Cas no 3105-55-3 (2-Butenedioic acid(2Z)-, sodium salt (1:1))

2-Butenedioic acid (2Z)-, sodium salt (1:1), also known as sodium maleate, is a water-soluble derivative of maleic acid with the molecular formula C?H?Na?O?. This compound is widely utilized in industrial and laboratory applications due to its role as an intermediate in organic synthesis, particularly in the production of polymers, resins, and surfactants. Its high solubility and reactivity make it suitable for use as a chelating agent and buffering agent in various chemical processes. The (2Z)-configuration ensures specific stereochemical properties, which can be advantageous in controlled reactions. Proper handling and storage are recommended to maintain stability.
2-Butenedioic acid(2Z)-, sodium salt (1:1) structure
3105-55-3 structure
Product Name:2-Butenedioic acid(2Z)-, sodium salt (1:1)
CAS No:3105-55-3
MF:C4H3NaO4
MW:138.053992509842
CID:308704
PubChem ID:87572135
Update Time:2025-10-12

2-Butenedioic acid(2Z)-, sodium salt (1:1) Chemical and Physical Properties

Names and Identifiers

    • 2-Butenedioic acid(2Z)-, sodium salt (1:1)
    • Monosodium Maleate Trihydrate
    • MALEIC ACID MONOSODIUM SALT
    • disodium 2-hydroxysuccinate
    • DI-SODIUM DL-MALATE
    • DISODIUM DL-MALATE HYDRATE
    • disodium malate
    • DI-SODIUM MALATE 0.5-WATER
    • Disodium maleate
    • disodium of maleic acid
    • dl-malic acid disodium
    • DL-MALIC ACID SODIUM
    • Dl-MalicAcid,SodiumSalt
    • Maleic Acid Monosodium Salt Trihydrate
    • maleic acid sodium salt
    • malic acid disodium salt
    • MALIC ACID, SODIUM
    • SODIUM DL-MALATE HYDRATE
    • sodium L-ma
    • Sodium malate
    • Sodium maleate
    • Toxilic acid
    • Sodium Bimaleate Trihydrate
    • Sodium Hydrogen Maleate Trihydrate
    • CCRIS 1121
    • CS-0185679
    • Sodium (Z)-3-carboxyacrylate
    • Sodium (2Z)-3-carboxyacrylate
    • Maleic acid sodium salt, BioXtra, >=99%
    • A876036
    • 2-Butenedioic acid (2Z)-, monosodium salt
    • UNII-EEL2016S8M
    • EEL2016S8M
    • Sodium hydrogen maleate
    • M0016
    • Maleic acid, monosodium salt
    • 30915-61-8
    • DTXSID40892502
    • MFCD00070246
    • EINECS 221-461-6
    • Sodium Bimaleate
    • HY-W127447
    • 3105-55-3
    • sodium;(Z)-4-hydroxy-4-oxobut-2-enoate
    • VRVKOZSIJXBAJG-ODZAUARKSA-M
    • 2-Butenedioic acid (2Z)-, sodium salt (1:1)
    • Maleic acid sodium salt, ~99%
    • Monosodium maleate
    • Q27277138
    • SODIUM ACID MALEATE
    • MDL: MFCD00070246
    • Inchi: 1S/C4H4O4.Na/c5-3(6)1-2-4(7)8;/h1-2H,(H,5,6)(H,7,8);/q;+1/p-1/b2-1-;
    • InChI Key: VRVKOZSIJXBAJG-ODZAUARKSA-M
    • SMILES: [Na+].[O-]C(/C=C\C(=O)O)=O

Computed Properties

  • Exact Mass: 137.99290285g/mol
  • Monoisotopic Mass: 137.99290285g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 2
  • Complexity: 119
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • XLogP3: -0.3
  • Topological Polar Surface Area: 74.6

Experimental Properties

  • Color/Form: White crystals.
  • Density: No data available
  • Melting Point: No data available
  • Flash Point: No data available
  • Solubility: H2O: 1?M at?20?°C, clear, colorless
  • Solubility: Soluble in water, insoluble in ethanol.

2-Butenedioic acid(2Z)-, sodium salt (1:1) Security Information

2-Butenedioic acid(2Z)-, sodium salt (1:1) Pricemore >>

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2-Butenedioic acid(2Z)-, sodium salt (1:1) Related Literature

Additional information on 2-Butenedioic acid(2Z)-, sodium salt (1:1)

Introduction to 2-Butenedioic acid (2Z)-, sodium salt (1:1) and Its Applications in Modern Chemical Biology

2-Butenedioic acid (2Z)-, sodium salt (1:1), with the CAS number 3105-55-3, is a significant compound in the field of chemical biology. This sodium salt of (2Z)-maleic acid has garnered considerable attention due to its versatile applications in pharmaceuticals, material science, and biochemical research. The compound's unique structural properties and reactivity make it a valuable tool for synthetic chemists and biologists alike.

The molecular structure of 2-Butenedioic acid (2Z)-, sodium salt (1:1) features a conjugated diene system with a carboxylate group at each end. This configuration imparts distinct electronic and steric properties, enabling its use in various chemical reactions and biological processes. The sodium salt form enhances solubility in aqueous solutions, making it particularly useful for applications in solution-phase synthesis and biomedical assays.

In recent years, research into 2-Butenedioic acid (2Z)-, sodium salt (1:1) has expanded significantly, particularly in the context of drug development and biomaterial design. Studies have highlighted its potential as a chelating agent for metal ions, which is crucial for developing targeted therapeutic agents. The compound's ability to form stable complexes with metals like iron and copper has opened new avenues for treating metal toxicity and enhancing metal-based drug formulations.

Moreover, the applications of (2Z)-maleic acid sodium salt extend to the field of polymer chemistry. Its incorporation into polymeric matrices can enhance the mechanical strength and thermal stability of materials. This property is particularly valuable in the production of high-performance plastics and coatings that require robust chemical resistance. Recent advancements in polymer science have demonstrated its efficacy in creating novel biodegradable polymers with improved environmental compatibility.

The biochemical significance of CAS no 3105-55-3 cannot be overstated. It serves as a key intermediate in the synthesis of various bioactive molecules. For instance, it has been utilized in the production of prostaglandin analogs, which are widely used in medicine for their anti-inflammatory properties. The compound's role in these synthetic pathways underscores its importance as a building block in medicinal chemistry.

Recent clinical trials have explored the potential of derivatives of 2-Butenedioic acid (2Z)-, sodium salt (1:1) in treating neurological disorders. The ability of this compound to modulate enzyme activity and ion channel function has led to promising results in preclinical studies. These findings suggest that further research could uncover novel therapeutic strategies for conditions such as epilepsy and neurodegenerative diseases.

The industrial relevance of (1:1) sodium salt of (2Z)-maleic acid is also evident in its use as a catalyst or co-catalyst in organic transformations. Its acidic nature makes it an effective proton donor in various reactions, including esterification and hydrolysis processes. This capability has been leveraged to optimize synthetic routes for producing fine chemicals and pharmaceutical intermediates.

In conclusion, CAS no 3105-55-3 represents a multifaceted compound with broad applications across multiple scientific disciplines. Its unique chemical properties make it indispensable in pharmaceutical research, material science, and biochemical investigations. As our understanding of its potential continues to grow, so too will its role in advancing scientific knowledge and technological innovation.

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