General Information

Chemical name1,1-Diethoxypropane
CAS number4744-08-5
COE number10018
Flavouring typesubstances
FL No.06.069
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
CID20858
IUPAC Name1,1-diethoxypropane
InChIInChI=1S/C7H16O2/c1-4-7(8-5-2)9-6-3/h7H,4-6H2,1-3H3
InChI KeyMBNMGGKBGCIEGF-UHFFFAOYSA-N
Canonical SMILESCCC(OCC)OCC
Molecular FormulaC7H16O2

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight132.203
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Complexity48.9
CACTVS Substructure Key Fingerprint A A A D c e B g 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 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 Mass132.115
Exact Mass132.115
XLogP3None
XLogP3-AA1.7
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count9
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+0.9578
Human Intestinal AbsorptionHIA+0.9805
Caco-2 PermeabilityCaco2+0.6552
P-glycoprotein SubstrateNon-substrate0.7829
P-glycoprotein InhibitorNon-inhibitor0.8641
Non-inhibitor0.9135
Renal Organic Cation TransporterNon-inhibitor0.8994
Distribution
Subcellular localizationMitochondria0.5972
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8856
CYP450 2D6 SubstrateNon-substrate0.8973
CYP450 3A4 SubstrateNon-substrate0.6866
CYP450 1A2 InhibitorNon-inhibitor0.8105
CYP450 2C9 InhibitorNon-inhibitor0.9350
CYP450 2D6 InhibitorNon-inhibitor0.9331
CYP450 2C19 InhibitorNon-inhibitor0.9326
CYP450 3A4 InhibitorNon-inhibitor0.9452
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7580
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8814
Non-inhibitor0.8699
AMES ToxicityNon AMES toxic0.7852
CarcinogensCarcinogens 0.7933
Fish ToxicityLow FHMT0.5571
Tetrahymena Pyriformis ToxicityLow TPT0.8446
Honey Bee ToxicityHigh HBT0.8191
BiodegradationNot ready biodegradable0.6257
Acute Oral ToxicityIII0.8844
Carcinogenicity (Three-class)Non-required0.6183

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.6340LogS
Caco-2 Permeability1.0333LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.6649LD50, mol/kg
Fish Toxicity2.4637pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.8011pIGC50, 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