Skip to Content
MilliporeSigma
All Photos(1)

Documents

127345

Sigma-Aldrich

4-(2-Thiazolylazo)resorcinol

97%

Synonym(s):

2-(2,4-Dihydroxyphenylazo)thiazole, TAR

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H7N3O2S
CAS Number:
Molecular Weight:
221.24
Beilstein/REAXYS Number:
204257
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:

assay

97%

mp

211 °C (dec.) (lit.)

SMILES string

Oc1ccc(\N=N\c2nccs2)c(O)c1

InChI

1S/C9H7N3O2S/c13-6-1-2-7(8(14)5-6)11-12-9-10-3-4-15-9/h1-5,13-14H/b12-11+

Inchi Key

SHNIKUXMZFPPCS-VAWYXSNFSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Useful for the spectrophotometric determination of trace metals.

Pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Y Kalyan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(5), 1235-1241 (2009-11-03)
A membrane optode was developed utilizing the 8-hydroxyquinaldine (HQ) facilitated preconcentration of UO(2)(2+) ions and subsequent colored complex formation of UO(2)(2+) with 4-(2-thiazolylazo)-resorcinol (TAR) in optode matrix. The composition of the membrane optode was optimized by scanning several extractants immobilized
L Evans et al.
Journal of chromatography. A, 911(1), 127-133 (2001-03-28)
A capillary electrophoresis method utilizing 4-(2-thiazolylazo)resorcinol (TAR) was developed to separate uranium, cobalt, cadmium, nickel, titanium and copper metal ions. TAR was chosen as the visible absorbing chelating ligand because of its ability to form stable complexes with a wide
Yue-Feng Zhou et al.
The Analyst, 136(2), 282-284 (2010-11-11)
A simple cyclopalladated complex of 4-(2-thiazolylazo)resorcinol showed a specific red-to-green colour change upon addition of organotin species in the acetonitrile-water medium.
Ali Benvidi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(5), 1380-1385 (2011-03-01)
The acidity constants of 4-(2-thiazolylazo)-resorcinol (TAR) were determined by the principal component-wavelet neural network (WNN). Biprotic acid mass balance equations, the distribution functions and the corresponding spectral profiles which were generated by a Gaussian model, have been considered to simulate
S R Bergmann et al.
Clinica chimica acta; international journal of clinical chemistry, 104(1), 53-63 (1980-05-21)
A simple and rapid colorimetric assay for non-esterified fatty acids (NEFA) was developed employing extraction of samples with 0.1 mol/l glycine (pH 2.7) and methoxyethanol : butyl ether, and formation of a copper-fatty acid soap detected with 4-(2-thiazolylazo)-resorcinol. The method

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service