Tributylmethylphosphonium methylcarbonate, >97%, 50% in MeOH

Price range: $193.81 through $1,821.24

Product Code: IN-0030-SG

CAS NO: 120256-45-3

  • Chemical Formula: C15H33O3P
  • Synonyms: P1444 BTA, P1444 NTf2, P1444 TFSI, P1444 BTI

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SUM Formula: C15H33O3P

Molecular Weight: 292.22

Purity: >97%

  • SUM Formula: C15H33O3P
  • Molecular Weight: 292.22

Tributylmethylphosphonium methylcarbonate, CAS: 120256-45-3

Key Applications:

CO₂‑Derived Chemistry & Green Carbonylation

  • Functions as a reactive methylcarbonate donor in carbonylation, carboxymethylation, and carbonate‑forming reactions.
  • Supports CO₂‑utilization pathways, particularly in systems where methylcarbonate anions act as masked CO₂ equivalents.
  • Useful in developing sustainable synthesis routes for carbonates, carbamates, and alkyl carbonates.

Phase‑Transfer & Catalytic Media

  • Acts as an efficient phase‑transfer medium for nucleophilic substitution, esterification, and alkylation reactions.
  • Enhances reaction rates in biphasic and low‑polarity systems due to its high polarity and low volatility.
  • Serves as a tunable solvent/catalyst hybrid in organophosphonium‑mediated transformations.

 Polymer & Materials Processing

  • Employed as a processing aid and solvation medium for engineering polymers, including polycarbonates, polyurethanes, and cellulose derivatives.
  • Supports polymer functionalization via carbonate exchange or mild alkylation pathways.
  • Useful in membrane casting, ion‑conductive films, and surface modification workflows.

 Electrochemical & Energy Applications

  • Provides a stable ionic environment for electrolyte formulation, especially where carbonate anions improve SEI formation or interfacial stability.
  • Investigated in CO₂‑electroreduction, capacitive systems, and low‑volatility electrolytes requiring wide electrochemical windows.

 Extraction, Separation & Solvent Systems

  • Effective in liquid–liquid extraction of metal ions, organics, and CO₂‑reactive species.
  • Offers tunable polarity for selective separations, particularly where carbonate coordination or mild basicity is advantageous.
  • Useful as a green solvent alternative in replacing volatile organic carbonates.

 Specialty Synthesis & Fine Chemicals

  • Enables selective O‑methylation, carbonate exchange, and mild base‑promoted transformations.
  • Serves as a reagent/medium for preparing functionalized carbonates, protected alcohols, and intermediate building blocks.

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