Dimethyl succinate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Dimethyl succinate |
| CAS number | 106-65-0 |
| COE number | 439 |
| JECFA number | 616 |
| Flavouring type | substances |
| FL No. | 09.445 |
| 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 | 7820 |
| IUPAC Name | dimethyl butanedioate |
| InChI | InChI=1S/C6H10O4/c1-9-5(7)3-4-6(8)10-2/h3-4H2,1-2H3 |
| InChI Key | MUXOBHXGJLMRAB-UHFFFAOYSA-N |
| Canonical SMILES | COC(=O)CCC(=O)OC |
| Molecular Formula | C6H10O4 |
| Wikipedia | dimethyl succinate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 146.142 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Complexity | 114.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g 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 A A A A A A A A A A A A A G g A A A A A A C A C A g A I C C A A A B A A I A A C Q C A A A A A A A A A A A A A E A A A A A A B A A A A A A A A A E A A A A A A B D 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 | 52.6 |
| Monoisotopic Mass | 146.058 |
| Exact Mass | 146.058 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9785 |
| Human Intestinal Absorption | HIA+ | 0.7244 |
| Caco-2 Permeability | Caco2+ | 0.6156 |
| P-glycoprotein Substrate | Non-substrate | 0.7388 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9022 |
| Non-inhibitor | 0.8730 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8980 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8034 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8364 |
| CYP450 2D6 Substrate | Non-substrate | 0.9036 |
| CYP450 3A4 Substrate | Non-substrate | 0.6118 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.9208 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9470 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9644 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9584 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9786 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9555 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9507 |
| Non-inhibitor | 0.9661 | |
| AMES Toxicity | Non AMES toxic | 0.9156 |
| Carcinogens | Non-carcinogens | 0.6400 |
| Fish Toxicity | High FHMT | 0.6100 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.8703 |
| Honey Bee Toxicity | High HBT | 0.7380 |
| Biodegradation | Ready biodegradable | 0.8909 |
| Acute Oral Toxicity | III | 0.8726 |
| Carcinogenicity (Three-class) | Non-required | 0.8027 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.1344 | LogS |
| Caco-2 Permeability | 0.6810 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4344 | LD50, mol/kg |
| Fish Toxicity | 0.9195 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.0449 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid methyl esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid methyl ester - Dicarboxylic acid or derivatives - Methyl ester - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acid methyl esters. These are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group. |
From ClassyFire