General Information

Chemical name1,1-Di-isobutoxy-3-methylbutane
CAS number13439-98-0
COE number10024
Flavouring typesubstances
FL No.06.124
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
CID83453
IUPAC Name3-methyl-1,1-bis(2-methylpropoxy)butane
InChIInChI=1S/C13H28O2/c1-10(2)7-13(14-8-11(3)4)15-9-12(5)6/h10-13H,7-9H2,1-6H3
InChI KeyXQJQKXSIFKNEPF-UHFFFAOYSA-N
Canonical SMILESCC(C)CC(OCC(C)C)OCC(C)C
Molecular FormulaC13H28O2
Wikipedia1,1-di-isobutoxy-3-methylbutane

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight216.365
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count8
Complexity130.0
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 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 E A A A E A A A A A A A I 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 Mass216.209
Exact Mass216.209
XLogP3None
XLogP3-AA4.4
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count15
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+0.9522
Human Intestinal AbsorptionHIA+0.9839
Caco-2 PermeabilityCaco2+0.6335
P-glycoprotein SubstrateNon-substrate0.7754
P-glycoprotein InhibitorNon-inhibitor0.8881
Non-inhibitor0.9043
Renal Organic Cation TransporterNon-inhibitor0.8980
Distribution
Subcellular localizationMitochondria0.6989
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8643
CYP450 2D6 SubstrateNon-substrate0.8824
CYP450 3A4 SubstrateNon-substrate0.6575
CYP450 1A2 InhibitorNon-inhibitor0.8794
CYP450 2C9 InhibitorNon-inhibitor0.9351
CYP450 2D6 InhibitorNon-inhibitor0.9468
CYP450 2C19 InhibitorNon-inhibitor0.9208
CYP450 3A4 InhibitorNon-inhibitor0.9721
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8898
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9061
Non-inhibitor0.9251
AMES ToxicityNon AMES toxic0.8603
CarcinogensCarcinogens 0.7702
Fish ToxicityHigh FHMT0.8303
Tetrahymena Pyriformis ToxicityHigh TPT0.5415
Honey Bee ToxicityHigh HBT0.8241
BiodegradationNot ready biodegradable0.6878
Acute Oral ToxicityIII0.8088
Carcinogenicity (Three-class)Non-required0.5293

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.5218LogS
Caco-2 Permeability1.1640LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.6549LD50, mol/kg
Fish Toxicity1.8659pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.5340pIGC50, 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