215406
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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关于此项目
线性分子式:
(NH4)2Fe(SO4)2 · 6H2O
化学文摘社编号:
分子量:
392.14
NACRES:
NB.24
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
233-151-8
MDL number:
Assay:
98.5-101.5%
99%
99%
Grade:
ACS reagent
Form:
powder or crystals
产品名称
硫酸亚铁(II)铵 六水合物, ACS reagent, 99%
InChI key
MQLVWQSVRZVNIP-UHFFFAOYSA-L
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
SMILES string
N.N.O.O.O.O.O.O.[Fe++].OS([O-])(=O)=O.OS([O-])(=O)=O
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%
Quality Level
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Application
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。
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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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