Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H11NO5 |
| Molecular Weight | 177.1552 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCN(CC(O)=O)CC(O)=O
InChI
InChIKey=JYXGIOKAKDAARW-UHFFFAOYSA-N
InChI=1S/C6H11NO5/c8-2-1-7(3-5(9)10)4-6(11)12/h8H,1-4H2,(H,9,10)(H,11,12)
| Molecular Formula | C6H11NO5 |
| Molecular Weight | 177.1552 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Mobility of radionuclides in soil/groundwater system: comparing the influence of EDTA and four of its degradation products. | 2010-10 |
|
| 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 |
|
| Enhanced Fenton's destruction of non-aqueous phase perchloroethylene in soil systems. | 2006-06 |
|
| Enhanced chemical oxidation of aromatic hydrocarbons in soil systems. | 2005-11 |
|
| Enhanced uptake of As, Zn, and Cu by Vetiveria zizanioides and Zea mays using chelating agents. | 2005-09 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:50:46 GMT 2025
by
admin
on
Mon Mar 31 22:50:46 GMT 2025
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| Record UNII |
BPQ4R5AF5K
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| Record Status |
Validated (UNII)
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| Record Version |
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EPA PESTICIDE CODE |
39104
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DTXSID4042177
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93-62-9
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