Skip to Content
Merck
All Photos(1)

Key Documents

54345

Sigma-Aldrich

N-(2-Hydroxyethyl)iminodiacetic acid

≥98.0% (T)

Synonym(s):

Ethanol diglycine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HOCH2CH2N(CH2COOH)2
CAS Number:
Molecular Weight:
177.16
Beilstein:
1780628
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98.0% (T)

form

solid

mp

178 °C (lit.)

application(s)

peptide synthesis

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

Looking for similar products? Visit Product Comparison Guide

General description

N-(2-Hydroxyethyl)iminodiacetic acid (HEIDA) is a biodegradable and strong metal chelating agent, similar to nitrilotriacetic acid (NTA).

Application

N-(2-Hydroxyethyl)iminodiacetic acid (HEIDA) can be used in the following processes:
  • HEIDA can be used as a metal chelating agent for Fe(III) ion. The presence of HEIDA improves the Fenton′s destruction performance of PCE (perchloroethylene) existing as dense non-aqueous phase liquid (DNAPL) in soil slurry systems.
  • Oxorhenium(V) complexes with HEIDA are used for the carboxylation of ethane by CO, with potassium peroxodisulfate (K2S2O8)/trifluoroacetic acid (TFA), to afford propionic and acetic acid in good yield.
  • Vanadium complexes with HEIDA are used for the peroxidative hydroxylation of benzene and oxidation of mesitylene.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Single-Pot Ethane Carboxylation Catalyzed by New Oxorhenium (V) Complexes with N, O Ligands.
Kirillov AM, et al.
advanced synthesis and catalysis, 347(10), 1435-1446 (2005)
Single-Pot Ethane Carboxylation Catalyzed by New Oxorhenium (V) Complexes with N, O Ligands.
Kirillov AM, et al.
Advanced Synthesis & Catalysis, 347(10), 1435-1446 (2005)
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)
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, 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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service