215406

Sigma-Aldrich

Ammonium iron(II) sulfate hexahydrate

ACS reagent, 99%

Synonym(s):
Mohr’s salt, Ammonium iron(II) sulfate, Ammonium ferrous sulfate hexahydrate
Linear Formula:
(NH4)2Fe(SO4)2 · 6H2O
CAS Number:
Molecular Weight:
392.14
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NB.24

Quality Level

grade

ACS reagent

assay

98.5-101.5%
99%

form

powder or crystals

reaction suitability

reagent type: catalyst
core: iron

impurities

≤0.01% insolubles
≤0.05% Not NH4OH pptd.

pH

3-5 (20 °C, 50 g/L)

mp

100 °C (dec.) (lit.)

anion traces

phosphate (PO43-): ≤0.003%

cation traces

Ca: 0.005%
Cu: ≤0.003%
Fe3+: ≤0.01%
K: 0.002%
Mg: 0.002%
Mn: ≤0.01%
Na: 0.02%
Zn: ≤0.003%

SMILES string

N.N.O.O.O.O.O.O.[Fe++].OS([O-])(=O)=O.OS([O-])(=O)=O

InChI

1S/Fe.2H3N.2H2O4S.6H2O/c;;;2*1-5(2,3)4;;;;;;/h;2*1H3;2*(H2,1,2,3,4);6*1H2/q+2;;;;;;;;;;/p-2

InChI key

MQLVWQSVRZVNIP-UHFFFAOYSA-L

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Target Organs

Respiratory system

WGK Germany

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

Konstantinos Grintzalis et al.
Free radical biology & medicine, 59, 27-35 (2012-10-09)
A simple and sensitive method is presented for the simultaneous quantification (spectrophotometric and spectrofluorimetric) of the main lipid and protein peroxidation products after their initial fractionation: free malondialdehyde (FrMDA), protein-bound malondialdehyde (PrMDA), total hydroperoxides (LOOH), and protein hydroperoxides (PrOOH). FrMDA...
Metallization of biologically inspired silica nanotubes.
Jo W, et al.
Materials Science and Engineering, C, 32(8), 2426-2430 (2012)
Mixed ligand complexes of iron (II) and (III) with cyanide and aromatic di-imines.
Schilt AA.
Journal of the American Chemical Society, 82(12), 3000-3005 (1960)
The crystal structure of Tutton's salts. VI. Vanadium (II), iron (II) and cobalt (II) ammonium sulfate hexahydrates.
Montgomery H, et al.
Acta Crystallographica, 22(6), 775-780 (1967)
Apoorvi Tyagi et al.
International journal of molecular sciences, 21(23) (2020-12-03)
Phenylketonuria (PKU) is an autosomal recessive metabolic disorder caused by the dysfunction of the enzyme phenylalanine hydroxylase (PAH). Alterations in the level of PAH leads to the toxic accumulation of phenylalanine in the blood and brain. Protein degradation mediated by...

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