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Salicylic acid is an organic compound with the formula HOC 6 H 4 COOH. [3] A colorless (or white), bitter-tasting solid, it is a precursor to and a metabolite of ...
Salicylic acid as a medication is used to help remove the outer layer of the skin. [1] As such it is used to treat warts, calluses, psoriasis, dandruff, acne, ringworm, and ichthyosis. [1] [2] Because of its effect on skin cells, salicylic acid is used in some shampoos to treat dandruff. [medical citation needed]
Methyl salicylate (oil of wintergreen or wintergreen oil) is an organic compound with the formula C 8 H 8 O 3.It is the methyl ester of salicylic acid.It is a colorless, viscous liquid with a sweet, fruity odor reminiscent of root beer (in which it is used as a flavoring), [4] but often associatively called "minty", as it is an ingredient in mint candies. [5]
Salicylic Acid Serum 2%. Calling all folks with sensitive skin: This one's for you.The 2 percent salicylic acid in this one is backed by maltobionic acid, a PHA that gently dissolves dead skin ...
There are typically two types of products: adhesive pads treated with salicylic acid or a bottle of concentrated salicylic acid. Removing a wart with this method requires a strict regimen of cleaning the area, applying the salicylic acid, and removing the dead skin with a pumice stone or emery board. It may take up to 12 weeks to remove a ...
A 12-week daily treatment with salicylic acid has been shown to lead to a complete clearance of warts in 10–15% of the cases. [16] Formic acid, topical, is a common treatment for plantar warts, which works by being applied over a period of time, causing the body to reject the wart. [17]
Salicylates are derivatives of salicylic acid that occur naturally in plants and serve as a natural immune hormone and preservative, protecting the plants against diseases, insects, fungi, and harmful bacteria. Salicylates can also be found in many medications, perfumes and preservatives. Both natural and synthetic salicylates can cause health ...
It is synthesized by heating salicylic acid with phenol in the presence of phosphoryl chloride. [4] It also arises from heating salicylic acid: [5] 2 HOC 6 H 4 CO 2 H → C 6 H 5 O 2 C 6 H 4 OH + CO 2 + H 2 O. The conversion entails dehydration and decarboxylation. Heating phenyl salicylate in turn gives xanthone. [6] [3]
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