Cas no 274257-37-3 (Tributylmethylammonium methyl carbonate)

Tributylmethylammonium methyl carbonate is a quaternary ammonium salt with applications as a phase-transfer catalyst and electrolyte component in electrochemical systems. Its key advantages include high thermal stability, low viscosity, and good solubility in organic solvents, making it suitable for use in reactions requiring efficient mass transfer. The compound’s methyl carbonate anion contributes to its reactivity in carboxylation and esterification processes. Additionally, its ionic nature enhances conductivity in battery applications. The product is often utilized in synthetic chemistry and energy storage research due to its balanced properties, offering a reliable option for catalytic and electrochemical applications.
Tributylmethylammonium methyl carbonate structure
274257-37-3 structure
Product Name:Tributylmethylammonium methyl carbonate
CAS No:274257-37-3
MF:C13H30N+.C2H3O3-
MW:275.42742
CID:248083
PubChem ID:24885092
Update Time:2025-06-08

Tributylmethylammonium methyl carbonate Chemical and Physical Properties

Names and Identifiers

    • Tributylmethylammonium methyl carbonate
    • methyl carbonate,tributyl(methyl)azanium
    • methyl carbonate;tributyl(methyl)azanium
    • 274257-37-3
    • Methyltributylammonium methyl carbonate
    • SCHEMBL2230485
    • N,N-Dibutyl-N-methylbutan-1-aminium methyl carbonate
    • DTXSID20584832
    • TRIBUTYL(METHYL)AZANIUM METHYL CARBONATE
    • HS-3013
    • MFCD09265058
    • MDL: MFCD09265058
    • Inchi: InChI=1S/C13H30N.C2H4O3/c1-5-8-11-14(4,12-9-6-2)13-10-7-3;1-5-2(3)4/h5-13H2,1-4H3;1H3,(H,3,4)/q+1;/p-1
    • InChI Key: ZKWSMHMGQLTZGI-UHFFFAOYSA-M
    • SMILES: C(=O)([O-])OC.[N+](C)(CCCC)(CCCC)CCCC

Computed Properties

  • Exact Mass: 275.24619
  • Monoisotopic Mass: 275.24604391g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 9
  • Complexity: 133
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 49.4?2

Experimental Properties

  • Flash Point: Fahrenheit: 134.6 ° f < br / > Celsius: 57 ° C < br / >
  • Refractive Index: n20/D 1.408
  • PSA: 49.36
  • Color/Form: ~50% in methanol: water (2:3)

Tributylmethylammonium methyl carbonate Security Information

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Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHENG KE LU SI SHENG WU JI SHU
sc-237265-100 g
Tributylmethylammonium methyl carbonate solution,
274257-37-3
100g
¥3,761.00 2023-07-10
SHENG KE LU SI SHENG WU JI SHU
sc-237265-100g
Tributylmethylammonium methyl carbonate solution,
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Tributylmethylammonium methyl carbonate Related Literature

Additional information on Tributylmethylammonium methyl carbonate

Research Brief on Tributylmethylammonium Methyl Carbonate (CAS: 274257-37-3) in Chemical and Biomedical Applications

Tributylmethylammonium methyl carbonate (CAS: 274257-37-3) is an ionic liquid compound that has garnered significant attention in recent years due to its unique physicochemical properties and potential applications in chemical synthesis, catalysis, and biomedical fields. This research brief synthesizes the latest findings on this compound, focusing on its synthesis, characterization, and emerging applications.

Recent studies have highlighted the role of tributylmethylammonium methyl carbonate as a green solvent and catalyst in organic synthesis. Its low volatility, high thermal stability, and tunable solvation properties make it an attractive alternative to traditional volatile organic compounds (VOCs). A 2023 study published in Green Chemistry demonstrated its effectiveness as a reaction medium for Heck coupling reactions, achieving yields of up to 92% while significantly reducing environmental impact compared to conventional solvents.

In the biomedical field, researchers have explored the potential of 274257-37-3 as a drug delivery enhancer. Its amphiphilic nature allows it to improve the solubility and bioavailability of poorly water-soluble pharmaceuticals. A recent Journal of Controlled Release publication reported that formulations containing tributylmethylammonium methyl carbonate increased the oral absorption of a model anticancer drug by 3.5-fold compared to standard formulations, without observable toxicity in preclinical models.

Advanced characterization techniques, including NMR spectroscopy and mass spectrometry, have provided new insights into the molecular interactions of this compound. X-ray crystallography studies have revealed its unique three-dimensional structure, which contributes to its exceptional stability and solvent properties. These structural insights are guiding the design of next-generation ionic liquids with tailored properties for specific applications.

From a safety perspective, recent toxicological assessments indicate that tributylmethylammonium methyl carbonate exhibits low acute toxicity (LD50 > 2000 mg/kg in rodent studies) and minimal environmental persistence. However, researchers emphasize the need for further long-term ecotoxicological studies, particularly regarding its potential accumulation in aquatic systems.

Looking forward, several research groups are investigating the use of 274257-37-3 in energy storage applications, particularly as an electrolyte additive in lithium-ion batteries. Preliminary results suggest it may improve battery performance at extreme temperatures while enhancing safety characteristics. The compound's potential in CO2 capture technologies is also under active investigation, with promising early-stage results showing high selectivity for carbon dioxide absorption.

This brief highlights the growing importance of tributylmethylammonium methyl carbonate across multiple scientific disciplines. As research continues, we anticipate seeing expanded applications of this versatile compound, particularly in areas requiring environmentally benign alternatives to conventional chemicals. Future studies should focus on scaling up production methods and further elucidating structure-activity relationships to fully exploit its potential.

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