POLYVINYLPYRROLIDONE
Relevant Data
Food Additives Approved in the United States
Food Additives Approved by European Union:
General Information
Synonyms: | POVIDONE, PVP |
Chemical Names: | POLYVINYLPYRROLIDONE; POLY [1-(2-OXO-1-PYRROLIDINYL)-ETHYLENE] |
CAS number: | 9003-39-8 |
INS: | 1201 |
Functional Class: |
Food Additives ADJUVANT EMULSIFIER STABILIZER THICKENER FILTERING_AID TABLETING_AID |
From apps.who.int
Evaluations
Evaluation year: | 1986 |
ADI: | 0-50 mg/kg bw |
Meeting: | 30 |
Specs Code: | R |
Report: | TRS 751-JECFA 30/30 |
Tox Monograph: | FAS 15-JECFA 24/127 (1980) |
Specification: | COMPENDIUM ADDENDUM 12/FNP 52 Add. 12/67 (METALS LIMITS) (2004). R; FAO JECFA Monographs 1 vol.3/105 |
From apps.who.int
GSFA Provisions for POLYVINYLPYRROLIDONE
Number | Food Category | Max Level | Notes |
---|---|---|---|
14.2.1 | Beer and malt beverages |
10 mg/kg | Note 36 |
14.2.2 | Cider and perry |
2 mg/kg | Note 36 |
From www.fao.org
Computed Descriptors
Download SDF2D Structure | |
CID | 6917 |
IUPAC Name | 1-ethenylpyrrolidin-2-one |
InChI | InChI=1S/C6H9NO/c1-2-7-5-3-4-6(7)8/h2H,1,3-5H2 |
InChI Key | WHNWPMSKXPGLAX-UHFFFAOYSA-N |
Canonical SMILES | C=CN1CCCC1=O |
Molecular Formula | (C6H9NO)n |
Wikipedia | Polyvinylpyrrolidone |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 111.144 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 1 |
Complexity | 120.0 |
CACTVS Substructure Key Fingerprint | A A A D c c B i I 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 A A A A A A A A A A A H g A A A A A A C A D B g A Q A A A M A A A C I A A E W U A A A A A A A A g A I A A E I A A A A A B A A g A A E A A A A B g C 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 = = |
Topological Polar Surface Area | 20.3 |
Monoisotopic Mass | 111.068 |
Exact Mass | 111.068 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 8 |
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+ | 0.9975 |
Human Intestinal Absorption | HIA+ | 0.9867 |
Caco-2 Permeability | Caco2+ | 0.6353 |
P-glycoprotein Substrate | Non-substrate | 0.7096 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.6767 |
Non-inhibitor | 0.9765 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.5195 |
Distribution | ||
Subcellular localization | Mitochondria | 0.5378 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8157 |
CYP450 2D6 Substrate | Non-substrate | 0.7679 |
CYP450 3A4 Substrate | Substrate | 0.5636 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.6533 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.6461 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8082 |
CYP450 2C19 Inhibitor | Inhibitor | 0.5089 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8954 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7806 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9078 |
Non-inhibitor | 0.9531 | |
AMES Toxicity | Non AMES toxic | 0.9133 |
Carcinogens | Non-carcinogens | 0.9309 |
Fish Toxicity | Low FHMT | 0.7704 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.7696 |
Honey Bee Toxicity | Low HBT | 0.6573 |
Biodegradation | Not ready biodegradable | 0.6941 |
Acute Oral Toxicity | III | 0.7900 |
Carcinogenicity (Three-class) | Warning | 0.5206 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.3963 | LogS |
Caco-2 Permeability | 1.5309 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.9102 | LD50, mol/kg |
Fish Toxicity | 1.5863 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -0.1015 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organoheterocyclic compounds |
Class | Pyrrolidines |
Subclass | Pyrrolidones |
Intermediate Tree Nodes | Not available |
Direct Parent | Pyrrolidine-2-ones |
Alternative Parents | |
Molecular Framework | Aliphatic heteromonocyclic compounds |
Substituents | 2-pyrrolidone - Tertiary carboxylic acid amide - Lactam - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteromonocyclic compound |
Description | This compound belongs to the class of organic compounds known as pyrrolidine-2-ones. These are pyrrolidines which bear a C=O group at position 2 of the pyrrolidine ring. |
From ClassyFire