Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H14N2O8.4Na |
| Molecular Weight | 394.1965 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CCCN(CC([O-])=O)CC([O-])=O)CC([O-])=O
InChI
InChIKey=YBAPEZRVAJFQCN-UHFFFAOYSA-J
InChI=1S/C11H18N2O8.4Na/c14-8(15)4-12(5-9(16)17)2-1-3-13(6-10(18)19)7-11(20)21;;;;/h1-7H2,(H,14,15)(H,16,17)(H,18,19)(H,20,21);;;;/q;4*+1/p-4
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Aminocarboxylate complexes of vanadium(III): Electronic structure investigation by high-frequency and -field electron paramagnetic resonance spectroscopy. | 2009-04 |
|
| Inner-sphere oxidation of ternary iminodiacetatochromium(III) complexes involving DL-valine and L-arginine as secondary ligands. Isokinetic relationship for the oxidation of ternary iminodiacetato-chromium(III) complexes by periodate. | 2009-02-04 |
|
| Coordination behaviour and two-dimensional-network formation in poly[[mu-aqua-diaqua(mu5-propane-1,3-diyldinitrilotetraacetato)dilithium(I)cobalt(II)] dihydrate]: the first example of an M(II)-1,3-pdta complex with a monovalent metal counter-ion. | 2008-06 |
|
| Determination of alternative and conventional chelating agents as copper(II) complexes by capillary zone electrophoresis--the first use of didecyldimethylammonium bromide as a flow reversal reagent. | 2007-02-12 |
|
| Improving sensitivity in simultaneous determination of copper carboxylates by nonaqueous capillary electrophoresis. | 2006-03-31 |
|
| Speciation of chromium(III) and cobalt(III) (amino)carboxylate complexes using capillary electrophoresis. | 2005-01-01 |
|
| Impact of aminopolycarboxylates on aquatic organisms and eutrophication: overview of available data. | 2004-12 |
|
| Occurrence of aminopolycarboxylates in the aquatic environment of Germany. | 2004-09 |
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DTXSID8027799
Created by
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7S77B8K8G4
Created by
admin on Mon Mar 31 22:23:58 GMT 2025 , Edited by admin on Mon Mar 31 22:23:58 GMT 2025
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167741
Created by
admin on Mon Mar 31 22:23:58 GMT 2025 , Edited by admin on Mon Mar 31 22:23:58 GMT 2025
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18719-03-4
Created by
admin on Mon Mar 31 22:23:58 GMT 2025 , Edited by admin on Mon Mar 31 22:23:58 GMT 2025
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PRIMARY |
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD