TTHA
Metal Chelate
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Product codeT031 TTHA
| Unit size | Price | Item Code |
|---|---|---|
| 5 g | ＄125.00 | T031-10 |
Chemical Structure
Introduction
Organic compounds that coordinate metal ions into circular structures (chelate circles) are called chelating reagents. Most chelating reagents include oxygen, nitrogen, or sulfur atoms in their molecules. Chelate structures with five or six member rings form the most stable chelate circle. In chelating reactions of typical chelating reagents, such as ethylenediamine, acetylacetone, and oxine, several molecules are coordinated with one metal ion. Ethylenediamine tetraacetic acid (EDTA), which has many coordinated atoms, forms a very stable chelate between one molecule of EDTA and metal ion. Chelating reagents are utilized for chelate titration, isolation, and separation of metal ions. They are also used to mask certain ions, solubilize metals in organic solvents, and for gas chromatography of metal ions. Metal indicators are chelating reagents that can be used to colorimetrically or fluorometrically determine metal ion concentration in solutions. Acetylacetone (AA) and its analogs are utilized for solvent extractions of metal ions from aqueous solutions. These metal complexes are used as catalysts of polymerization, dryness, and combustion. Chelating reagents, including EDTA, EDTA analogs, metal salts, and others, are available in bulk quantities from Dojindo. The following table indicates the stability constants of chelators with various metal ions and chelate reagents.
References
1) A. E. Martell, et al., “Chemistry of The Metal Chelate Compounds, EPrentice-Hall, Inc., New Jersey (1952);
2) G. Schwarzenbach, “Complexometric Titration, EH. Irving, Meteun & Co., Ltd., London; Interscinece Publishers, Inc., New York (1957);
3) F. J. Welcher, “The Analytical Uses of Ethylenediamine Tetraacetic Acid, ED. Van Nostrand Co., Inc., Prinston, Toronto, London, (1958);
4) H. Flaschka, “EDTA Titration E Pergamon Press, London, New York, Paris, Los Angeles, (1959);
5) S. Chaberek, A. E. Martell, “Organic Sequestering Agents, EJohn Wiley & Sons Inc., New York (1959);
6) R. L. Smith, “The Sequestration of Metals, EChapman & Hall Ltd., London (1959);
7) D. P. Graddon, “Introduction to Co-ordination Chemistry, E/font> Pergamon Press Ltd., (1961);
8) A. Ringbom, “Complexation in Analytical Chemistry, EJohn Wiley & Sons Inc., New York (1963);
9) T. S. West, “Complexometry with EDTA and Related Reagents, EBDH (1969);
10) R. Pribil, “Analytical Applications of EDTA and Related Compound, EPergamon Press Oxford, New York, Toronto, Syndey, Braunschweig (1972).
11) E. Bishop, “Indicators, EPergamon Press (1973).
Handling and storage condition
| Appearance： | White crystalline powder |
|---|---|
| Purity (Titration)： | ≧ 98.0 % |
| Solubility in NaOH solution： | To pass test (clear, colorless) |
| Sulfated ash： | ≦ 0.20 % |
| Heavy metals (as Pb)： | ≦ 0.001 % |
| Iron (Fe)： | ≦ 0.001 % |
| Ambient temperature |
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