Skip to Content
Merck
CN

H4271

N-(2-Hydroxyethyl)iminodiacetic acid

≥95% (titration)

Synonym(s):

Ethanol diglycine

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

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:
Assay:
≥95% (titration)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


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.


Still not finding the right product?


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



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library



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)



Global Trade Item Number

SKUGTIN
H4271-50G04061831836318