| Weight | 177.03 g/mol |
|---|---|
| Formula | C7H6Cl2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,4-Dichlorobenzyl alcohol (1777-82-8)
dichlorobenzyl alcohol
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- Randomised, Double-Blind, Placebo-Controlled Study of a Single Dose of an Amylmetacresol/2,4-dichlorobenzyl Alcohol Plus Lidocaine Lozenge or a Hexylresorcinol Lozenge for the Treatment of Acute Sore Throat Due to Upper Respiratory Tract Infection (Journal of Pharmacy and Pharmaceutical Sciences, 2012)
- 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, 2005)
- The internal barriers to rotation about the carboncarbon bond in 3,5-dichlorobenzyl alcohol and selenol by the J method (Canadian Journal of Chemistry, 1978)
- Evaluation of the antimicrobial effects of sodium benzoate and dichlorobenzyl alcohol against dental plaque microorganisms: An in vitro study (Acta Odontologica Scandinavica, 1994)
- FT-Raman and FT-IR spectra, ab initio and density functional studies of 3,4-dichlorobenzyl alcohol (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2006)
- Copper(II) complexes with 4-amino--(t-butylaminomethyl)-3,5-dichlorobenzyl alcohol hydrochloride (Clenbuterol). Crystal structures of the binuclear and mononuclear Cu(II) complexes with Clenbuterol (Polyhedron, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dichlorobenzyl alcohol
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SMILESC1=CC(=C(C=C1Cl)Cl)CO
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InChIKeyDBHODFSFBXJZNY-UHFFFAOYSA-N
- Pubchem - 2,4-Dichlorobenzyl alcohol
- Wikipedia - dichlorobenzyl alcohol
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 Strepsils, Lorsept, and Gorpils. A low-pH throat lozenge containing dichlorobenzyl alcohol (1.2mg) and amylmetacresol (0.6mg) has been found to deactivate respiratory syncytial virus and SARS-Cov, but not adenovirus or rhinovirus.
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