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Merck
CN

H4271

N-(2-Hydroxyethyl)iminodiacetic acid

≥95% (titration)

Synonym(s):

Ethanol diglycine

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About This Item

Linear Formula:
HOCH2CH2N(CH2COOH)2
CAS Number:
Molecular Weight:
177.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-263-9
Beilstein/REAXYS Number:
1780628
MDL number:
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Product Name

N-(2-Hydroxyethyl)iminodiacetic acid, ≥95% (titration)

InChI key

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)

SMILES string

OCCN(CC(O)=O)CC(O)=O

assay

≥95% (titration)

mp

178 °C (lit.)

Quality Level

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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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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)
Y Inoue et al.
Bioscience, biotechnology, and biochemistry, 60(5), 811-817 (1996-05-01)
A ras oncogene-amplified recombinant BHK-21 cell line (ras-rBHK-IgG) has been established, and was shown to hyperproduce the recombinant IgG chimeric human monoclonal antibody (hMAb) AE6F4, which recognizes lung cancer cells. We found that the ras-rBHK-IgG cell could be easily cultured
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)
Namgoo Kang et al.
Chemosphere, 63(10), 1685-1698 (2005-12-06)
The Fenton's system is applied to the destruction of perchloroethylene (PCE) present as a dense non-aqueous phase liquid (DNAPL) in soil slurry systems; the initial concentration of PCE was 45 times higher than its aqueous solubility. Studies were conducted in

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