| Identification | Back Directory | [Name]
URANYL NITRATE | [CAS]
10102-06-4 | [Synonyms]
D014502
UO2(NO3)2
URANYL NITRATE
Nitrate, uranyl
Nitrate, uranium
Uranyl dinitrate
URANYL(2+)NITRATE,SOLID
Uranium, bis(nitrato-o)dioxo-, (T-4)-
Uranyl nitrate (solid): (Bis(nitrato-O,O')dioxouranium) | [Molecular Formula]
N2O8U | [MDL Number]
MFCD00036300 | [MOL File]
10102-06-4.mol | [Molecular Weight]
394.04 |
| Chemical Properties | Back Directory | [Melting point ]
60.2°C | [Boiling point ]
118°C | [density ]
2.807 | [solubility ]
soluble in ethyl ether | [form ]
yellow-green solid | [color ]
yellow crystals, crystalline | [Water Solubility ]
127@25 | [Uses]
Uranyl nitrate is a yellow poisonous crystal made by dissolving
uranic oxide in nitric acid. It is soluble in water, alcohol, and
ether. First suggested by C. J. Burnett in 1855, a uranyl nitrate
printing process was patented by Niépce de St. Victor in 1858.
The paper was floated on a uranyl nitrate solution and dried
in the dark. The paper was exposed under a negative in the
sun until a faint image appeared. The image was developed to
completion by floating the paper on a solution of silver nitrate
or gold chloride followed by washing. A process patented in
1864 by Jacob Wothly called for adding uranyl nitrate and
silver to collodion, which was then applied to paper. The
Wothlytype was a printing-out process.
Uranyl nitrate was used in printing-out emulsions and with
potassium ferricyanide for toning prints and intensifying negatives.
It was also used with silver nitrate for making uranium/
silver gaslight papers. | [EPA Substance Registry System]
Uranyl nitrate (10102-06-4) |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow, rhombic crystals. Soluble in water, alcohol, and
ether. | [Uses]
Source of uranium dioxide, extraction of uranium
into nonaqueous solvents. | [Hazard]
Strong oxidizer. Corrosive and irritating. | [Physical properties]
The hexahydrate is a yellow crystalline solid; orthogonal crystals; density 2.81 g/cm3; hygroscopic; melts at 60°C; decomposes at 118°C; very soluble in water; soluble in alcohol and ether. | [Preparation]
Uranyl nitrate is obtained as an intermediate in recovering uranium from its minerals. The compound can be prepared by reacting triuranium octaoxide, U3O8, with nitric acid. It is separated and purified by extraction with ether. |
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