Disodium Succinate Hexahydrate - ≥98%(T) , CAS No.6106-21-4

CAS: 6106-21-4 Cat. No.: D154287 Molecular Weight: 270.14 Beilstein Registry Number: 3921040 EC Number: 612-073-1

GRADE & PURITY ≥98%(T)

Synonyms

Sodium succinate hexahydrate | disodium;butanedioate;hexahydrate | disodium succinate hexahydrate | Butanedioic acid disodium salt | Sodium succinate dibasic hexahydrate | U16QOD6C4E | Butanedioi cacid disodium salt

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

Sodium succinate dibasic hexahydrate is hexahydrate form of sodium succinate. It is generally used as a carbon source and electron donor in electrochemistry.

Specifications

Synonyms

Sodium succinate hexahydrate | disodium;butanedioate;hexahydrate | disodium succinate hexahydrate | Butanedioic acid disodium salt | Sodium succinate dibasic hexahydrate | U16QOD6C4E | Butanedioi cacid disodium salt

Specifications & Purity

≥98%(T)

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥98%(T)

Names and Identifiers

• Pubchem Sid: 488194253
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488194253
• Canonical Smiles: C(CC(=O)[O-])C(=O)[O-].O.O.O.O.O.O.[Na+].[Na+]
• IUPAC Name: disodium;butanedioate;hexahydrate
• InChIKey: ZBTUYCUNQBRXOR-UHFFFAOYSA-L
• INCHI: 1S/C4H6O4.2Na.6H2O/c5-3(6)1-2-4(7)8;;;;;;;;/h1-2H2,(H,5,6)(H,7,8);;;6*1H2/q;2*+1;;;;;;/p-2
• Isomeric SMILES: C(CC(=O)[O-])C(=O)[O-].O.O.O.O.O.O.[Na+].[Na+]
• WGK Germany: 1
• Molecular Weight: 270.14
• Beilstein: 3921040
• Reaxy-Rn: 3921044
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3921044&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Dicarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Dicarboxylic acids and derivatives
• Alternative Parents: Fatty acids and conjugates Carboxylic acid salts Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty acid - Dicarboxylic acid or derivatives - Carboxylic acid salt - Organic alkali metal salt - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.
• External Descriptors: hydrate

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: It is soluble in water at a concentration of 270 g/L at 20°C (68 °F)
• Sensitivity: Moisture sensitive.
• Molecular Weight: 270.140 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 1
• Exact Mass: 270.054 Da
• Monoisotopic Mass: 270.054 Da
• Topological Polar Surface Area: 86.300 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 81.600
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 9

XLogP3

References

1. Jun Li, Xiaosi Liang, Chenyang Zhao.  (2023)  Constructing poison-resistant Au-Pd single-atom alloy electrocatalyst on Pd nanocrystals for formic acid electrooxidation.  International Journal of Electrochemical Science,      [PMID:] [10.1016/j.ijoes.2023.100173]

2. Jing Gao, Li Chen, Zongcheng Yan.  (2015)  Phase Behavior of Aqueous Biphasic Systems Composed of Ionic Liquids and Organic Salts.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/je500419b]

3. Yuan Yu, Xiaoyun Zhang, Kai Lin.  (2024)  Analytical performance evaluation of hemoglobin A1c on an ARKRAY HA-8160 analyzer with newly-developed mobile phase buffer.  Practical Laboratory Medicine,      [PMID:38939102] [10.1016/j.plabm.2024.e00414]

4. Yiyao Zhang, Guangyun Zhang, Fen Yang, Zhikang Zou.  (2025)  Development of Mobile-Phase Buffers and Evaluation of Analytical Performance for HbA1c Assays.  BIOMEDICAL CHROMATOGRAPHY,  39  (10): (e70136).  [PMID:40884333] [10.1002/bmc.70136]