Names | |
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Other names
cupferron
ammonium N-nitrosophenylhydroxylamine | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.004.713 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C6H9N3O2 | |
Molar mass | 155.157 g·mol−1 |
Melting point | 150 to 155 °C (302 to 311 °F; 423 to 428 K) |
Soluble | |
Hazards | |
GHS labelling: | |
Danger | |
H301, H315, H319, H335, H351 | |
P201, P202, P261, P264, P270, P271, P280, P281, P301+P310, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cupferron is jargon for the ammonium salt of the conjugate base derived from N-nitroso-N-phenylhydroxylamine. It once was a common reagent for the complexation of metal ions, being of interest in the area of qualitative inorganic analysis. Its formula is NH4[C6H5N(O)NO]. The anion binds to metal cations through the two oxygen atoms, forming five-membered chelate rings.