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Sigma-Aldrich

Ethylenediaminetetraacetic acid calcium disodium salt hydrate

98%

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About This Item

Linear Formula:
Ca(O2CCH2)2NCH2CH2N(CH2CO2Na)2·xH2O
CAS Number:
304695-78-1
Molecular Weight:
374.27 (anhydrous basis)
MDL number:
MFCD00149453
UNSPSC Code:
12352116
PubChem Substance ID:
24860768
NACRES:
NA.22

assay

98%

form

powder

SMILES string

O.[Na]OC(=O)CN(CCN1CC(=O)O[Ca]OC(=O)C1)CC(=O)O[Na]

InChI

1S/C10H16N2O8.Ca.2Na.H2O/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20;;;;/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20);;;;1H2/q;+2;2*+1;/p-4

InChI key

JHECKPXUCKQCSH-UHFFFAOYSA-J

Application

Ethylenediaminetetraacetic acid calcium disodium salt hydrate is calcium and sodium salt of EDTA and it can be used:
  • To retain the quality of litchi fruit by the postharvest treatment process.
  • In the preparation of an aqueous solution for hydroxyapatite coating, which is used to coat the magnesium material/particle for biomedical applications.
  • To prepare a mobile phase for the separation of diol products from the aqueous solution of the reaction mixture by chromatography techniques.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

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’.

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Influence of modified atmosphere packaging and postharvest treatments on quality retention of litchi cv. Mauritius
Sivakumar D and Korsten L
Postharvest biology and technology, 41(2), 135-142 (2006)
Direct conversion of carbohydrates to diol by the combination of niobic acid and a hydrophobic ruthenium catalyst
Duan Y, et al.
Royal Society of Chemistry Advances, 7(42), 26487-26493 (2017)
Production and bio-corrosion resistance of porous magnesium with hydroxyapatite coating for biomedical applications
Kang M, et al.
Materials Letters, 108, 122-124 (2013)
Temmei Ito et al.
Biomedical materials (Bristol, England), 10(1), 015025-015025 (2015-03-03)
In order to obtain a hydroxyapatite (HAp)-poly(ethylene glycol) (PEG) composite, tetra amine-terminated PEG was crosslinked using disuccinimidyl tartrate to obtain a PEG hydrogel. Using two kinds of chelators with different stability constants for Ca ion (N-(2-hydroxyethyl) ethylenediamine-N,N',N'-triacetic acid (EDTA-OH, 8.14)

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