Chemistry:2,4-Dichlorobenzyl alcohol
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Names | |
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Preferred IUPAC name
(2,4-Dichlorophenyl)methanol | |
Other names
Dybenal
Rapidosept Myacide SP | |
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Properties | |
C7H6Cl2O | |
Molar mass | 177.02 g·mol−1 |
Melting point | 57 to 60 °C (135 to 140 °F; 330 to 333 K) |
Boiling point | 150 °C (302 °F; 423 K) 25 mmHg |
Pharmacology | |
1=ATC code }} | R02AA03 (WHO) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
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2,4-Dichlorobenzyl alcohol is a mild antiseptic, able to kill bacteria and viruses associated with mouth and throat infections. It is a common ingredient in throat lozenges such as Cofsils, Strepsils, Lorsept, and Gorpils. It is also an ingredient in the European product Neo Borocillina.[1] A low-pH throat lozenge containing dichlorobenzyl alcohol (1.2 mg) and amylmetacresol (0.6 mg) has been found to deactivate respiratory syncytial virus and SARS-Cov, but not adenovirus or rhinovirus.[2] A dentifrice containing 10% sodium benzoate and 0.3% dichlorobenzyl alcohol maintains antimicrobial activity for 5 to 10 minutes after brushing.[3]
References
- ↑ "Neo Borocillina". drugs.com. https://www.drugs.com/international/neo-borocillina.html.
- ↑ "A throat lozenge containing amyl meta cresol and dichlorobenzyl alcohol has a direct virucidal effect on respiratory syncytial virus, influenza A and SARS-CoV". Antiviral Chemistry & Chemotherapy 16 (2): 129–34. 2005. doi:10.1177/095632020501600205. PMID 15889535.
- ↑ Ostergaard E (1994). "Evaluation of the antimicrobial effects of sodium benzoate and dichlorobenzyl alcohol against dental plaque microorganisms. An in vitro study.". Acta Odontol Scand 52 (6): 335–45. doi:10.3109/00016359409029031. PMID 7887143.
Original source: https://en.wikipedia.org/wiki/2,4-Dichlorobenzyl alcohol.
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