1-Methyl-3-nonylimidazolium hexafluorophosphate, >99%

Price range: $384.12 through $5,555.88

Product Code: IL-0308-HP

CAS NO: 343952-29-4

  • Chemical Formula: C13H25F6N2P
  • Synonyms: NonylMIM PF 6, C 1 C 9 Im PF 6, Im 19 PF 6
  • Anion decomposes slowly in the presence of water.
  • Aromatic
  • Hydrophobic
Clear

SUM Formula: C13H25F6N2P

Molecular Weight: 354.32

Melting Point: <RT

Purity: >99%

  • SUM Formula: C13H25F6N2P
  • Molecular Weight: 354.32
  • Melting Point:

1-Methyl-3-nonylimidazolium hexafluorophosphate, CAS: 343952-29-4

Key Applications:

Solvent and Electrolyte Applications

  • Non‑aqueous electrolyte component in electrochemical systems requiring high electrochemical stability and controlled viscosity.
  • Solvent or co‑solvent for transition‑metal catalysis, improving solubility of organometallic complexes and enabling enhanced reaction rates.
  • Medium for electrodeposition of metals and alloys, where hydrophobic ionic environments support uniform film formation.

Materials Science, Nanostructures, and Magnetic Systems

  • Template and dispersant for synthesizing metal nanoparticles, metal oxides, and hybrid nanomaterials, with the C9 alkyl chain enabling tunable micellar or lamellar structures.
  • Processing aid for polymers and ion‑conductive membranes, where the ionic liquid modulates morphology, conductivity, and mechanical properties.
  • Surface modification agent for creating hydrophobic, ion‑rich interfaces on silica, carbon materials, and metal oxides.
  • Magnetic‑responsive medium in systems incorporating paramagnetic or superparamagnetic species, where the ionic liquid’s low volatility and structural organization support stable dispersions and controlled magnetic manipulation.
  • Carrier phase for magnetic nanofluids and magnetically switchable materials, enabling field‑responsive viscosity, alignment, or separation behavior.

Separation Science and Extraction

  • Hydrophobic extraction phase for liquid–liquid separations involving aromatic hydrocarbons, sulfur‑containing compounds, or metal ions.
  • Selective solvent for biomass‑derived molecules, including lignin fragments and platform chemicals, due to its ability to disrupt hydrogen‑bond networks.

Catalysis and Reaction Media

  • Reaction medium for alkylation, acylation, and nucleophilic substitution, where the PF₆⁻ anion provides low coordinating strength and stabilizes reactive intermediates.
  • Support phase for immobilized catalysts, enabling biphasic catalysis and simplified product separation.

Energy, Tribology, and Environmental Applications

  • Component in ionic‑liquid‑based lubricants, where the C9 chain contributes to boundary‑layer formation, thermal stability, and reduced wear.
  • Absorption medium for selective gas capture (e.g., SO₂, light hydrocarbons), leveraging tunable hydrophobicity and ionic interactions.

Analytical and Spectroscopic Uses

  • Matrix and solvent for spectroscopic studies requiring low volatility and high thermal stability.
  • Medium for electroanalytical measurements, improving signal stability and reducing solvent evaporation.

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Additional information

Weight 25 g
Qty

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