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14160

Sigma-Aldrich

Sodium succinate dibasic

purum, anhydrous, ≥98.0% (NT)

Synonym(s):

Anhydrous butanedioic acid disodium salt, Succinic acid disodium salt

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About This Item

Linear Formula:
NaOOCCH2CH2COONa
CAS Number:
Molecular Weight:
162.05
Beilstein/REAXYS Number:
3917246
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

grade

purum

assay

≥98.0% (NT)

SMILES string

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

InChI

1S/C4H6O4.2Na/c5-3(6)1-2-4(7)8;;/h1-2H2,(H,5,6)(H,7,8);;/q;2*+1/p-2

InChI key

ZDQYSKICYIVCPN-UHFFFAOYSA-L

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Application

Sodium succinate dibasic can be used:
  • As a liquid phase in the study of basic properties of α-tricalcuim phosphate-based cement.
  • To prepare succinato-bridged copper(II) complexes exhibiting magnetic properties.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Effects of liquid phase on basic properties of α-tricalcium phosphate-based apatite cement
Oda M, et al.
Dental Materials Journal, 27, 672-677 (2008)
Succinato-bridged copper (II) supramolecular 3D framework: Synthesis, crystal structure and magnetic property
Ghoshal D, et al.
Inorgorganica Chimica Acta, 360, 1771-1775 (2007)
Polymeric networks of copper (II) using succinate and aromatic N-N donor ligands: synthesis, crystal structure, magnetic behaviour and the effect of weak interactions on their crystal packing
Ghoshal D, et al.
Dalton Transactions, 27, 1687-1695 (2004)
Makoto Oda et al.
Dental materials journal, 27(5), 672-677 (2008-11-01)
Effects of liquid phase on the basic properties of alpha-tricalcuim phosphate (alpha-TCP)-based cement, BIOPEX, were investigated by employing three liquid phases: distilled water, neutral sodium hydrogen phosphate solution, and succinic acid disodium salt solution containing sodium salt of chondroitin sulfate.
Davide Ret et al.
Carbohydrate polymers, 204, 124-130 (2018-10-28)
The purpose of the present study was the development of an accurate method to determine the degree of substitution (DS) of modified hyaluronic acid (HA) by proton nuclear magnetic resonance (1H NMR) spectroscopy. The influence of the effect of ionic

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