4,6,9-Trimethyl-3,5,8,10-tetraoxadodecane

Odors

Receptor Interaction

No receptors available

General Information

Common Name: 4,6,9-Trimethyl-3,5,8,10-tetraoxadodecane
IUPAC Name: 1,2-bis(1-ethoxyethoxy)propane
Molecular Formula: C7H8N2O
SMILES: CCOC(C)OCC(C)OC(C)OCC
Inchi: 1S/C11H24O4/c1-6-12-10(4)14-8-9(3)15-11(5)13-7-2/h9-11H,6-8H2,1-5H3
Inchi Key: TZVJNJVDGXFMCF-UHFFFAOYSA-N
Cas No: 67715-79-1

Functional Group

Ethers

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 3
Veber Violations 0
Egan Violations 0
Muegge Violations 1

Cross References

PubChem: 5362566
Zinc: ZINC2598052
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 136.15
Mass (g/mol) 220.167
Molar Refractivity 37.19
Net Charge
HBD
HBA 3
Rt Bonds 1
Rings
TPSA 42.85
Hetero Atoms 4
Heavy Atoms 10
Aromatic Heavy Atoms 6
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 236.00 to 237.00
Vapor Pressure (mmHg@25.00 °C) 0.066
Vapor Density (Air =1)
Fraction Csp3 0.29
LogP 2.173
iLOGP 1.72
XLOGP3 0.62
WLOGP 0.99
MLOGP -0.35
ESOL Log S -1.45
ESOL Solubility (mg/ml) 4.8
ESOL Solubility (mol/l) 0.035
ESOL Class: esol_class Very soluble
Ali Log S -1.09
Ali Solubility (mg/ml) 11
Ali Solubility (mol/l) 0.08
Ali Class Very soluble
Silicos-IT LogSw -2.34
Silicos-IT Solubility (mg/ml) 0.62
Silicos-IT Solubility (mol/l) 0
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -6.69
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.257
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.426
Carcinogenicity (Binary) 1
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 0
Androgen Receptor Binding 0
Aromatase Binding 0
Estrogen Receptor Binding 0
Glucocorticoid Receptor Binding 0
Thyroid Receptor Binding 0
BRCP inhibitor 0
BSEP inhibitor 0
OATP1B1 inhibitor 1
OATP1B3 inhibitor 1
OATP2B1 inhibitor 0
OCT1 inhibitor 0
OCT2 inhibitor 0