Tripropylamine
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Tripropylamine |
| CAS number | 102-69-2 |
| COE number | 10495 |
| JECFA number | 1612 |
| Flavouring type | substances |
| FL No. | 11.026 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7616 |
| IUPAC Name | N,N-dipropylpropan-1-amine |
| InChI | InChI=1S/C9H21N/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3 |
| InChI Key | YFTHZRPMJXBUME-UHFFFAOYSA-N |
| Canonical SMILES | CCCN(CCC)CCC |
| Molecular Formula | C9H21N |
| Wikipedia | tri-N-propylamine |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 143.274 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 6 |
| Complexity | 47.5 |
| CACTVS Substructure Key Fingerprint | A A A D c e B y 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 A A H A A A A A A A C A D B A A Q C A A 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 I A A A A A A A A A A A E A A A A A A C 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 | 3.2 |
| Monoisotopic Mass | 143.167 |
| Exact Mass | 143.167 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9515 |
| Human Intestinal Absorption | HIA+ | 0.9783 |
| Caco-2 Permeability | Caco2+ | 0.7606 |
| P-glycoprotein Substrate | Non-substrate | 0.5842 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8165 |
| Non-inhibitor | 0.7698 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.6090 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.7643 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8705 |
| CYP450 2D6 Substrate | Non-substrate | 0.5884 |
| CYP450 3A4 Substrate | Non-substrate | 0.6290 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5343 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9501 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8475 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8802 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9545 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8854 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.5000 |
| Non-inhibitor | 0.6160 | |
| AMES Toxicity | Non AMES toxic | 0.9589 |
| Carcinogens | Carcinogens | 0.7432 |
| Fish Toxicity | High FHMT | 0.5246 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.6069 |
| Honey Bee Toxicity | Low HBT | 0.5000 |
| Biodegradation | Not ready biodegradable | 0.7803 |
| Acute Oral Toxicity | II | 0.7377 |
| Carcinogenicity (Three-class) | Non-required | 0.5304 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.3427 | LogS |
| Caco-2 Permeability | 1.2135 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 3.1254 | LD50, mol/kg |
| Fish Toxicity | 1.8319 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3510 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Tertiary amines |
| Direct Parent | Trialkylamines |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen. |
From ClassyFire