Octenidine dihydrochloride
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Names | |
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IUPAC name
N-octyl-1-[10-(4-octyliminopyridin-1-yl)decyl]pyridin-4-imine dihydrochloride
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Systematic IUPAC name
N,N'-(decane-1,10-diyldipyridin-1-yl-4-ylidene)dioctan-1-amine dihydrochloride
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Other names
N,N'-(decane-1,10-diyldi-1(4H)-pyridyl-4-ylidene)bis(octylammonium) dichloride
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Identifiers | |
70775-75-6 71251-02-00 |
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ChEBI | CHEBI:478961 |
ChemSpider | 46370 |
EC Number | 274-861-8 |
Jmol 3D model | Interactive image |
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Properties | |
C36H64Cl2N4 | |
Molar mass | 623.84 g·mol−1 |
Pharmacology | |
ATC code | R02 combination codes: D08AJ57 G01AX66 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Octenidine dihydrochloride is a cationic surfactant, with a bolaamphiphile structure, derived from pyridine. It is primarily used as an antiseptic
Contents
Use
Since 1987, octenidine is being used in Europe as an antiseptic, in concentrations of 0.1-2.0%. It is a substitute for chlorhexidine, with respect to its slow action and concerns about the carcinogenic impurity 4-chloroaniline. Octenidine antiseptics often contain phenoxyethanol.
Efficacy
Effective concentration, % | ||
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Octenidine dihydrochloride | Chlorhexidine digluconate | |
Staphylococcus aureus | 0.025 | >0.2 |
Escherichia coli | 0.025 | 0.1 |
Proteus mirabilis | 0.025 | >0.2 |
Pseudomonas aeruginosa | 0.025 | >0.2 |
Candida albicans | 0.01 | 0.025 |
Safety
Octenidine is absorbed neither through the skin nor through mucous membranes nor via wounds and does not pass the placental barrier. However, cation-active compounds cause local irritation and are extremely poisonous when administered parenterally.[2] Wound irrigation with octenidine caused severe complications in dogs.[3]
References
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- Antiseptics
- Imines
- Pyridines
- Chlorides
- Quaternary ammonium compounds
- Cationic surfactants
- Organic chemistry stubs