Iron(II) acetate
Names | |
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IUPAC name
Iron(II) acetate
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Other names
Ferrous acetate
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Identifiers | |
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3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.019.492 |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C4H6FeO4 | |
Molar mass | 173.933 g·mol−1 |
Appearance | White crystals (anhydrous) Light green crystals (tetrahydrate) |
Odor | Odorless |
Density | 1.734 g/cm3 (−73 °C)[1] |
Melting point | 190–200 °C (374–392 °F; 463–473 K) decomposes[2][3] |
Soluble[2] | |
Structure | |
Orthorhombic, oP75 (200 K) | |
Pbcn, No. 60 (200 K)[1] | |
2/m 2/m 2/m (200 K) | |
a = 18.1715(4) Å, b = 22.1453(5) Å, c = 8.2781(2) Å (200 K) α = 90°, β = 90°, γ = 90°
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Hazards | |
GHS labelling: | |
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Warning | |
H315, H319, H335[3] | |
P261, P305+P351+P338[3] | |
NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Iron(II) acetate describes compounds with formula Fe(CH3CO2)2·(H2O)x where x can be 0 (anhydrous) or 4 (tetrahydrate). The anhydrous compound is a white solid, although impure samples can be slightly colored.[1] The tetrahydrate is light green solid that is highly soluble in water.
Preparation and structure
[edit]Iron powder reacts with acetic acid to give the ferrous acetate, with evolution of hydrogen gas:[5][1]
- Fe + 2 CH3CO2H → Fe(CH3CO2)2 + H2
Reaction of scrap iron with acetic acid affords a brown mixture of various iron(II) and iron(III) acetates that are used in dyeing.[6]
It can also be made from the insoluble, olive green, Iron(II) carbonate.[citation needed]
It adopts a polymeric structure with octahedral Fe(II) centers interconnected by acetate ligands. It is a coordination polymer.[1]
Uses
[edit]Ferrous acetate is used as a mordant by the dye industry. Ebonizing wood is one such process.[7]
References
[edit]- ^ a b c d e f Weber, Birgit; Betz, Richard; Bauer, Wolfgang; Schlamp, Stephan (2011). "Crystal Structure of Iron(II) Acetate". Zeitschrift für anorganische und allgemeine Chemie. 637: 102–107. doi:10.1002/zaac.201000274.
- ^ a b Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. ISBN 978-1-4200-9084-0.
- ^ a b c d Sigma-Aldrich Co., Iron(II) acetate. Retrieved on 2014-05-03.
- ^ "MSDS of Ferrous acetate". fishersci.ca. Fair Lawn: Fisher Scientific. Retrieved 2014-08-02.
- ^ "Synthesis of Iron(II) acetate hydrate (ferrous acetate)". Archived from the original on 2013-08-25. Retrieved 2009-01-07.
- ^ Wildermuth, Egon; Stark, Hans; Friedrich, Gabriele; Ebenhöch, Franz Ludwig; Kühborth, Brigitte; Silver, Jack; Rituper, Rafael (2000). "Iron Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_591. ISBN 978-3527306732.
- ^ Ebonizing Wood with Ferric Acetate