| Names | |
|---|---|
Other names
| |
| Identifiers | |
| |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.034.612 |
| EC Number |
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| UNII | |
| UN number | 3077 |
| |
| |
| Properties | |
| C6H12FeN3O12 | |
| Molar mass | 374.016 g·mol−1 |
| Appearance | Green solid |
| Soluble | |
| Solubility inEthanol | Insoluble |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H302,H312,H315,H319,H332,H335 | |
| P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P312,P304+P340,P305+P351+P338,P312,P321,P322,P330,P332+P313,P337+P313,P362,P363,P403+P233,P405,P501 | |
| NFPA 704 (fire diamond) | |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Ferric ammonium oxalate (also known asammonium ferrioxalate orammonium tris(oxalato)ferrate) is theammonium salt of the anionic trisoxalatocoordination complex of iron(III). It is a precursor to iron oxides, diversecoordination polymers, andPrussian Blue.[1][2] The latter behavior is relevant to the manufacture ofblueprint paper. Ferric ammonium oxalate has also been used in the synthesis of superconducting salts with bis(ethylene)dithiotetrathiafulvalene (BEDT-TTF), seeOrganic superconductor.[3]