Armstrong acid
Chemical compound
From Wikipedia, the free encyclopedia
Armstrong 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 | |||
| Identifiers | |||
3D model (JSmol) |
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| 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 |
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
Reactions and uses
Fusion of Armstrong 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]

