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Salicylamide

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Salicylamide
Clinical data
MedlinePlusa681004
ATC code
Pharmacokinetic data
ExcretionRenal
Identifiers
  • 2-Hydroxybenzamide
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
NIAID ChemDB
CompTox Dashboard(EPA)
ECHA InfoCard100.000.554Edit this at Wikidata
Chemical and physical data
FormulaC7H7NO2
Molar mass137.138 g·mol−1
3D model (JSmol)
Density1.33 g/cm3
Solubility in waterSoluble in hot water, ether, alcohol, and chloroform. mg/mL (20 °C)
  • O=C(c1ccccc1O)N
  • InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10) checkY
  • Key:SKZKKFZAGNVIMN-UHFFFAOYSA-N checkY
  (verify)

Salicylamide (o-hydroxybenzamide oramide of salicyl) is a non-prescriptiondrug withanalgesic andantipyretic properties.[1] Its medicinal uses are similar to those ofaspirin.[2] Salicylamide is used in combination with bothaspirin andcaffeine in theover-the-counter pain remedy PainAid. It was also an ingredient in the over-the-counter pain remedyBC Powder but was removed from the formulation in 2009, andExcedrin used the ingredient from1960 to 1980 in conjunction withaspirin,acetaminophen, andcaffeine. It was used in later formulations ofVincent's powders in Australia as a substitute forphenacetin.

Pure salicylamide is a white or slightly pink crystalline powder

Derivatives

[edit]

Derivatives of salicylamide includeethenzamide,labetalol,medroxalol,otilonium,oxyclozanide,salicylanilide,niclosamide, andraclopride.

See also

[edit]

References

[edit]
  1. ^Borne R, Levi M, Wilson N (2008)."Nonsteroidal Anti-Inflammatory Drugs". In Foye WO, Williams DA (eds.).Foye's Principles of Medicinal Chemistry (6th ed.). Philadelphia London: Lippincott Williams & Wilkins. p. 968.ISBN 978-0-7817-6879-5.
  2. ^"Salicylamide". Dictionary.com. Merriam-Webster's Medical Dictionary. Merriam-Webster, Inc. RetrievedDecember 31, 2006.

External links

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