Substance

ID:814

Names and Identifiers
Synonyms
2-Hydroxybenzoic acidSASalicylic acidSalicyclic acidOrthohydroxybenzoic acid2-CarboxyphenolO-hydroxybenzoic acidPhenol-2-carboxylic acidO-carboxyphenolSalicylate2-Hydroxybenzenecarboxylic acidAcido salicilico
IUPAC Traditional name
salicyclic acid
IUPAC name
2-hydroxybenzoic acid
Brand Name
Dr. Scholl's Callus RemoversFreezoneKyselina 2-hydroxybenzoovaSAXStri-dexClear away wart removerCompound WSalicylic acid collodionSalicylic acid soapAdvanced pain relief corn removersDuoplantIonilKyselina salicylovaRetarder SAXSaligelSalonilDr. Scholl's Corn RemoversDr. Scholl's Wart Remover KitPsoriacid-s-stiftDuofil Wart RemoverKeralytRetarder WRutranexAdvanced pain relief callus removers
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Solubility
2.24 mg/mL at 25 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
Hydrophobicity(logP)
2.4
Molecule Details
Drug Groups
approved
Description
A compound obtained from the bark of the white willow and wintergreen leaves, and also prepared synthetically. It has bacteriostatic, fungicidal, and keratolytic actions. Its salts, the salicylates, are used as analgesics.
Indication
Key additive in many skin-care products for the treatment of acne, psoriasis, callouses, corns, keratosis pilaris and warts.
Pharmacology
Salicylic acid treats acne by causing skin cells to slough off more readily, preventing pores from clogging up. This effect on skin cells also makes salicylic acid an active ingredient in several shampoos meant to treat dandruff. Use of straight salicylic solution may cause hyperpigmentation on unpretreated skin for those with darker skin types (Fitzpatrick phototypes IV, V, VI), as well as with the lack of use of a broad spectrum sunblock. Subsalicylate in combination with bismuth form the popular stomach relief aid known commonly as Pepto-Bismol. When combined the two key ingredients help control diarrhea, nausea, heartburn, and even gas. It is also very mildly anti-biotic.
Toxicity
Oral rat LD50: 891 mg/kg. Inhalation rat LC50: > 900 mg/m3/1hr. Irritation: skin rabbit: 500 mg/24H mild. Eye rabbit: 100 mg severe. Investigated a mutagen and reproductive effector.
Affected Organisms
Humans and other mammals
References
• Vane JR: Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs. Nat New Biol. 1971 Jun 23;231(25):232-5. [Pubmed]
• Flower R, Gryglewski R, Herbaczynska-Cedro K, Vane JR: Effects of anti-inflammatory drugs on prostaglandin biosynthesis. Nat New Biol. 1972 Jul 26;238(82):104-6. [Pubmed]
External Links
Molecular Spectra
No Data Available
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References
• Vane JR: Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs. Nat New Biol. 1971 Jun 23;231(25):232-5. Pubmed
• Flower R, Gryglewski R, Herbaczynska-Cedro K, Vane JR: Effects of anti-inflammatory drugs on prostaglandin biosynthesis. Nat New Biol. 1972 Jul 26;238(82):104-6. Pubmed