Tetrahydroxy-1,4-benzoquinone Disodium Salt TCI T0122

Chemical Identity

CAS No.: 1887-02-1
PubChem: CID 74675·SID 87576129
Formula: C6H2Na2O6
Molecular weight: 216.06 g/mol
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: disodium;4,6-dihydroxy-2,5-dioxocyclohexa-3,6-diene-1,3-diolate
SMILES: C1(=C(C(=O)C(=C(C1=O)O)[O-])[O-])O.[Na+].[Na+]
InChIKey: SOSMJTGSYNGZAV-UHFFFAOYSA-L

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TCI T0122 Tetrahydroxy-1,4-benzoquinone Disodium Salt is the sodium salt of tetrahydroxy-1,4-benzoquinone. Its molecule has a quinone ring with four functional oxygen groups around it. In the laboratory it is classed as a non-heterocyclic building block. It is redox-active and can act as a bridging ligand for metal ions. This makes it useful for synthesis in coordination chemistry, for research on functional materials, and for electrochemical studies of organic compounds that can store and release electrons.

Researchers choose this compound mainly because its quinone-enolate system can undergo stepwise, reversible redox reactions. That behaviour matters in research on organic electrode materials. The oxygen groups are arranged symmetrically, so the molecule can bridge two metal centres and build coordination polymers or higher-dimensional metal-organic frameworks. As a sodium salt, it is easier to handle and dissolves more readily in aqueous media than the acid form. This gives researchers more practical control when preparing solutions and running reactions in the lab.

The compound is usually a dark-coloured solid that is sensitive to air oxidation and moisture, so it needs careful handling during routine work. Interest in energy storage research keeps growing in Indonesia, including work on battery development. University research groups, materials science laboratories and electrochemistry teams can use this building block to explore redox-active organic systems and to synthesise new coordination compounds. It also suits research on functional materials and teaching projects in synthetic and coordination chemistry.

Related TCI products

Coordination chemistry synthesis: the symmetrically arranged oxygen groups can bridge two metal centres, so the compound is a useful ligand for building new metal complexes and coordination polymers.
Metal-organic framework research: because it bridges metal ions, the molecule can help form higher-dimensional frameworks, which suits studies on the design of porous and functional materials.
Organic electrode material studies: its quinone-enolate system undergoes stepwise, reversible redox reactions, so it is relevant to research on organic materials for energy storage electrodes.
Electrochemistry of organic compounds: the redox-active quinone core can store and release electrons, which makes it a good model compound for electrochemical studies of electron-transfer behaviour.
Aqueous-phase reactions and solution preparation: as a sodium salt it dissolves more readily in aqueous media than the acid form, so it is practical for reactions and analyses that need water-based solutions.

Brand	TCI (product code T0122)
CAS number	1887-02-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	available in the pack sizes TCI supplies for this product code
Physical form	usually a dark-coloured solid
Storage	sensitive to air oxidation and moisture; keep tightly sealed and protected

This compound is sensitive to air oxidation and moisture. Keep it in a tightly sealed container, ideally the original supplier packaging, in a cool, dry place away from direct light and incompatible substances. After opening, reduce exposure to air by closing the container right after use. Where possible, store it under an inert atmosphere or in a desiccator. Handle the material in a well-ventilated area or a fume hood, and wear suitable personal protective equipment such as gloves, safety glasses and a lab coat. Avoid creating dust, and do not let the material touch skin or eyes. Always read the supplier's Safety Data Sheet before use, and follow local regulations for disposing of chemical waste.

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