Skip to Content
Merck
All Photos(3)

Key Documents

234877

Sigma-Aldrich

Sodium iminodiacetate dibasic hydrate

98%

Synonym(s):

Iminodiacetic acid disodium salt hydrate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C4H5NO4Na2 · xH2O
CAS Number:
Molecular Weight:
177.07 (anhydrous basis)
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

SMILES string

O.[Na+].[Na+].[O-]C(=O)CNCC([O-])=O

InChI

1S/C4H7NO4.2Na.H2O/c6-3(7)1-5-2-4(8)9;;;/h5H,1-2H2,(H,6,7)(H,8,9);;;1H2/q;2*+1;/p-2

InChI key

YSBGCHXLMBAKPV-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Application

Sodium iminodiacetate dibasic hydrate (Iminodiacetic acid disodium salt monohydrate) has been used in the preparation of:
  • different iminodiacetic acid-agarose supports, useful for selective adsorption of large proteins
  • N-(o-hydroxybenzyl) iminodiacetic acid (multidentante ligand)

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary 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

Benevides C C Pessela et al.
Journal of chromatography. A, 1055(1-2), 93-98 (2004-11-25)
A strategy to selectively adsorb large proteins on immobilized metal ion affinity chromatography supports is presented. It is based on the fact that large proteins have a large surface that permits the long distance interaction with groups placed quite far
New multidentate ligands. XVII. Chelating tendencies of N-(o-hydroxybenzyl) iminodiacetic acid (H3L).
Harris WR, et al.
Inorganic Chemistry, 14(5), 974-978 (1975)

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