Benzethonium chloride
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Names | |
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Preferred IUPAC name
N-Benzyl-N,N-dimethyl-2-{2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy}ethanaminium chloride
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Systematic IUPAC name
Benzyldimethyl(2-{2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy}ethyl)azanium chloride
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Identifiers | |
121-54-0 ![]() |
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3898548 | |
ChEBI | CHEBI:31264 ![]() |
ChEMBL | ChEMBL221753 ![]() |
ChemSpider | 8165 ![]() |
EC Number | 204-479-9 |
Jmol 3D model | Interactive image Interactive image |
KEGG | D01140 ![]() |
MeSH | Benzethonium |
PubChem | 8478 |
RTECS number | BO7175000 |
UNII | PH41D05744 ![]() |
UN number | 2923 |
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Properties | |
C27H42ClNO2 | |
Molar mass | 448.09 g·mol−1 |
Melting point | 163 °C (325 °F; 436 K) |
40 g dm−3 (at 20 °C) | |
Pharmacology | |
ATC code | D08 R02AA09 |
Legal status |
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topical | |
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 | |
Benzethonium chloride, also known as hyamine is a synthetic quaternary ammonium salt. This compound is an odorless white solid, soluble in water. It has surfactant, antiseptic, and anti-infective properties, and it is used as a topical antimicrobial agent in first aid antiseptics. It is also found in cosmetics and toiletries such as mouthwashes, anti-itch ointments, and antibacterial moist towelettes. Benzethonium chloride is also used in the food industry as a hard surface disinfectant.[1]
Uses
Antimicrobial
Benzethonium chloride exhibits a broad spectrum of microbiocidal activity against bacteria, fungi, mold and viruses. Independent testing shows that benzethonium chloride is highly effective against such pathogens as methicillin-resistant Staphylococcus aureus, Salmonella, Escherichia coli, Clostridium difficile, hepatitis B virus, hepatitis C virus, herpes simplex virus (HSV), human immunodeficiency virus (HIV), respiratory syncytial virus (RSV), and norovirus.[citation needed]
The US Food and Drug Administration (FDA) specifies that the safe and effective concentrations for benzethonium chloride are 0.1-0.2% in first aid products.[2] Aqueous solutions of benzethonium chloride are not absorbed through the skin. It is not approved in the US and Europe for use as a food additive. Being a quaternary ammonium salt, it is more toxic than negatively charged surfactants.[3] However, in a two-year study on rats, there was no evidence of carcinogenic activity.[4]
It is available under trade names Salanine, BZT, Diapp, Quatrachlor, Polymine D, Phemithyn, Antiseptol, Disilyn, Phermerol, and others.[5] It is also found in several grapefruit seed extract preparations[6] and can be used as a preservative, such as in the anaesthetic Ketamine.[7]
Other uses
In addition to its highly effective antimicrobial activity, benzethonium chloride contains a positively charged nitrogen atom covalently bonded to four carbon atoms. This positive charge attracts it to the skin and hair. This contributes to a soft, powdery afterfeel on the skin and hair, as well as long-lasting persistent activity against microorganisms. Also, this positively charged hydrophilic part of the molecule makes it a cationic detergent.[8]
Benzethonium chloride is also used to titrate the quantity of sodium dodecyl sulfate in a mixture of sodium dodecyl sulfate, sodium chloride and sodium sulfate, using dimidium bromide-sulphan blue as an indicator.[9]
References
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- ↑ Record in the Household Products Database of NLM
- ↑ Tentative final monograph (21CFR 333)
- ↑ Data Sheets
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Sciencelab.com, Benzethonium chloride MSDS
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- ↑ TOXNET
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