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| | ARSENAZO I Basic information |
| Product Name: | ARSENAZO I | | Synonyms: | ARSENAZO 1;ARSENAZO I;2-(O-ARSONOPHENYLAZO)-1,8-DIHYDROXYNAPHTHALENEDISULFONIC ACID, SODIUM SALT;2-(1,8-DIHYDROXY-3,6-DISULFO-2-NAPHTHYLAZO)BENZENEARSONIC ACID TRISODIUM SALT;2-(1,8-DIHYDROXY-3,6-DISULFO-2-NAPHTHYLAZO)PHENYLARSONIC ACID DISODIUM SALT;2-(2-ARSONOPHENYLAZO)CHROMOTROPIC ACID DISODIUM SALT;O-(1,8-DIHYDROXY-3,6-DISULFO-2-NAPHTHYLAZO)BENZENEARSONIC ACID SODIUM SALT;O-(1,8-DIHYDROXY-3,6-DISULFO-2-NAPHTHYLAZO)BENZENEARSONIC ACID TRIHYDRATE | | CAS: | 520-10-5 | | MF: | C16H13AsN2O11S2 | | MW: | 548.33 | | EINECS: | 208-285-5 | | Product Categories: | | | Mol File: | 520-10-5.mol |  |
| | ARSENAZO I Chemical Properties |
| Melting point | ≥300 °C(lit.) | | solubility | methanol: 1 mg/mL, clear, red | | pka | -0.71±0.40(Predicted) | | form | Dark red powder. |
| | ARSENAZO I Usage And Synthesis |
| Chemical Properties | bordeaux powder | | Uses | The reagent reacts with many metal ions, such as uranium(IV), thorium(IV),
zirconium(IV), scandium(III), lanthanum(III), cerium(III), aluminium(III), beryllium(
III), titanium(III), niobium(lll), tantalum(III), vanadium(IV), tin(IV), bismuth(
III), gallium(III), copper(III), palladium(II), magnesium(II) and calcium(II)
to give coloured complexes. It has been used for the photometric determination
of the majority of the above-listed metal ions. Though the reagent reacts
with such a variety of metal ions, the complex formation reaction may be made
selective for individual metal ions by appropriate choice of the reaction conditions,
primarily of the pH of the solution. For instance, thorium can be determined
with Arsenazo I in the presence of almost all rare earth metals, and
similarly zirconium and thorium in the presence of uranium, etc.
The stabilities of the metal complexes of Arsenazo I are lower than those of the
corresponding complexes of EDTA. It can also therefore be used advantageously
as indicator in complexometric determination of some metals (e.g. plutonium,
thorium).
The analytical sensitivity of the formation of Arsenazo I complexes is comparatively
high (0.05-0.1 γ/ml). However, the importance of the reagent is decreasing
in analytical practice, in parallel with an increase in significance of the
related reagent, Arsenazo III, which gives more stable complexes with higher
absorbances, and which is therefore of greater analytical sensitivity. |
| | ARSENAZO I Preparation Products And Raw materials |
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