2-Ethyl-6-methylpyrazine
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 2-Ethyl-6-methylpyrazine |
| CAS number | 13925-03-6 |
| COE number | 11331 |
| JECFA number | 769 |
| Flavouring type | substances |
| FL No. | 14.114 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | 95% (sum of 2,5- and 2,6-isomers); 60-63% 2,5-isomer and 30-35% 2,6-isomer |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 26332 |
| IUPAC Name | 2-ethyl-6-methylpyrazine |
| InChI | InChI=1S/C7H10N2/c1-3-7-5-8-4-6(2)9-7/h4-5H,3H2,1-2H3 |
| InChI Key | RAFHQTNQEZECFL-UHFFFAOYSA-N |
| Canonical SMILES | CCC1=NC(=CN=C1)C |
| Molecular Formula | C7H10N2 |
| Wikipedia | 2-ethyl-6-methylpyrazine |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 122.171 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Complexity | 83.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B j 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 s A A A A A A A A A A A B g A A A H A A A A A A A C A j B F g Q u g B I I E A C g A R R n R A A A g C Q x E i A A U A A 4 c A g A Y E B A g Q A U A A A A A A D A Q 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 = = |
| Topological Polar Surface Area | 25.8 |
| Monoisotopic Mass | 122.084 |
| Exact Mass | 122.084 |
| XLogP3 | None |
| XLogP3-AA | 1.0 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| 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+ | 0.9797 |
| Human Intestinal Absorption | HIA+ | 0.9784 |
| Caco-2 Permeability | Caco2+ | 0.6771 |
| P-glycoprotein Substrate | Non-substrate | 0.5984 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8922 |
| Non-inhibitor | 0.9972 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7931 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4906 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8808 |
| CYP450 2D6 Substrate | Non-substrate | 0.7716 |
| CYP450 3A4 Substrate | Non-substrate | 0.7646 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6661 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9649 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8854 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9395 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9552 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8795 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9601 |
| Non-inhibitor | 0.9183 | |
| AMES Toxicity | Non AMES toxic | 0.9236 |
| Carcinogens | Non-carcinogens | 0.8437 |
| Fish Toxicity | Low FHMT | 0.8622 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8759 |
| Honey Bee Toxicity | Low HBT | 0.6372 |
| Biodegradation | Not ready biodegradable | 0.9657 |
| Acute Oral Toxicity | III | 0.8454 |
| Carcinogenicity (Three-class) | Non-required | 0.6404 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.6273 | LogS |
| Caco-2 Permeability | 1.4723 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.1737 | LD50, mol/kg |
| Fish Toxicity | 2.4886 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.3102 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Diazines |
| Subclass | Pyrazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyrazines |
| Alternative Parents | |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyrazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as pyrazines. These are compounds containing a pyrazine ring, which is a six-member aromatic heterocycle, that consists of two nitrogen atoms (at positions 1 and 4) and four carbon atoms. |
From ClassyFire