ISOBUTYL N-METHYLANTHRANILATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Chemical Names: | 2-METHYLPROPYL N-METHYL-2-AMINOBENZOATE |
| CAS number: | 65505-24-0 |
| COE number: | 9769 |
| JECFA number: | 1548 |
| FEMA number: | 4149 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2008 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Meeting: | 69 |
| Specs Code: | S |
| Report: | TRS 934-JECFA 65/54 |
| Tox Monograph: | FAS 56-JECFA 65 |
| Specification: | FAO JECFA Monographs 5/137 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 522171 |
| IUPAC Name | 2-methylpropyl 2-(methylamino)benzoate |
| InChI | InChI=1S/C12H17NO2/c1-9(2)8-15-12(14)10-6-4-5-7-11(10)13-3/h4-7,9,13H,8H2,1-3H3 |
| InChI Key | WKYZGTHZBSYUFI-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)COC(=O)C1=CC=CC=C1NC |
| Molecular Formula | C12H17NO2 |
| Wikipedia | isobutyl N-methylanthranilate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 207.273 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Complexity | 204.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B y M 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 w A A A A A A A A A A A B A A A A H g A Q A A A A D Q i h m A Y y y I L A B A C I A i T S S A C C A A A l A g A I i I E I b M g I J j r A t Z m G M Y h m 0 A F I 6 c e Y y C C O A A A A A A A C A A A A A A A A A A Q A A A A A A A A A A A = = |
| Topological Polar Surface Area | 38.3 |
| Monoisotopic Mass | 207.126 |
| Exact Mass | 207.126 |
| XLogP3 | None |
| XLogP3-AA | 3.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| 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+ | 0.9425 |
| Human Intestinal Absorption | HIA+ | 0.9833 |
| Caco-2 Permeability | Caco2+ | 0.8004 |
| P-glycoprotein Substrate | Non-substrate | 0.8391 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7558 |
| Non-inhibitor | 0.7913 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8709 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8557 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7815 |
| CYP450 2D6 Substrate | Non-substrate | 0.7260 |
| CYP450 3A4 Substrate | Non-substrate | 0.5396 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.7149 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8230 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8532 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8556 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9255 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6067 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9635 |
| Non-inhibitor | 0.9306 | |
| AMES Toxicity | Non AMES toxic | 0.9397 |
| Carcinogens | Non-carcinogens | 0.6289 |
| Fish Toxicity | High FHMT | 0.9751 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9591 |
| Honey Bee Toxicity | Low HBT | 0.5719 |
| Biodegradation | Ready biodegradable | 0.5000 |
| Acute Oral Toxicity | III | 0.7787 |
| Carcinogenicity (Three-class) | Non-required | 0.5670 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.8186 | LogS |
| Caco-2 Permeability | 1.8546 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9868 | LD50, mol/kg |
| Fish Toxicity | 0.5207 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7167 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acid esters |
| Alternative Parents |
|
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aminobenzoic acid or derivatives - Benzoate ester - Benzoyl - Aniline or substituted anilines - Phenylalkylamine - Secondary aliphatic/aromatic amine - Vinylogous amide - Amino acid or derivatives - Carboxylic acid ester - Secondary amine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Amine - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. |
From ClassyFire