Relevant Data

Flavouring Substances Approved by European Union:

  • Pentyl salicylate [show]

General Information

MaintermAMYL SALICYLATE
Doc TypeNIL
CAS Reg.No.(or other ID)2050-08-0
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID16299
IUPAC Namepentyl 2-hydroxybenzoate
InChIInChI=1S/C12H16O3/c1-2-3-6-9-15-12(14)10-7-4-5-8-11(10)13/h4-5,7-8,13H,2-3,6,9H2,1H3
InChI KeyRANVDUNFZBMTBK-UHFFFAOYSA-N
Canonical SMILESCCCCCOC(=O)C1=CC=CC=C1O
Molecular FormulaC12H16O3
Wikipediaamyl salicylate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight208.257
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Complexity191.0
CACTVS Substructure Key Fingerprint A A A D c e B w 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 G g A A C A A A D A S g m A I y D o A A B g C I A i D S C A A C A A A k I A A I i A E G C M g I J z a C N R q C c U A l 4 B E I u Y e I y C C O A A A A A A A I A A A A A A A A A B A A A A A A A A A A A A = =
Topological Polar Surface Area46.5
Monoisotopic Mass208.11
Exact Mass208.11
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count15
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8808
Human Intestinal AbsorptionHIA+0.9954
Caco-2 PermeabilityCaco2+0.8119
P-glycoprotein SubstrateSubstrate0.5164
P-glycoprotein InhibitorNon-inhibitor0.8334
Non-inhibitor0.9495
Renal Organic Cation TransporterNon-inhibitor0.8161
Distribution
Subcellular localizationMitochondria0.8943
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7822
CYP450 2D6 SubstrateNon-substrate0.8472
CYP450 3A4 SubstrateNon-substrate0.5666
CYP450 1A2 InhibitorInhibitor0.7528
CYP450 2C9 InhibitorNon-inhibitor0.7889
CYP450 2D6 InhibitorNon-inhibitor0.8580
CYP450 2C19 InhibitorInhibitor0.7044
CYP450 3A4 InhibitorNon-inhibitor0.9244
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7842
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8865
Non-inhibitor0.7730
AMES ToxicityNon AMES toxic0.9367
CarcinogensNon-carcinogens0.8526
Fish ToxicityHigh FHMT0.9299
Tetrahymena Pyriformis ToxicityHigh TPT0.9876
Honey Bee ToxicityHigh HBT0.6654
BiodegradationReady biodegradable0.8029
Acute Oral ToxicityIII0.8472
Carcinogenicity (Three-class)Non-required0.6050

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.3664LogS
Caco-2 Permeability1.1936LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.9119LD50, mol/kg
Fish Toxicity0.5544pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.8856pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree NodesBenzoic acid esters
Direct Parento-Hydroxybenzoic acid esters
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsO-hydroxybenzoic acid ester - Salicylic acid or derivatives - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous acid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.

From ClassyFire