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Key Documents

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11-0130

Sigma-Aldrich

Ferroin indicator solution

Sinónimos:

1,10-Phenanthroline iron(II) sulfate complex, o-Phenanthroline ferrous sulfate complex

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About This Item

Fórmula lineal:
[Fe(C12H8N2)3]SO4
Número de CAS:
14634-91-4
Peso molecular:
692.52
MDL number:
MFCD00036428
UNSPSC Code:
41116100
PubChem Substance ID:
329749277

availability

available only in Japan

SMILES string

[Fe++].[O-]S([O-])(=O)=O.c1cnc2c(c1)ccc3cccnc23.c4cnc5c(c4)ccc6cccnc56.c7cnc8c(c7)ccc9cccnc89

InChI

1S/3C12H8N2.Fe.H2O4S/c3*1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;;1-5(2,3)4/h3*1-8H;;(H2,1,2,3,4)/q;;;+2;/p-2

InChI key

CIWXFRVOSDNDJZ-UHFFFAOYSA-L

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Suitability

for titration

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Jichang Wang et al.
The journal of physical chemistry. A, 109(7), 1374-1381 (2006-07-13)
The ferroin-catalyzed Belousov-Zhabotinsky (BZ) reaction was studied in a batch reactor under anaerobic conditions and was found to evolve through two separated regimes of complex oscillations. Significantly, the two bifurcation regimes exhibited qualitatively different dependence on compositions of the reaction
V H Tomasi et al.
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 78(5), 255-259 (2004-03-03)
We describe here a new method for specific staining of mast cells using ferroin. Different hamster tissues were fixed in 4% formalin and processed for paraffin embedding. Sections were stained with hematoxylin followed by ferroin acidified with 2.5 N sulfuric
Catalina Peralta et al.
The journal of physical chemistry. A, 110(44), 12145-12149 (2006-11-03)
The purpose of this research was to explore the unstirred, ferroin-catalyzed Belousov-Zhabotinsky (BZ) reaction as an experimental model for the response of excitable media to small perturbations (slightly larger than the threshold for excitations). Following Showalter et al. (Showalter, K.;
Luciano A Cardoso et al.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 151(3), 313-321 (2007-06-05)
Glutathione reductase (GR) carries out the enzymatic reduction of glutathione disulfide (GSSG) to its reduced form (GSH) at the expense of the reducing power of NADPH. Previous studies have shown that GR from several species is progressively inactivated in the
Laszló Hegedüs et al.
The journal of physical chemistry. A, 110(47), 12839-12844 (2006-11-28)
In the present mechanistic schemes of the ferroin-catalyzed oscillatory Belousov-Zhabotinsky (BZ) reaction the oxidation of the organic substrates (bromomalonic or malonic acid) by ferriin (the oxidized form of the catalyst) plays an important role. As the organic products of these
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