Relevant Data

Food Additives Approved by WHO:

Food Additives Approved by European Union:

  • Butylated hydroxyanisole (BHA) [show]

General Information

Computed Descriptors

Download SDF
2D Structure
CID8456
IUPAC Name2-tert-butyl-4-methoxyphenol
InChIInChI=1S/C11H16O2/c1-11(2,3)9-7-8(13-4)5-6-10(9)12/h5-7,12H,1-4H3
InChI KeyMRBKEAMVRSLQPH-UHFFFAOYSA-N
Canonical SMILESCC(C)(C)C1=C(C=CC(=C1)OC)O
Molecular FormulaC11H16O2
Wikipedia3-tert-butyl-4-hydroxyanisole

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight180.247
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Complexity160.0
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 g S A m A I y B o A A B g C A A i B C A A A C C A A g I A A I i A A G C I g M J i K G M R q A c C A k w B E I u A f A w P A P g Q A B A A A I A A A C A A I A A B A A A A A A A A A A A A = =
Topological Polar Surface Area29.5
Monoisotopic Mass180.115
Exact Mass180.115
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count13
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+0.9007
Human Intestinal AbsorptionHIA+0.9903
Caco-2 PermeabilityCaco2+0.8864
P-glycoprotein SubstrateNon-substrate0.6469
P-glycoprotein InhibitorNon-inhibitor0.8490
Non-inhibitor0.9368
Renal Organic Cation TransporterNon-inhibitor0.8889
Distribution
Subcellular localizationMitochondria0.9024
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7671
CYP450 2D6 SubstrateNon-substrate0.5652
CYP450 3A4 SubstrateSubstrate0.5541
CYP450 1A2 InhibitorInhibitor0.5624
CYP450 2C9 InhibitorNon-inhibitor0.9200
CYP450 2D6 InhibitorNon-inhibitor0.9142
CYP450 2C19 InhibitorNon-inhibitor0.7903
CYP450 3A4 InhibitorNon-inhibitor0.8145
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7835
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9511
Non-inhibitor0.9225
AMES ToxicityNon AMES toxic0.9344
CarcinogensNon-carcinogens0.7320
Fish ToxicityHigh FHMT0.5200
Tetrahymena Pyriformis ToxicityHigh TPT0.7314
Honey Bee ToxicityHigh HBT0.8658
BiodegradationNot ready biodegradable0.8871
Acute Oral ToxicityIII0.8429
Carcinogenicity (Three-class)Non-required0.6353

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.9751LogS
Caco-2 Permeability1.6943LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.8232LD50, mol/kg
Fish Toxicity0.4143pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.2241pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassBenzenoids
ClassPhenols
SubclassMethoxyphenols
Intermediate Tree NodesNot available
Direct ParentMethoxyphenols
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsMethoxyphenol - 4-alkoxyphenol - Phenylpropane - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

From ClassyFire