Citronellyl oxyacetaldehyde
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Citronellyl oxyacetaldehyde |
| CAS number | 7492-67-3 |
| COE number | 2012 |
| JECFA number | 592 |
| Flavouring type | substances |
| FL No. | 05.079 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | At least 75%; secondary components 20-21% geranyloxyacetaldehyde; 1-2% citronellol |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61401 |
| IUPAC Name | 2-(3,7-dimethyloct-6-enoxy)acetaldehyde |
| InChI | InChI=1S/C12H22O2/c1-11(2)5-4-6-12(3)7-9-14-10-8-13/h5,8,12H,4,6-7,9-10H2,1-3H3 |
| InChI Key | LMETVDMCIJNNKH-UHFFFAOYSA-N |
| Canonical SMILES | CC(CCC=C(C)C)CCOCC=O |
| Molecular Formula | C12H22O2 |
| Wikipedia | citronelloxyacetaldehyde |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 198.306 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Complexity | 169.0 |
| 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 g g A I C A A A A B A C I A i h S g A I A A A A g A A A A C A B A A A g A A A I A A Q Q C A A A E g A A I A A O A Q A A O 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 | 198.162 |
| Exact Mass | 198.162 |
| XLogP3 | None |
| XLogP3-AA | 3.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 14 |
| 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+ | 0.9430 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.6493 |
| P-glycoprotein Substrate | Substrate | 0.5646 |
| P-glycoprotein Inhibitor | Inhibitor | 0.5319 |
| Inhibitor | 0.5188 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8058 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5629 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8774 |
| CYP450 2D6 Substrate | Non-substrate | 0.8342 |
| CYP450 3A4 Substrate | Substrate | 0.5392 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8232 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9300 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9409 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8770 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9649 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9269 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8094 |
| Non-inhibitor | 0.7784 | |
| AMES Toxicity | Non AMES toxic | 0.7503 |
| Carcinogens | Carcinogens | 0.5707 |
| Fish Toxicity | High FHMT | 0.9146 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9913 |
| Honey Bee Toxicity | High HBT | 0.7919 |
| Biodegradation | Ready biodegradable | 0.8439 |
| Acute Oral Toxicity | III | 0.8610 |
| Carcinogenicity (Three-class) | Non-required | 0.5487 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.7849 | LogS |
| Caco-2 Permeability | 1.3013 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5670 | LD50, mol/kg |
| Fish Toxicity | 0.8741 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4645 | 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 - Ether - Dialkyl ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - 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