Z-8-Tetradecenal
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Z-8-Tetradecenal |
| CAS number | 169054-69-7 |
| JECFA number | 1640 |
| Flavouring type | substances |
| FL No. | 05.208 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 6430188 |
| IUPAC Name | (Z)-tetradec-8-enal |
| InChI | InChI=1S/C14H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h6-7,14H,2-5,8-13H2,1H3/b7-6- |
| InChI Key | XAFLGQFKKHZYMU-SREVYHEPSA-N |
| Canonical SMILES | CCCCCC=CCCCCCCC=O |
| Molecular Formula | C14H26O |
| Wikipedia | (8Z)-8-tetradecenal |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 210.361 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 11 |
| Complexity | 149.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w 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 A A A A A A A A A A A A A G g A A A A A A C A C g g A I C A A A A A A C I A C h S g A A A A A A g A A A I C A E A A A g A A B I A A Q A A A A A A g A A I A A M I i I C 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 = = |
| Topological Polar Surface Area | 17.1 |
| Monoisotopic Mass | 210.198 |
| Exact Mass | 210.198 |
| XLogP3 | None |
| XLogP3-AA | 5.0 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| 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+ | 0.9853 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8653 |
| P-glycoprotein Substrate | Non-substrate | 0.6426 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8460 |
| Non-inhibitor | 0.8169 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8853 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.6168 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7985 |
| CYP450 2D6 Substrate | Non-substrate | 0.8648 |
| CYP450 3A4 Substrate | Non-substrate | 0.7037 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.8016 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9391 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9654 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9524 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9832 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8166 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7607 |
| Non-inhibitor | 0.8778 | |
| AMES Toxicity | Non AMES toxic | 0.9128 |
| Carcinogens | Carcinogens | 0.5710 |
| Fish Toxicity | High FHMT | 0.9621 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9998 |
| Honey Bee Toxicity | High HBT | 0.7388 |
| Biodegradation | Ready biodegradable | 0.6018 |
| Acute Oral Toxicity | III | 0.6225 |
| Carcinogenicity (Three-class) | Non-required | 0.7077 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.0622 | LogS |
| Caco-2 Permeability | 1.3687 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6468 | LD50, mol/kg |
| Fish Toxicity | -0.5750 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.3352 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty aldehydes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty aldehydes |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty aldehyde - Alpha-hydrogen aldehyde - 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 fatty aldehydes. These are long chain aldehydes with a chain of at least 12 carbon atoms. |
From ClassyFire