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Merck
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Documentos Principais

F3629

Sigma-Aldrich

Ammonium iron(III) sulfate dodecahydrate

ReagentPlus®, ≥99%

Sinônimo(s):

Ammonium iron disulfate dodecahydrate, Ammonium ferric sulfate dodecahydrate

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About This Item

Fórmula linear:
NH4Fe(SO4)2 · 12H2O
Número CAS:
Peso molecular:
482.19
Número CE:
Número MDL:
Código UNSPSC:
12161600
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

linha de produto

ReagentPlus®

Ensaio

≥99%

adequação da reação

core: iron
reagent type: catalyst

pf

39-41 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

N.O.O.O.O.O.O.O.O.O.O.O.O.[Fe+3].OS([O-])(=O)=O.[O-]S([O-])(=O)=O

InChI

1S/Fe.H3N.2H2O4S.12H2O/c;;2*1-5(2,3)4;;;;;;;;;;;;/h;1H3;2*(H2,1,2,3,4);12*1H2/q+3;;;;;;;;;;;;;;;/p-3

chave InChI

LCPUDZUWZDSKMX-UHFFFAOYSA-K

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Aplicação

Ammonium iron(III) sulfate dodecahydrate can be used as:
  • A catalyst to synthesize 1,4-dihydropyridines via one-pot three-component condensation reaction of dimedone, aldehydes, and 3-aminocrotonate in ethanol.
  • An additive in the reduction of aromatic nitro compounds to the corresponding amino compounds in the presence of alumina-supported hydrazine hydrate as a catalyst.

Informações legais

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Corrosion

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Eye Dam. 1

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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The method is based upon the reaction between fluoride ions and the coloured complex of Fe(III) with methyl salicylate to form the stable, colourless hexaflouride complex of iron. The conditions of the method (pH, time and combination ratio) were studied
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M X Yang et al.
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The NADH-dependent microsomal electron transfer system consists of NADH-cytochrome b5 reductase and cytochrome b5, which donates reducing equivalents to fatty acyl desaturase, cytochrome P450, and other reactions. A study was carried out to investigate the interaction of NADH with several

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