Ethyl 3,5,5-trimethylhexanoate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: Ethyl 3,5,5-trimethylhexanoate
IUPAC Name: ethyl 3,5,5-trimethylhexanoate
Molecular Formula: C7H13NS
SMILES: CCOC(=O)CC(C)CC(C)(C)C
Inchi: 1S/C11H22O2/c1-6-13-10(12)7-9(2)8-11(3,4)5/h9H,6-8H2,1-5H3
Inchi Key: NMZMQQBBZRGLPJ-UHFFFAOYSA-N
Cas No: 67707-75-9

Functional Group

Esters

Drug Likeness

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

Cross References

PubChem: 3017783
Zinc: ZINC2565713
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 143.25
Mass (g/mol) 186.162
Molar Refractivity 48.25
Net Charge
HBD
HBA 1
Rt Bonds 1
Rings
TPSA 37.66
Hetero Atoms 2
Heavy Atoms 9
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 83.00 to 85.00
Vapor Pressure (mmHg@25.00 °C) 0.47
Vapor Density (Air =1)
Fraction Csp3 0.86
LogP 3.012
iLOGP 2.23
XLOGP3 1.86
WLOGP 1.80
MLOGP 1.35
ESOL Log S -1.83
ESOL Solubility (mg/ml) 2.1
ESOL Solubility (mol/l) 0.015
ESOL Class: esol_class Very soluble
Ali Log S -2.27
Ali Solubility (mg/ml) 0.77
Ali Solubility (mol/l) 0.01
Ali Class Soluble
Silicos-IT LogSw -1.81
Silicos-IT Solubility (mg/ml) 2.22
Silicos-IT Solubility (mol/l) 0.02
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.85
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.563
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.738
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Warning
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