TRIBUTYL PHOSPHATE
General Information
Mainterm | TRIBUTYL PHOSPHATE |
CAS Reg.No.(or other ID) | 126-73-8 |
Regnum |
175.105 176.180 176.210 |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 31357 |
IUPAC Name | tributyl phosphate |
InChI | InChI=1S/C12H27O4P/c1-4-7-10-14-17(13,15-11-8-5-2)16-12-9-6-3/h4-12H2,1-3H3 |
InChI Key | STCOOQWBFONSKY-UHFFFAOYSA-N |
Canonical SMILES | CCCCOP(=O)(OCCCC)OCCCC |
Molecular Formula | C12H27O4P |
Wikipedia | tri-N-butyl phosphate |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 266.318 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 12 |
Complexity | 175.0 |
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 Area | 44.8 |
Monoisotopic Mass | 266.165 |
Exact Mass | 266.165 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 17 |
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+ | 0.9540 |
Human Intestinal Absorption | HIA+ | 0.9646 |
Caco-2 Permeability | Caco2+ | 0.5183 |
P-glycoprotein Substrate | Non-substrate | 0.7196 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.7677 |
Non-inhibitor | 0.9143 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.9096 |
Distribution | ||
Subcellular localization | Mitochondria | 0.6359 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8593 |
CYP450 2D6 Substrate | Non-substrate | 0.8348 |
CYP450 3A4 Substrate | Non-substrate | 0.5380 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.8922 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8767 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9352 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.8655 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8952 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9058 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7082 |
Non-inhibitor | 0.9017 | |
AMES Toxicity | Non AMES toxic | 0.9610 |
Carcinogens | Carcinogens | 0.7021 |
Fish Toxicity | High FHMT | 0.7423 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9851 |
Honey Bee Toxicity | High HBT | 0.8751 |
Biodegradation | Not ready biodegradable | 0.7319 |
Acute Oral Toxicity | III | 0.8339 |
Carcinogenicity (Three-class) | Non-required | 0.4754 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.4750 | LogS |
Caco-2 Permeability | 0.5235 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.9166 | LD50, mol/kg |
Fish Toxicity | 1.0701 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.2897 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic acids and derivatives |
Class | Organic phosphoric acids and derivatives |
Subclass | Phosphate esters |
Intermediate Tree Nodes | Alkyl phosphates |
Direct Parent | Trialkyl phosphates |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Trialkyl phosphate - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aliphatic acyclic compound |
Description | This 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