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  2. 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.

  3. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    The United States Drug Enforcement Administration (DEA) maintains lists regarding the classification of illicit drugs (see DEA Schedules).It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs.

  4. 3-Nitrobenzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/3-nitrobenzyl_alcohol

    Other names m-Nitrobenzyl alcohol Benzyl alcohol, m-nitro 3-Nitrobenzyl alcohol Benzenemethanol, 3-nitro-3-Nitrobenzenemethanol. Identifiers CAS Number.

  5. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    Like other types of phenols, they are slowly oxidized by exposure to air, and the resulting impurities often give the samples a yellow to brownish red tint. Cresols have an odor characteristic to that of other simple phenols, reminiscent to some of a "coal tar" smell. The name "cresol" is an adduct of phenol and their traditional source, creosote.

  6. 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 ...

  7. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...

  8. Benzyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_benzoate

    It is also used in other animals; however, it is considered toxic to cats. [1] How it works is unclear. [5] Benzyl benzoate was first studied medically in 1918. [1] It is on the World Health Organization's List of Essential Medicines. [6] Benzyl benzoate is sold under the brand name Scabanca among others and is available as a generic medication.

  9. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

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