Armstrong's acid (naphthalene-1,5-disulfonic acid) is a fluorescent organic compound with the formula C10H6(SO3H)2. It is one of several isomers of naphthalenedisulfonic acid. It a colorless solid, typically obtained as the tetrahydrate.[1] Like other sulfonic acids, it is a strong acid. It is named for British chemist Henry Edward Armstrong.[2]
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Names | |||
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Preferred IUPAC name
Naphthalene-1,5-disulfonic acid | |||
Other names
Armstrong's acid
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Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.001.199 | ||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C10H8S2O6 | |||
Molar mass | 288.299 g/mol | ||
Appearance | colorless solid | ||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards
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corrosive | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Production and use
editIt is prepared by disulfonation of naphthalene with oleum:
- C10H8 + 2 SO3 → C10H6(SO3H)2
Further sulfonation gives The 1,3,5-trisulfonic acid derivative.[1]
Reactions and uses
editFusion of Armstrong's acid in NaOH gives the disodium salt of 1,5-dihydroxynaphthalene, which can be acidified to give the diol. The intermediate in this hydrolysis, 1-hydroxynaphthalene-5-sulfonic acid, is also useful. Nitration gives nitrodisulfonic acids, which are precursors to amino derivatives.
The disodium salt is sometimes used as a divalent counterion for forming salts of basic drug compounds, as an alternative to the related mesylate or tosylate salts. When used in this way such a salt is called a naphthalenedisulfonate salt, as seen with the most common salt form of the stimulant drug CFT. The disodium salt is also used as an electrolyte in certain kinds of chromatography.[3]
References
edit- ^ a b Gerald Booth "Naphthalene Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_009.
- ^ Senning, Alexander (2007). Elsevier's dictionary of chemoetymology. Elsevier. p. 30. ISBN 978-0-444-52239-9.
- ^ Shigeru Terabe "Electrokinetic chromatography: An interface between electrophoresis and chromatography" TrAC Trends in Analytical Chemistry 1989, Volume 8, pp. 129–134. doi:10.1016/0165-9936(89)85022-8