DL-Isoborneol
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | DL-Isoborneol |
| CAS number | 124-76-5 |
| COE number | 2020 |
| JECFA number | 1386 |
| Flavouring type | substances |
| FL No. | 02.059 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | At least 92%; secondary component 3-5% borneol |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61060 |
| IUPAC Name | (1S,3R,4R)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-ol |
| InChI | InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10-/m0/s1 |
| InChI Key | DTGKSKDOIYIVQL-XKSSXDPKSA-N |
| Canonical SMILES | CC1(C2CCC1(C(C2)O)C)C |
| Molecular Formula | C10H18O |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 154.253 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Complexity | 185.0 |
| 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 Y M A A A A w A A A A A A A A A A A A A A A A G g A A C A A A D x S g g A I C A A A A A 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 E A I A A A A A Q A A E A A A A A A G A w P A P g A A A A A A A A A C A A A I A A B A A A Y A A D A A A A A = = |
| Topological Polar Surface Area | 20.2 |
| Monoisotopic Mass | 154.136 |
| Exact Mass | 154.136 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 3 |
| 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+ | 0.9793 |
| Human Intestinal Absorption | HIA+ | 0.9942 |
| Caco-2 Permeability | Caco2+ | 0.8073 |
| P-glycoprotein Substrate | Substrate | 0.5000 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7748 |
| Non-inhibitor | 0.9565 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8592 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.5234 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7913 |
| CYP450 2D6 Substrate | Non-substrate | 0.8494 |
| CYP450 3A4 Substrate | Substrate | 0.6872 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7344 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7997 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9696 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9001 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9495 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9602 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9299 |
| Non-inhibitor | 0.8000 | |
| AMES Toxicity | Non AMES toxic | 0.9133 |
| Carcinogens | Non-carcinogens | 0.8585 |
| Fish Toxicity | High FHMT | 0.8387 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8456 |
| Honey Bee Toxicity | High HBT | 0.8021 |
| Biodegradation | Not ready biodegradable | 0.7697 |
| Acute Oral Toxicity | III | 0.8105 |
| Carcinogenicity (Three-class) | Non-required | 0.6665 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.3826 | LogS |
| Caco-2 Permeability | 1.5714 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8269 | LD50, mol/kg |
| Fish Toxicity | 1.6756 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.6184 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bicyclic monoterpenoids |
| Alternative Parents | |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Bicyclic monoterpenoid - Bornane monoterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. |
From ClassyFire