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  2. 2,4-Dichlorobenzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorobenzyl_alcohol

    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 ...

  3. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  4. Amylmetacresol - Wikipedia

    en.wikipedia.org/wiki/Amylmetacresol

    Hypersensitivity reactions are very rare and show symptoms such as nausea or dyspepsia, although it is not entirely clear which side effects are caused by AMC and which by dichlorobenzyl alcohol or other ingredients of the lozenges. [1] [3] AMC has a low toxicity with an LD 50 of 1500 mg/kg body weight (in rats). [3] [6]

  5. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is used effectively for treating lice infestations as the active ingredient in lotion shampoo with 5% benzyl alcohol. [ 13 ] Benzyl alcohol is an ingredient used in the manufacture of soaps, topical creams, skin lotions, shampoos, and facial cleansers and is popular due to its anti-bacterial and anti-fungal properties.

  6. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups. [3] [4]

  7. 3,5-Dinitrobenzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/3,5-Dinitrobenzoyl_chloride

    3,5-Dinitrobenzoyl chloride (C 7 H 3 ClN 2 O 5) is an organic compound with a melting point of 68–69 °C. [1] It is the acyl chloride of 3,5-dinitrobenzoic acid and like it is mainly used in the analysis of organic substances by derivatization .

  8. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

    This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2. Ethanol; C3. 1-Propanol; Isopropyl alcohol; C4 n-Butanol; Isobutanol; sec-Butanol ...

  9. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...