Iminodiacetic acid
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Iminodiacetic acid | |
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File:Iminodiacetic acid.png | |
2-(carboxymethylamino)acetic acid | |
Other names Diglycolamidic acid | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 142-73-4 |
PubChem | 8897 |
ChemSpider | 8557 |
EC-number | 205-555-4 |
SMILES | Script error: No such module "collapsible list". |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C4H7NO4 |
Molar mass | 133.1 g mol−1 |
Density | 1.436 g/cm3 |
Melting point |
247.5 ºC |
style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
EU Index | not listed |
Flash point | 178 °C |
(what is this?) (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Infobox references |
Iminodiacetic acid, HN(CH2CO2H)2, often abbreviated to IDA, is an dicarboxylic acid amine. The iminodiacetate anion can act as a tridentate ligand to form a metal complex with two, fused, five membered chelate rings.[1] The proton on the nitrogen atom can be replaced by a carbon atom of a polymer to create an ion-exchange resin, such as chelex 100.
IDA forms stronger complexes than the bidentate ligand glycine and weaker complexes than the tetradentate ligand nitrilotriacetic acid.
See also
References
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- ↑ Schwarzenbach, G (1952). "Der Chelateffekt". Helv. Chim. Acta. 35: 2344–2359. doi:10.1002/hlca.19520350721.