Home  

Random  

Nearby  



Log in  



Settings  



Donate  



About Wikipedia  

Disclaimers  



Wikipedia





Ammonium iron(II) sulfate





Article  

Talk  



Language  

Watch  

Edit  





Ammonium iron(II) sulfate, or Mohr's salt, is the inorganic compound with the formula (NH4)2SO4.Fe(SO4).6H2O. Containing two different cations, Fe2+ and NH+4, it is classified as a double saltofferrous sulfate and ammonium sulfate. It is a common laboratory reagent because it is readily crystallized, and crystals resist oxidation by air. Like the other ferrous sulfate salts, ferrous ammonium sulfate dissolves in water to give the aquo complex [Fe(H2O)6]2+, which has octahedral molecular geometry.[1] Its mineral form is mohrite.

Ammonium iron(II) sulfate
Names
IUPAC name

Ammonium iron(II) sulfate

Other names

Ferrous ammonium sulfate
Ammonium iron sulfate
Mohr's salt

Identifiers

CAS Number

  • hexahydrate: 7783-85-9
  • 3D model (JSmol)

    ChEBI
  • hexahydrate: CHEBI:76181 checkY
  • ChemSpider
  • hexahydrate: 13084980 checkY
  • ECHA InfoCard 100.030.125 Edit this at Wikidata
    EC Number
    • 233-151-8

    PubChem CID

  • hexahydrate: 15942308
  • UNII
  • hexahydrate: 99A04ICQ3J
  • CompTox Dashboard (EPA)

    • InChI=1S/Fe.2H3N.2H2O4S/c;;;2*1-5(2,3)4/h;2*1H3;2*(H2,1,2,3,4)/q+2;;;;/p-2 checkY

      Key: IMBKASBLAKCLEM-UHFFFAOYSA-L checkY

    • InChI=1/Fe.2H3N.2H2O4S/c;;;2*1-5(2,3)4/h;2*1H3;2*(H2,1,2,3,4)/q+2;;;;/p-2

      Key: IMBKASBLAKCLEM-NUQVWONBAX

    • [Fe+2].[O-]S(=O)(=O)[O-].[O-]S([O-])(=O)=O.[NH4+].[NH4+]

    Properties

    Chemical formula

    Fe(SO4)(NH4)2(SO4) (anhydrous)
    Fe(SO4)(NH4)2(SO4)·6H2O (hexahydrate)
    Molar mass 284.05 g mol−1 (anhydrous)
    392.14 g mol−1 (hexahydrate)
    Appearance Blue-green solid
    Density 1.86 g/cm3
    Melting point 100 to 110 °C (212 to 230 °F; 373 to 383 K)
    Boiling point Not applicable

    Solubility in water

    269 g/L (hexahydrate)
    Hazards
    GHS labelling:

    Pictograms

    GHS07: Exclamation mark

    Signal word

    Warning

    Hazard statements

    H315, H319, H335

    Precautionary statements

    P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
    NFPA 704 (fire diamond)
    NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
    2
    0
    0
    Safety data sheet (SDS) Fisher MSDS
    Related compounds

    Related compounds

    Ammonium iron(III) sulfate

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Structure

    edit

    This compound is a member of a group of double sulfates called Schönites or Tutton's salts. Tutton's salts form monoclinic crystals and have formula M2N(SO4)2·6H2O (M = various monocations). With regards to the bonding, crystals consist of octahedra [Fe(H2O)6]2+ centers, which are hydrogen bonded to sulfate and ammonium.[2]

     
    Structure of ferrous ammonium sulfate with hydrogen bonding network highlighted (N is violet, O is red; S is orange, Fe is light red).

    Mohr's salt is named after the German chemist Karl Friedrich Mohr, who made many important advances in the methodology of titration in the 19th century.

    Applications

    edit

    Inanalytical chemistry, this salt is the preferred source of ferrous ions as the solid has a long shelf life, being resistant to oxidation. This stability extends somewhat to solutions reflecting the effect of pH on the ferrous–ferric redox couple. This oxidation occurs more readily at high pH. The ammonium ions make solutions of Mohr's salt slightly acidic, which slows this oxidation process.[1][3] Sulfuric acid is commonly added to solutions to reduce oxidation to ferric iron.

    It is used in the Fricke's dosimeter to measure high doses of gamma rays.[4]

    Preparation

    edit

    Mohr's salt forms upon evaporation of an equimolar mixture of aqueous ferrous sulfate and ammonium sulfate.[5]

    Contaminants

    edit

    Common impurities include magnesium, nickel, manganese, lead, and zinc, many of which form isomorphous salts.[6]

    References

    edit
    1. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • ^ Ephraim, Fritz (1926). Inorganic Chemistry. tr P. C. L. Thorne. London: Gurney and Jackson. pp. 484–485.
  • ^ "Ammonium Ferrous Sulphate 100 g (Mohr's Salt)". 2012. Retrieved 13 June 2013.
  • ^ Hickman, C.; Lorrain, S.; Barthe, J.R.; Portal, G. (1986). "Use of Mohr's Salt for High Level Gamma Dosimetry (Up to 108Gy)". Radiation Protection Dosimetry. 17 (1–4). Oxford Journals: 255–257. doi:10.1093/oxfordjournals.rpd.a079818.
  • ^ Wildermuth, Egon; Stark, Hans; Friedrich, Gabriele; Ebenhöch, Franz Ludwig; Kühborth, Brigitte; Silver, Jack; Rituper, Rafael (2000). "Iron Compounds". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a14_591. ISBN 978-3-527-30385-4.
  • ^ Vogel, Arthur I. (1961). A Text-book of Quantitative Inorganic Analysis Including Elementary Instrumental Analysis (3 ed.). Longmans. pp. 281–282.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Ammonium_iron(II)_sulfate&oldid=1226210844"
     



    Last edited on 29 May 2024, at 06:38  





    Languages

     


    العربية
    تۆرکجه
    Català
    Чӑвашла
    Čeština
    Deutsch
    Español
    Esperanto
    فارسی
    Français
    Bahasa Indonesia
    Italiano
    Latviešu
    Magyar
    Nederlands

    Occitan
    Polski
    Português
    Русский
    Slovenščina
    Српски / srpski
    Srpskohrvatski / српскохрватски
    Suomi
    Svenska
    ி
    Українська

     

    Wikipedia


    This page was last edited on 29 May 2024, at 06:38 (UTC).

    Content is available under CC BY-SA 4.0 unless otherwise noted.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Terms of Use

    Desktop