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Salicyclic acid

Catalog No. DB00936 Name DrugBank
CAS Number 69-72-7 Website http://www.ualberta.ca/
M. F. C7H6O3 Telephone (780) 492-3111
M. W. 138.12074 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 812

SYNONYMS

IUPAC name
2-hydroxybenzoic acid
IUPAC Traditional name
salicyclic acid
Brand Name
Rutranex
Ionil
Dr. Scholl's Wart Remover Kit
Salicylic acid soap
Duoplant
Advanced pain relief corn removers
Duofil Wart Remover
Keralyt
Kyselina 2-hydroxybenzoova
Kyselina salicylova
Psoriacid-s-stift
SAX
Saligel
Advanced pain relief callus removers
Clear away wart remover
Compound W
Dr. Scholl's Callus Removers
Dr. Scholl's Corn Removers
Freezone
Retarder SAX
Retarder W
Salicylic acid collodion
Salonil
Stri-dex
Synonyms
2-Hydroxybenzoic acid
O-carboxyphenol
SA
Salicylate
Salicylic acid
2-Carboxyphenol
2-Hydroxybenzenecarboxylic acid
Acido salicilico
O-hydroxybenzoic acid
Orthohydroxybenzoic acid
Phenol-2-carboxylic acid

DATABASE IDS

PubChem CID 338
CAS Number 69-72-7
PubChem SID 46504942

PROPERTIES

Hydrophobicity(logP) 2.4
Solubility 2.24 mg/mL at 25 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]

DETAILS

Description (English)
Item Information
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
Wikipedia

REFERENCES

  • 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
  • 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