Nitrosylsulfuric acid
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| Nitrosylsulfuric acid | |
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Nitrosylsulfuric acid |
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Other names
nitrosonium bisulfate, chamber crystals |
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| Identifiers | |
| CAS number | 7782-78-7 |
| PubChem | 82157 |
| ChemSpider | 74147 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | HNO5S |
| Molar mass | 127.08 g/mol |
| Appearance | pale yellow crystals |
| Density | 1.612 g/mL in 40% sulfuric acid soln |
| Melting point |
73.5 °C |
| Boiling point |
decomposes |
| Solubility in water | decomposes |
| Solubility | soluble in H2SO4 |
| Hazards | |
| Main hazards | oxidizer |
| Related compounds | |
| Other anions | NOCl |
| Other cations | NaHSO4 |
| Related compounds | NOBF4 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Nitrosylsulfuric acid is the chemical compound with the formula NOHSO4.
This salt is a source of the NO+ ion, It can also be viewed as the mixed acid anhydride of sulfuric acid and nitrous acid:
- HNO2 + H2SO4 → NOHSO4 +H2O
NOHSO4 is useful in organic chemistry to prepare diazonium salts from amines. A typical procedure entails dissolving sodium nitrite in concentrated sulfuric acid in an ice bath.[1][2]
Related NO-delivery reagents include nitrosonium tetrafluoroborate, [NO]BF4, and nitrosyl chloride.
[edit] References
- ^ Hodgson, H, H.; Mahadevan, A. P. Ward, E. R. (1955), "1,4-Dinitronaphthalene", Org. Synth., http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv3p0341; Coll. Vol. 3: 341 (diazodization followed by treatment with nitrite)
- ^ Sandin, R. B.; Cairns, T. L. (1943), "1,2,3-Triiodo-5-nitrobenzene", Org. Synth., http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv2p0604; Coll. Vol. 2: 604 (diazodization followed by treatment with iodide)
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