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Merck
CN

215406

Sigma-Aldrich

硫酸亚铁(II)铵 六水合物

ACS reagent, 99%

别名:

亚铁铵矾, 硫酸亚铁铵 六水合物, 莫尔盐

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About This Item

线性分子式:
(NH4)2Fe(SO4)2 · 6H2O
CAS号:
分子量:
392.14
EC 号:
MDL编号:
UNSPSC代码:
12352302
PubChem化学物质编号:
NACRES:
NB.24
方案:
98.5-101.5%
99%
等级:
ACS reagent
表单:
powder or crystals

等级

ACS reagent

质量水平

方案

98.5-101.5%
99%

表单

powder or crystals

反应适用性

reagent type: catalyst
core: iron

杂质

≤0.01% insolubles
≤0.05% Not NH4OH pptd.

pH值(酸碱度)

3-5 (20 °C, 50 g/L)

mp

100 °C (dec.) (lit.)

痕量阴离子

phosphate (PO43-): ≤0.003%

痕量阳离子

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字符串

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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应用

六水硫酸铁(II)铵可作为绿色催化剂用于:
  • 通过 Newman-Kwart 重排合成功能化噻吩。
  • 将芳香族、脂肪族和共轭醛氧化成相应的羧酸。
  • 通过缩合反应合成双香豆素。

储存分类代码

13 - Non Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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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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