Linalyl isovalerate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Linalyl isovalerate |
| CAS number | 1118-27-0 |
| COE number | 449 |
| JECFA number | 363 |
| Flavouring type | substances |
| FL No. | 09.454 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | JECFA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 240119 |
| IUPAC Name | 3,7-dimethylocta-1,6-dien-3-yl 3-methylbutanoate |
| InChI | InChI=1S/C15H26O2/c1-7-15(6,10-8-9-12(2)3)17-14(16)11-13(4)5/h7,9,13H,1,8,10-11H2,2-6H3 |
| InChI Key | WCDGWAIZRYMVOW-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CC(=O)OC(C)(CCC=C(C)C)C=C |
| Molecular Formula | C15H26O2 |
| Wikipedia | linalyl isovalerate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 238.371 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Complexity | 285.0 |
| 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 U S A g A A C C A A A B A C I A i D S C A A A A A A g A A A I C A E A A A g A B B I A I Q A C A A A E g A A I I A I A A A A 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 = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 238.193 |
| Exact Mass | 238.193 |
| XLogP3 | None |
| XLogP3-AA | 4.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 17 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9643 |
| Human Intestinal Absorption | HIA+ | 0.9778 |
| Caco-2 Permeability | Caco2+ | 0.6914 |
| P-glycoprotein Substrate | Non-substrate | 0.6066 |
| P-glycoprotein Inhibitor | Inhibitor | 0.5000 |
| Inhibitor | 0.5953 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8574 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5697 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8838 |
| CYP450 2D6 Substrate | Non-substrate | 0.8960 |
| CYP450 3A4 Substrate | Substrate | 0.6184 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6859 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8363 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9384 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7095 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8653 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8114 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9193 |
| Non-inhibitor | 0.9194 | |
| AMES Toxicity | Non AMES toxic | 0.9401 |
| Carcinogens | Carcinogens | 0.5670 |
| Fish Toxicity | High FHMT | 0.9409 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9798 |
| Honey Bee Toxicity | High HBT | 0.8839 |
| Biodegradation | Ready biodegradable | 0.8253 |
| Acute Oral Toxicity | III | 0.7808 |
| Carcinogenicity (Three-class) | Non-required | 0.5112 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.8137 | LogS |
| Caco-2 Permeability | 1.2306 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5432 | LD50, mol/kg |
| Fish Toxicity | 0.6562 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5572 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic monoterpenoids |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic monoterpenoid - Fatty acid ester - Fatty acyl - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. |
From ClassyFire