Ethylenediaminediacetic acid
Appearance
Names | |
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Preferred IUPAC name
2,2′-[Ethane-1,2-diylbis(azanediyl)]diacetic acid | |
Other names
N,N′-Ethylenediglycine
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.024.641 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C6H12N2O4 | |
Molar mass | 176.172 g·mol−1 |
Appearance | white solid |
Melting point | 228 °C (442 °F; 501 K) |
Hazards | |
GHS labelling:[1] | |
Danger | |
H302, H315, H318, H319, H335, H411 | |
P261, P264, P264+P265, P270, P271, P273, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Ethylenediaminediacetic acid (EDDA) is the organic compound with the formula C2H4(NHCH2CO2H)2. It is a derivative of two molecules of glycine, wherein the amines are linked. It is a white solid. It is one of several aminopolycarboxylic acids.
The conjugate base is a tetradentate ligand.[1] A representative complex is Na[Co(EDDA)(CO3)].[2]
Related compounds
[edit]References
[edit]- ^ Sabo, Tibor J.; Grguric-Sipka, Sanja R.; Trifunovic, Srecko R. (2002). "Transition Metal Complexes with EDDA-Type Ligands-a Review". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry. 32: 1661–1717. doi:10.1081/SIM-120015086. S2CID 94409799.
- ^ Leon J. Halloran; Arlene L. Gillie; J. Ivan Legg (1978). "Ethylenediamine- N,N ′-Diacetic Acid Complexes of Cobalt(III)". Inorganic Syntheses. Vol. 18. pp. 103–111. doi:10.1002/9780470132494.ch17. ISBN 978-0-470-13249-4.