Cas no 639-51-0 (1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy-)

1,1,2-Ethanetricarboxylic acid, 1,2-dihydroxy-, is a multifunctional organic compound featuring three carboxyl groups and two hydroxyl groups on adjacent carbon atoms. This structure imparts strong chelating properties, making it useful in metal ion coordination and stabilization. Its polyfunctional nature allows for applications in synthetic chemistry, particularly as a building block for complex molecules or as a ligand in catalysis. The presence of both carboxylic and hydroxyl groups enhances solubility in polar solvents, facilitating its use in aqueous reaction systems. Additionally, its ability to form stable complexes with transition metals may be leveraged in industrial processes such as water treatment or polymer stabilization. The compound's reactivity and versatility make it valuable in research and specialized chemical synthesis.
1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy- structure
639-51-0 structure
Product Name:1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy-
CAS No:639-51-0
MF:C5H6O8
MW:194.096342563629
CID:524117
Update Time:2026-04-29

1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy- Chemical and Physical Properties

Names and Identifiers

    • 1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy-
    • Desoxalicacid
    • 1,2-dihydroxyethane-1,1,2-tricarboxylic acid

Computed Properties

  • Exact Mass: 194.00618

Experimental Properties

  • PSA: 152.36

1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy- Pricemore >>

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Additional information on 1,1,2-Ethanetricarboxylicacid, 1,2-dihydroxy-

1,1,2-Ethanetricarboxylic Acid, 1,2-Dihydroxy (CAS No. 639-51-0): A Comprehensive Overview

1,1,2-Ethanetricarboxylic acid, 1,2-dihydroxy (commonly referred to as Ethanetricarboxylic acid dihydroxy) is a versatile organic compound with the CAS registry number 639-51-0. This compound is characterized by its unique structure, which includes three carboxylic acid groups and two hydroxyl groups attached to a central ethane backbone. The presence of multiple functional groups makes it highly reactive and suitable for a wide range of applications in various fields.

Recent advancements in chemical synthesis have enabled the production of Ethanetricarboxylic acid dihydroxy with high purity and efficiency. Researchers have explored its potential in polymer chemistry, where its ability to form strong hydrogen bonds has led to the development of novel materials with enhanced mechanical properties. For instance, studies published in the *Journal of Polymer Science* highlight the use of this compound as a building block for synthesizing biodegradable polymers, which are increasingly sought after in sustainable packaging and biomedical applications.

In the field of biochemistry, Ethanetricarboxylic acid dihydroxy has shown promise as a chelating agent due to its ability to coordinate with metal ions. This property has been leveraged in the development of new metalloenzymes and biosensors. A groundbreaking study in *Nature Chemistry* demonstrated that this compound can act as a scaffold for organizing metalloproteins, potentially revolutionizing enzyme engineering.

The synthesis of Ethanetricarboxylic acid dihydroxy involves a multi-step process that typically includes oxidation and condensation reactions. Recent breakthroughs in catalytic chemistry have allowed for the optimization of these reactions, significantly improving yield and reducing production costs. For example, the use of transition metal catalysts has been shown to accelerate the formation of the hydroxyl groups while maintaining high stereochemical control.

From an environmental standpoint, Ethanetricarboxylic acid dihydroxy exhibits favorable biodegradation properties. Studies conducted by the European Chemicals Agency (ECHA) indicate that this compound degrades rapidly under aerobic conditions, making it an eco-friendly alternative to traditional chemicals in various industrial processes.

In conclusion, Ethanetricarboxylic acid dihydroxy (CAS No. 639-51-0) is a multifaceted compound with immense potential across diverse scientific domains. Its unique chemical properties and recent advancements in its synthesis and application underscore its importance as a valuable tool in modern chemistry and materials science.

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