Quality Level
assay
≥95% (titration)
mp
178 °C (lit.)
SMILES string
OCCN(CC(O)=O)CC(O)=O
InChI
1S/C6H11NO5/c8-2-1-7(3-5(9)10)4-6(11)12/h8H,1-4H2,(H,9,10)(H,11,12)
InChI key
JYXGIOKAKDAARW-UHFFFAOYSA-N
General description
N-(2-Hydroxyethyl)iminodiacetic acid is an organic building block shows different structural motifs. It has 3 bridging moieties that leads to the connects with rare earth metal centers so this can act as both bridging ligand as well as the chelating agent.
Application
N-(2-Hydroxyethyl)iminodiacetic acid can be used in the synthesis of polymeric solids.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A novel two dimensional samarium (III) coordination framework with N-(2-Hydroxyethyl) iminodiacetic acid and oxalate ligands: Synthesis, crystal structure and magnetic property
Zhao, et al.
Inorganic Chemistry Communications, 14, 1928-1931 (2011)
Lanthanide coordination polymers based on flexible ligands derived from iminodiacetic acid
Puentes, et al.
Polyhedron, 170, 683-689 (2019)
Namgoo Kang et al.
Chemosphere, 61(7), 909-922 (2005-11-01)
Fenton's destruction of benzene, toluene, ethylbenzene, and xylene (BTEX) was investigated in soil slurry batch reactors. The purpose of the investigation was to quantify the enhancement of oxidation rates and efficiency by varying process conditions such as iron catalyst (Fe(II)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| H4271-50G | 04061831836318 |
