3,4-Dimethylcyclopentan-1,2-dione
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 3,4-Dimethylcyclopentan-1,2-dione |
| CAS number | 13494-06-9 |
| COE number | 2234 |
| JECFA number | 420 |
| Flavouring type | substances |
| FL No. | 07.075 |
| 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 | 61633 |
| IUPAC Name | 3,4-dimethylcyclopentane-1,2-dione |
| InChI | InChI=1S/C7H10O2/c1-4-3-6(8)7(9)5(4)2/h4-5H,3H2,1-2H3 |
| InChI Key | WGAVDEVFJDQIMZ-UHFFFAOYSA-N |
| Canonical SMILES | CC1CC(=O)C(=O)C1C |
| Molecular Formula | C7H10O2 |
| Wikipedia | 3,4-dimethyl 1,2-cyclopentandione |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 126.155 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Complexity | 160.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g M A A A A A A A A A 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 G g A A A A A A D Q S A g A A C A A A A A A A I A I A Q A A A A A A A A A A A A A A E A A A A A A B I A A A A A A A A A A A A A A A E I i g A O g A A A A A A A A A A A A A A A A A A A A A A A C A A A A A = = |
| Topological Polar Surface Area | 34.1 |
| Monoisotopic Mass | 126.068 |
| Exact Mass | 126.068 |
| XLogP3 | None |
| XLogP3-AA | 0.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| 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+ | 0.9893 |
| Human Intestinal Absorption | HIA+ | 0.9962 |
| Caco-2 Permeability | Caco2+ | 0.7119 |
| P-glycoprotein Substrate | Non-substrate | 0.7710 |
| P-glycoprotein Inhibitor | Inhibitor | 0.5540 |
| Non-inhibitor | 0.9731 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8858 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6905 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8536 |
| CYP450 2D6 Substrate | Non-substrate | 0.8576 |
| CYP450 3A4 Substrate | Non-substrate | 0.5627 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8279 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9476 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9225 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9375 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9746 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9779 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9728 |
| Non-inhibitor | 0.9278 | |
| AMES Toxicity | Non AMES toxic | 0.8973 |
| Carcinogens | Non-carcinogens | 0.7514 |
| Fish Toxicity | Low FHMT | 0.6603 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.7182 |
| Honey Bee Toxicity | High HBT | 0.6958 |
| Biodegradation | Ready biodegradable | 0.8047 |
| Acute Oral Toxicity | III | 0.6954 |
| Carcinogenicity (Three-class) | Non-required | 0.6297 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.0612 | LogS |
| Caco-2 Permeability | 1.3734 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7946 | LD50, mol/kg |
| Fish Toxicity | 2.6124 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.9081 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones |
| Direct Parent | Cyclic ketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Cyclic ketone - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety. |
From ClassyFire