Poly(vinylpyrrolidone)-Iodine complex - 10mM in DMSO , CAS No.25655-41-8

CAS: 25655-41-8 Cat. No.: P422896 Summenformel: (C₆H₉NO)_n·xI EG-Nummer: 607-771-8

QUALITÄT & REINHEIT 10mM in DMSO

Synonyms

Povidone iodine|25655-41-8|Povidone-iodine|Betadine|Isodine|PVP iodine|PVP-I|PVP-Iodine|Isobetadyne|Bridine|Disphex|Povadyne|Ultradine|Efo-dine|1-ethenylpyrrolidin-2-one;molecular iodine|NSC26245|povidone.iodine|molecular iodine; 1-vinylpyrrolidin-2-one|1

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Spezifikationen

Synonyme

Povidone iodine | 25655-41-8 | Povidone-iodine | Betadine | Isodine | PVP iodine | PVP-I | PVP-Iodine | Isobetadyne | Bridine | Disphex | Povadyne | Ultradine | Efo-dine | 1-ethenylpyrrolidin-2-one;molecular iodine | NSC26245 | povidone.iodine | molecular iodine; 1-vinylpyrrolidin-2-one | 1

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

PVP-1 is used as a slow iodine release formulation that iodinates lipids and oxidizes cell compounds such as tyrosine sidechains. It is used as a carbon nanotube coating agent to improve water solubility.Universal antiseptic agent. Shows antibiotic effect

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

Pubchem Sid

528774810

Kanonisches Lächeln

C=CN1CCCC1=O.II

IUPAC Name

1-ethenylpyrrolidin-2-one;molecular iodine

InChIKey

CPKVUHPKYQGHMW-UHFFFAOYSA-N

INCHI

1S/C6H9NO.I2/c1-2-7-5-3-4-6(7)8;1-2/h2H,1,3-5H2;

Isomere SMILES

C=CN1CCCC1=O.II

WGK Deutschland

2

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Pyrrolidines
      • Subclass Pyrrolidones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Pyrrolidines
• Subclass: Pyrrolidones
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrrolidine-2-ones
• Alternative Parents: Tertiary carboxylic acid amides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• 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
• Beschreibung: 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.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Molekulargewicht: 364.950 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 364.877 Da
• Monoisotopic Mass: 364.877 Da
• Topological Polar Surface Area: 20.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 120.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3