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1-n-Butyl-3-methylimidazolium hexafluorophosphate_Molecular_structure_CAS_174501-64-5)
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1-n-Butyl-3-methylimidazolium hexafluorophosphate

Catalog No. L19086 Name Alfa Aesar
CAS Number 174501-64-5 Website
M. F. C8H15F6N2P Telephone
M. W. 284.1822802 Fax
Purity 98+% Email
Storage Chembase ID: 11867

SYNONYMS

Title
1-正-丁基-3-甲基咪唑鎓六氟磷酸盐
IUPAC name
1-butyl-3-methyl-1H-imidazol-3-ium; hexafluoro-λ5-phosphanuide
IUPAC Traditional name
1-butyl-3-methylimidazolium hexafluorophosphate
Synonyms
BMIMPF6

DATABASE IDS

CAS Number 174501-64-5
EC Number 000-000-0
Merck Index 141581
MDL Number MFCD03093295

PROPERTIES

Purity 98+%
Boiling Point >350°C
Density 1.365
Melting Point 8-10°C
Refractive Index 1.4115
GHS Pictograms GHS07
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
GHS Precautionary statements P261-P305+P351+P338-P302+P352-P321-P405-P501A
Risk Statements 36/37/38
Safety Statements 26-37
TSCA Listed

DETAILS

REFERENCES

  • A copper-free Sonogashira coupling of terminal alkynes with aryl iodides, catalyzed by trans-Dichlorobis(triphenylphosphine)palladium(II), 10491, has been adapted to a microflow system for efficient catalyst recycling: Org. Lett., 4, 1691 (2002).
  • Ionic liquid.
  • For use in dihydroxylation of alkenes with Osmium(VIII) oxide, 12103, facilitating the reuse of the Os catalyst, see: Org. Lett., 4, 2197 (2002).
  • Recyclable medium for oxidation of alcohols, catalyzed by TEMPO, A12733, and CuCl, to give aldehydes and ketones chemoselectively under mild conditions: Org. Lett., 4, 1507 (2002).
  • Heck reactions with aryl halides can be carried out with controlled microwave heating: J. Org. Chem., 67, 6243 (2002).