Basic information
- Standard SMILES
C=CN1CCCC1=O.II- InChIKey
FAAHNQAYWKTLFD-UHFFFAOYSA-N- Molecular formula
- C6H9I2NO
- Average molar mass
- 364.95 g/mol
Overview
See also: Isopropanol (annotation moved to); Povidone-Iodine (annotation moved to).
Names & identifiers
- Preferred name
- Efo-dine
- IUPAC
- 1-ethenylpyrrolidin-2-one;molecular iodine
- English name
- Povidone iodine
- Molecular formula
- C6H9I2NO
- Molecular weight
- 364.95
Names & synonyms
Show more names
Database identifiers
- CAS
25655-41-8- PubChem CID
- 410087
- ChEMBL
CHEMBL5424182
Properties
Computed structural properties
- Topological polar surface area
- 20.3 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 1
- Heavy atoms
- 10
- Formal charge
- 0
- Complexity
- 120
Physicochemical properties
- Melting point
- 300 °C · 300 °C
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- 2 O: · H2O: soluble100mg/mL
- form
- Powder
- color
- Yellow-brown
- Odor
- ylsh. brn. amorphous powd., sl. char. odor
- Water Solubility
- Soluble in water, ethyl alcohol, isopropyl alcohol, polyethylene glycol and glycerol. Insoluble in chloroform, carbon tetrachloride, hexane, acetone and petroleum ether.
- Merck
- 13 · 13,7784
- Cosmetics Ingredients Functions
- ANTIMICROBIAL
- InChI
- InChI=1S/C6H9NO.I2/c1-2-7-5-3-4-6(7)8;1-2/h2H,1,3-5H2;
- InChIKey
- FAAHNQAYWKTLFD-UHFFFAOYSA-N
- SMILES
- II.C(N1CCCC1=O)=C
- CAS DataBase Reference
- 25655 · 25655-41-8(CAS DataBase Reference)
- FDA 21 CFR
- 310.545 · 310.545
- EWG's Food Scores
- 1 · 1-3
- FDA UNII
- 85 H0HZU99M · 85H0HZU99M
- NCI Drug Dictionary
- Betadine
- ATC code
- 8 AG02,D09AA09,D11AC06,G01AX11,R02AA15,S01AX18 · D08AG02,D09AA09,D11AC06,G01AX11,R02AA15,S01AX18
- EPA Substance Registry System
- Povidone-iodine (25655-41-8)
- UNSPSC Code
- 51102829 · 51102829
- NACRES
- 85 · NA.85
- Symbol(GHS)
- 5 · GHS05,GHS09
- Signal word
- Danger
- Hazard statements
- 315 · H315-H318-H411
- Precautionary statements
- 264 · P264-P273-P280-P302+P352-P305+P351+P338-P332+P313
- PPE
- 95 · Eyeshields, Gloves, type N95 (US)
- Safety Statements
- 24 · 24/25-22
- WGK Germany
- 2 · 2
- RTECS
- 1579600 · TR1579600
- TSCA
- TSCA listed
- HS Code
- 29339900 · 29339900
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 Eye · Aquatic Chronic 2Eye Dam. 1Skin Irrit. 2
- Hazardous Substances Data
- 25655 · 25655-41-8(Hazardous Substances Data)
Safety & regulation
Safety data
- PPE
- Eyeshields, Gloves, type N95 (US)
- wgk
- 2
- tsca
- TSCA listed
- rtecs
- TR1579600
- hs_code
- 29339900
- Signal word
- Danger
- Symbol(GHS)
- GHS05,GHS09
- safety_code
- 24/25-22
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H318-H411
- Hazard Classifications
- Aquatic Chronic 2Eye Dam. 1Skin Irrit. 2
- Precautionary statements
- P264-P273-P280-P302+P352-P305+P351+P338-P332+P313
- Hazardous Substances Data
- 25655-41-8(Hazardous Substances Data)
Chemistry & industry
Applications
Usespovidone iodine has bactericidal effect like iodine. It can be used as disinfectant and bacteriostatic agent in the medicine for anti-septic purposes for eye drops, nasal drops, and cream agents. It can also be made into disinfectant. povidone iodine is mainly used for the skin disinfection and equipment disinfection in hospital surgery and injections as well as prevention of infection in the field of stomatology, gynecology, surgery, and dermatology; it can also be used for disinfection of household utensils and appliances; for food industry and aquaculture industry, it is used for disinfection and animal disease control. It is the preferred international and domestic choice of medical iodine-contained fungicides and disinfectants for epidemic prevention. povidone iodine is a kind of iodine carrier, the so-called “tamed iodine”. Because this product can gradually release iodine to exert an antibacterial effect; its mechanism of action is through causing the protein denaturation and further death of bacteria. It is effective in treating bacteria, fungi, as well as viruses with a relative small tissue irritation effect.
DescriptionPovidone iodine is iodophor, used as topical antiseptic in surgery and for skin and mucous membrane infections, also as aerosol. A 10% povidone iodine solution contains 1% available iodine, but free-iodine is at 0.1% concentration. Skin exposure causes irritant rather than allergic contact dermatitis. In such a situation, however, iodine seems to be the true hapten.
HistoryPovidone iodine (PI) is frequently used during surgical preparation, postoperative wound cleaning and dressing. It was described by Shelaski about seventy years ago (Shelanski and Shelanski, 1956). PI consists of the complex structure of povidone, a polymer that is structurally similar to plasma proteins, and the iodine element, which has antimicrobial properties. The function of polyvinylpyrrolidone (PVP) used as a polymer includes increasing iodine solubility and penetration, decreasing iodine ion concentration and keeping iodine bound. However, PVP does not have antimicrobial properties. Shelanski defined this complex structure as 'iodophor' (Shelanski and Shelanski, 1956).
Preparation methods
PreparationPovidone Iodine Solution is an antiseptic and disinfectant agent. The preparation method of povidone iodine: be that 1.17% potassium iodide is dissolved in part water in 10% water by mass percent, 2.34% iodine is added to wherein stirring and dissolving, be mixed with iodine solution standby; 0.01% stability auxiliary agent is dissolved in part water 10% water standby; In complex reaction still, add remaining water, open and stir, dropping into 10.0% polyvinylpyrrolidone k30 dissolves, then substep adds above-mentioned two kinds of solution that prepare, finally add 7.5% solvent normal propyl alcohol, after feeding intake, allow reactant mixture at 20 ℃, react 2 hours, react complete mixture is lowered the temperature and obtained betagen solution.
Upstream & downstream products
Upstream raw materials
Suppliers50 total
Related reactions
No reaction records under the current filter.
Linked notes
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