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Merck
CN

P4272

3-(2-Pyridyl)-5,6-di(2-furyl)-1,2,4-triazine-5′,5′′-disulfonic acid disodium salt

Powder or crystals

Synonym(s):

5,5′-[3-(2-Pyridyl)-1,2,4-triazine-5,6-diyl]difuran-2-sulfonic acid disodium salt

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About This Item

Empirical Formula (Hill Notation):
C16H8N4Na2O8S2
CAS Number:
79551-14-7
Molecular Weight:
494.37
NACRES:
NA.47
PubChem Substance ID:
24898520
UNSPSC Code:
12171500
MDL number:
MFCD00040642
Beilstein/REAXYS Number:
5710932

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Product Name

3-(2-Pyridyl)-5,6-di(2-furyl)-1,2,4-triazine-5′,5′′-disulfonic acid disodium salt, Suitable for determination of Fe

InChI

1S/C16H10N4O8S2.2Na/c21-29(22,23)12-6-4-10(27-12)14-15(11-5-7-13(28-11)30(24,25)26)19-20-16(18-14)9-3-1-2-8-17-9;;/h1-8H,(H,21,22,23)(H,24,25,26);;/q;2*+1/p-2

SMILES string

[Na+].[Na+].[O-]S(=O)(=O)c1ccc(o1)-c2nnc(nc2-c3ccc(o3)S([O-])(=O)=O)-c4ccccn4

InChI key

IVLSEFOVPQFJBB-UHFFFAOYSA-L

form

powder or crystals

composition

Water: ≤ 13.0%

Carbon (Theory), anhydrous: 38.87%

Nitrogen (Theory), anhydrous: 11.33%

technique(s)

titration: suitable

color

white to dark yellow

solubility

water: 50 mg/mL, clear to slightly hazy

cation traces

C: 38.87% ((Theory), anhydrous)
N: 11.33% ((Theory), anhydrous)

suitability

suitable for determination of iron

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

200

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Application

3-(2-Pyridyl)-5,6-di(2-furyl)-1,2,4-triazine-5′,5′′-disulfonic acid disodium salt has been used as a component in a sensitive colorimetric assay (ferene-s assay) for the detection of iron. It has also been used as a ligand to study the complexation towards copper(II).

General description

3-(2-Pyridyl)-5,6-di(2-furyl)-1,2,4-triazine-5′,5′′-disulfonic acid disodium salt, also known as Ferene, is a chelating agent commonly used to measure the concentration of iron ions in aqueous solutions. The reagent is sensitive to ferrous iron ions (Fe2+) and forms a purple-colored complex with these ions in the presence of a reducing agent. The intensity of the purple color formed is proportional to the concentration of iron ions present in a solution and is quantified spectrophotometrically.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9759
BCCN9275
BCCN3166
BCCM6745
BCCL3263

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Synthesis, Characterization, and Antimicrobial Activity of Novel Sulfonated Copper?Triazine Complexes.
Katugampala S, et al.
Bioinorganic Chemistry and Applications, 2530851-2530851 (2018)
A facile colorimetric method for the quantification of labile iron pool and total iron in cells and tissue specimens.
Abbasi U, et al.
Scientific Reports, 6008, 11(1)-11(1) (2021)
J D Artiss et al.
American journal of clinical pathology, 108(3), 269-274 (1997-09-18)
We describe a modification of a previously described serum iron procedure applied to the Bayer DAX48 (Bayer Diagnostics, Tarrytown, NY) automated chemistry analyzer. The iron-ligand used in this assay, 2-(5-nitro-2-pyridylazo)-5-(N-propyl-N-sulfopropylamine) phenol (nitro-PAPS), has a molar absorptivity of 94,000 L mol(-1)
Novel chromogen for serum iron determinations.
T Higgins
Clinical chemistry, 27(9), 1619-1620 (1981-09-01)
L M Leong et al.
Analytical biochemistry, 207(2), 317-320 (1992-12-01)
Nonheme iron proteins can be visualized as blue bands in native polyacrylamide gels using a staining method that is both simple and rapid. The reaction of potassium ferricyanide with protein-bound iron atoms to form royal blue complexes occurs almost instantaneously
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