| Names | |
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IUPAC name
2-[(2-amino-2-oxoethyl)-(carboxymethyl)amino]acetic acid
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| Other names
ADA, N-(2-acetamido)iminodiacetic acid, N-(carbamoylmethyl)iminodiacetic acid
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| Identifiers | |
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3D model (JSmol)
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| EC Number | 247-530-0 |
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PubChem CID
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| UNII | |
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| Properties | |
| C6H10N2O5 | |
| Molar mass | 190.155 g/mol |
| Acidity (pKa) | 6.6 |
| Hazards | |
| Main hazards | Irritant |
| GHS signal word | Warning |
| H302, H315, H319, H335 | |
| P261, P264, P270, P271, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313 | |
| Flash point | Non-flammable |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
ADA is a zwitterionic organic chemical buffering agent; one of Good's buffers. It has a useful pH range of 6.0-7.2 in the physiological range, making it useful for cell culture work. It has a pKa of 6.6 with ΔpKa/°C of -0.011 and is most often prepared in 1 M NaOH where it has a solubility of 160 mg/mL.
ADA has been used in protein-free media for chicken embryo fibroblasts, as a chelating agent for H+, Ca2+, and Mg2+, and for isoelectric focusing in immobilized pH gradients. Its effects on dog kidney Na+/K+-ATPase and rat brain GABA receptors have also been studied. ADA does, however, alter coloring in bicinchoninic acid assays.