2-METHYL-2-BUTENAL
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | 2,3-DIMETHYLACROLEIN, 2-METHYLCROTONALDEHYDE, TIGLALDEHYDE |
| Chemical Names: | 2-METHYL-2-BUTENAL |
| CAS number: | 1115-11-3 |
| JECFA number: | 1201 |
| FEMA number: | 3407 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2003 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 922-JECFA 61/75 |
| Tox Monograph: | FAS 52-JECFA 61/289 |
| Specification: | COMPENDIUM ADDENDUM 11/FNP 52 Add. 11/109 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5321950 |
| IUPAC Name | (E)-2-methylbut-2-enal |
| InChI | InChI=1S/C5H8O/c1-3-5(2)4-6/h3-4H,1-2H3/b5-3+ |
| InChI Key | ACWQBUSCFPJUPN-HWKANZROSA-N |
| Canonical SMILES | CC=C(C)C=O |
| Molecular Formula | C5H8O |
| Wikipedia | Trans-2-Methyl-2-butenal |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 84.118 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Complexity | 72.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 D A C g g A I C A A A A A A C I A i h S g A A A A A A A A A A A C A E A A E A A A A A A A Q A A A A A A A A A A A Y 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 | 17.1 |
| Monoisotopic Mass | 84.058 |
| Exact Mass | 84.058 |
| XLogP3 | None |
| XLogP3-AA | 0.9 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 6 |
| 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+ | 0.9416 |
| Human Intestinal Absorption | HIA+ | 0.9951 |
| Caco-2 Permeability | Caco2+ | 0.7581 |
| P-glycoprotein Substrate | Non-substrate | 0.7518 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8927 |
| Non-inhibitor | 0.9737 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9133 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.3980 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8435 |
| CYP450 2D6 Substrate | Non-substrate | 0.9310 |
| CYP450 3A4 Substrate | Non-substrate | 0.6970 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8650 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9375 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9318 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9000 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9562 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7792 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9281 |
| Non-inhibitor | 0.9713 | |
| AMES Toxicity | Non AMES toxic | 0.7383 |
| Carcinogens | Carcinogens | 0.7133 |
| Fish Toxicity | High FHMT | 0.5170 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9373 |
| Honey Bee Toxicity | High HBT | 0.8700 |
| Biodegradation | Ready biodegradable | 0.7830 |
| Acute Oral Toxicity | III | 0.8030 |
| Carcinogenicity (Three-class) | Non-required | 0.5968 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.3653 | LogS |
| Caco-2 Permeability | 1.6724 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7823 | LD50, mol/kg |
| Fish Toxicity | 0.6200 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.0291 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Alpha,beta-unsaturated carbonyl compounds - Alpha,beta-unsaturated aldehydes |
| Direct Parent | Enals |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Enal - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Aldehyde - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as enals. These are an alpha,beta-unsaturated aldehyde of general formula RC=C-CH=O in which the aldehydic C=O function is conjugated to a C=C triple bond at the alpha,beta position. |
From ClassyFire