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Merck

323209

Sigma-Aldrich

4-(2-Pyridylazo)resorcinol

96%

Sinónimos:

PAR

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About This Item

Fórmula empírica (notación de Hill):
C11H9N3O2
Número de CAS:
Peso molecular:
215.21
Beilstein/REAXYS Number:
184665
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

Quality Level

assay

96%

form

powder

composition

Carbon: 58.6-64.2%

Nitrogen: 18.6-20.4%

technique(s)

titration: suitable

color

brown-red

mp

192-202 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

Oc1ccc(\N=N\c2ccccn2)c(O)c1

InChI

1S/C11H9N3O2/c15-8-4-5-9(10(16)7-8)13-14-11-3-1-2-6-12-11/h1-7,15-16H/b14-13+

InChI key

RJNYNDHYSJRRDW-BUHFOSPRSA-N

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General description

4-(2-Pyridylazo)resorcinol (PAR) is a monosodium salt(1), dibasic acid that forms the protonated complexes with most metal ions.

Application

4-(2-Pyridylazo)resorcinol (PAR) serves as a metallochromic indicator and is suitable as a chromogenic agent for the quantitative determination of over 50 elements.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Douglas A Mitchell et al.
Biochemistry, 44(12), 4636-4647 (2005-03-23)
The inducible isoform of nitric oxide synthase (iNOS) and three zinc tetrathiolate mutants (C104A, C109A, and C104A/C109A) were expressed in Escherichia coli and purified. The mutants were found by ICP-AES and the zinc-specific PAR colorimetric assay to be zinc free
Tahereh Rohani et al.
Talanta, 80(5), 1827-1831 (2010-02-16)
A 4-(2-pyridylazo)-resorcinol (PAR)-modified carbon ceramic electrode (CCE) prepared by the sol-gel technique has been reported for the first time in this paper. By immersing the CCE in aqueous solution of PAR (0.001molL(-1)), after a short period of time, a thin
Leon Barron et al.
Journal of chromatography. A, 1213(1), 31-36 (2008-09-10)
The selectivity, retention and separation of transition metals on a short (2 mm x 50 mm) column packed with a poly-iminodiacetic acid functionalised polymer 10 microm resin (Dionex ProPac IMAC-10) are presented. This stationary phase, typically used for the separation
William K Boyle et al.
PLoS pathogens, 17(2), e1009072-e1009072 (2021-02-19)
Throughout its enzootic cycle, the Lyme disease spirochete Borreliella (Borrelia) burgdorferi, senses and responds to changes in its environment using a small repertoire of transcription factors that coordinate the expression of genes required for infection of Ixodes ticks and various
Gilles Montavon et al.
Dalton transactions (Cambridge, England : 2003), 39(5), 1366-1374 (2010-01-28)
Literature reports of the efficacy of para-sulfonatocalix[6]- and calix[8]-arenes as U(vi) complexants indicated that they might be useful for in vivo chelation of the novel therapeutic alpha-emitter (230)U. We have studied the complexation of U(vi) with para-sulfonatocalix[6]arene and para-sulfonatocalix[8]arene by

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