Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H10N2O5 |
Molecular Weight | 190.154 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)CN(CC(O)=O)CC(O)=O
InChI
InChIKey=QZTKDVCDBIDYMD-UHFFFAOYSA-N
InChI=1S/C6H10N2O5/c7-4(9)1-8(2-5(10)11)3-6(12)13/h1-3H2,(H2,7,9)(H,10,11)(H,12,13)
Molecular Formula | C6H10N2O5 |
Molecular Weight | 190.154 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
N-(2-Acetamido)iminodiacetic Acid is a biological buffer component with sodium hydroxide and sodium chloride (pH 5.67-7.57, useful pH range 6.4-7.4). N-(2-Acetamido)iminodiacetic Acid is used to prepare immobilized pH gradients.
ADA, or N-(2-Acetamido)iminodiacetic acid, can be used to study biological buffers and zwitterionic compounds. ADA has been used in a study to describe the application of scanning capacitively coupled contactless conductivity detection (SC(4)D) for the determination of pH dependant behaviour of two aminopolycarboxylates immobilised onto the surface of a monolithic capillary column. Blood cell stabilizing agent.
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20164337
Crystals were grown at 20°C by hanging-drop vapor diffusion method by mixing equal volumes of protein samples with reservoir solutions containing 1.2 m sodium/potassium tartrate and 100 mm N-(2-acetamido)iminodiacetic acid, pH 6.5.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:01:58 GMT 2023
by
admin
on
Sat Dec 16 04:01:58 GMT 2023
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Record UNII |
5C4R3O704E
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Record Status |
Validated (UNII)
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Record Version |
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117765
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5C4R3O704E
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DTXSID4067191
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ADA (buffer)
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DB02810
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m1405
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43960
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247-530-0
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26239-55-4
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