General Information

MaintermTRIBUTYL PHOSPHATE
CAS Reg.No.(or other ID)126-73-8
Regnum 175.105
176.180
176.210

From www.fda.gov

Computed Descriptors

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2D Structure
CID31357
IUPAC Nametributyl phosphate
InChIInChI=1S/C12H27O4P/c1-4-7-10-14-17(13,15-11-8-5-2)16-12-9-6-3/h4-12H2,1-3H3
InChI KeySTCOOQWBFONSKY-UHFFFAOYSA-N
Canonical SMILESCCCCOP(=O)(OCCCC)OCCCC
Molecular FormulaC12H27O4P
Wikipediatri-N-butyl phosphate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight266.318
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count12
Complexity175.0
CACTVS Substructure Key Fingerprint A A A D c e B w O A 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 G g A A A C A A C A C g g A I C A A A A A R A A Q A A A A 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 E 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 = =
Topological Polar Surface Area44.8
Monoisotopic Mass266.165
Exact Mass266.165
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count17
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+0.9540
Human Intestinal AbsorptionHIA+0.9646
Caco-2 PermeabilityCaco2+0.5183
P-glycoprotein SubstrateNon-substrate0.7196
P-glycoprotein InhibitorNon-inhibitor0.7677
Non-inhibitor0.9143
Renal Organic Cation TransporterNon-inhibitor0.9096
Distribution
Subcellular localizationMitochondria0.6359
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8593
CYP450 2D6 SubstrateNon-substrate0.8348
CYP450 3A4 SubstrateNon-substrate0.5380
CYP450 1A2 InhibitorNon-inhibitor0.8922
CYP450 2C9 InhibitorNon-inhibitor0.8767
CYP450 2D6 InhibitorNon-inhibitor0.9352
CYP450 2C19 InhibitorNon-inhibitor0.8655
CYP450 3A4 InhibitorNon-inhibitor0.8952
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9058
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.7082
Non-inhibitor0.9017
AMES ToxicityNon AMES toxic0.9610
CarcinogensCarcinogens 0.7021
Fish ToxicityHigh FHMT0.7423
Tetrahymena Pyriformis ToxicityHigh TPT0.9851
Honey Bee ToxicityHigh HBT0.8751
BiodegradationNot ready biodegradable0.7319
Acute Oral ToxicityIII0.8339
Carcinogenicity (Three-class)Non-required0.4754

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.4750LogS
Caco-2 Permeability0.5235LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.9166LD50, mol/kg
Fish Toxicity1.0701pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.2897pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassOrganic phosphoric acids and derivatives
SubclassPhosphate esters
Intermediate Tree NodesAlkyl phosphates
Direct ParentTrialkyl phosphates
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsTrialkyl phosphate - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as trialkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly three alkyl chains.

From ClassyFire