMT0.6022
Tetrahymena Pyriformis ToxicityLow TPT0.8735
Honey Bee ToxicityHigh HBT0.8491
BiodegradationReady biodegradable0.5409
Acute Oral ToxicityIII0.7221
Carcinogenicity (Three-class)Non-required0.6039

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.5355LogS
Caco-2 Permeability1.1268LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.3274LD50, mol/kg
Fish Toxicity2.5262pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.2388pIGC50, 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