DIISOAMYL DISULFIDE
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | DIISOAMYL DISULFIDE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 2051-04-9 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 74915 |
| IUPAC Name | 3-methyl-1-(3-methylbutyldisulfanyl)butane |
| InChI | InChI=1S/C10H22S2/c1-9(2)5-7-11-12-8-6-10(3)4/h9-10H,5-8H2,1-4H3 |
| InChI Key | MPYGLNNTOXLWOB-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CCSSCCC(C)C |
| Molecular Formula | C10H22S2 |
| Wikipedia | diisoamyl disulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 206.406 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 7 |
| Complexity | 77.8 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w A A B g 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 A Q A A A A A D Q C E Q A C 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 A A A A A A A A A A A A A A A A A A A A A A A A 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 = = |
| Topological Polar Surface Area | 50.6 |
| Monoisotopic Mass | 206.116 |
| Exact Mass | 206.116 |
| XLogP3 | None |
| XLogP3-AA | 4.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9701 |
| Human Intestinal Absorption | HIA+ | 0.9952 |
| Caco-2 Permeability | Caco2+ | 0.6208 |
| P-glycoprotein Substrate | Non-substrate | 0.6601 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8911 |
| Non-inhibitor | 0.9100 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8299 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.4916 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8473 |
| CYP450 2D6 Substrate | Non-substrate | 0.7860 |
| CYP450 3A4 Substrate | Non-substrate | 0.6633 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8054 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8521 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8780 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8480 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9041 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8378 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7959 |
| Non-inhibitor | 0.8744 | |
| AMES Toxicity | Non AMES toxic | 0.8622 |
| Carcinogens | Carcinogens | 0.6905 |
| Fish Toxicity | High FHMT | 0.9900 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9950 |
| Honey Bee Toxicity | High HBT | 0.8326 |
| Biodegradation | Not ready biodegradable | 0.9257 |
| Acute Oral Toxicity | III | 0.7741 |
| Carcinogenicity (Three-class) | Non-required | 0.6093 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -5.0657 | LogS |
| Caco-2 Permeability | 1.3931 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.1829 | LD50, mol/kg |
| Fish Toxicity | 0.0939 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.1339 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Organic disulfides |
| Subclass | Dialkyldisulfides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkyldisulfides |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkyldisulfide - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as dialkyldisulfides. These are organic compounds containing a disulfide group R-SS-R' where R and R' are both alkyl groups. |
From ClassyFire