3,7-DIMETHYLOCTANAL
Relevant Data
Food Additives Approved by WHO:
General Information
Mainterm | 3,7-DIMETHYLOCTANAL |
Doc Type | EAF |
CAS Reg.No.(or other ID) | 5988-91-0 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 110747 |
IUPAC Name | 3,7-dimethyloctanal |
InChI | InChI=1S/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h8-10H,4-7H2,1-3H3 |
InChI Key | UCSIFMPORANABL-UHFFFAOYSA-N |
Canonical SMILES | CC(C)CCCC(C)CC=O |
Molecular Formula | C10H20O |
Wikipedia | 3,7-dimethyloctanal |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 156.269 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 6 |
Complexity | 97.0 |
CACTVS Substructure Key Fingerprint | A A A D c e B w 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 Q C g g A I C A A A A A A A I A A g Q g 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 M C 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 = = |
Topological Polar Surface Area | 17.1 |
Monoisotopic Mass | 156.151 |
Exact Mass | 156.151 |
XLogP3 | None |
XLogP3-AA | 3.4 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 11 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
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+ | 0.9855 |
Human Intestinal Absorption | HIA+ | 0.9879 |
Caco-2 Permeability | Caco2+ | 0.7878 |
P-glycoprotein Substrate | Non-substrate | 0.6848 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.8868 |
Non-inhibitor | 0.7761 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8868 |
Distribution | ||
Subcellular localization | Mitochondria | 0.4564 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8168 |
CYP450 2D6 Substrate | Non-substrate | 0.8338 |
CYP450 3A4 Substrate | Non-substrate | 0.5959 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.6565 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9361 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9707 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9618 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9858 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9447 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8615 |
Non-inhibitor | 0.8406 | |
AMES Toxicity | Non AMES toxic | 0.9426 |
Carcinogens | Carcinogens | 0.6098 |
Fish Toxicity | High FHMT | 0.9392 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9966 |
Honey Bee Toxicity | High HBT | 0.7366 |
Biodegradation | Ready biodegradable | 0.5363 |
Acute Oral Toxicity | III | 0.8417 |
Carcinogenicity (Three-class) | Non-required | 0.7450 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -3.5895 | LogS |
Caco-2 Permeability | 1.3336 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.4678 | LD50, mol/kg |
Fish Toxicity | 0.0784 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.7503 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic oxygen compounds |
Class | Organooxygen compounds |
Subclass | Carbonyl compounds |
Intermediate Tree Nodes | Aldehydes |
Direct Parent | Medium-chain aldehydes |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Medium-chain aldehyde - Alpha-hydrogen aldehyde - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
Description | This compound belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms. |
From ClassyFire