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Sigma-Aldrich

1-Ethyl-3-methylimidazolium hexafluorophosphate

≥97.0% (HPLC)

Synonym(s):

EMIMPF6

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About This Item

Empirical Formula (Hill Notation):
C6H11F6N2P
CAS Number:
Molecular Weight:
256.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥97.0% (HPLC)

form

solid

mp

58-62 °C (lit.)
58-62 °C

SMILES string

F[P-](F)(F)(F)(F)F.CCn1cc[n+](C)c1

InChI

1S/C6H11N2.F6P/c1-3-8-5-4-7(2)6-8;1-7(2,3,4,5)6/h4-6H,3H2,1-2H3;/q+1;-1

InChI key

DPDAKOVGQUGTHH-UHFFFAOYSA-N

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General description

1-Ethyl-3-methylimidazolium hexafluorophosphate is a task-specific ionic liquid (TSIL) with low melting point.

Other Notes

Air- and water-stable immonium salt that is an ionic liquid at moderately elevated temperature, useful in molten salt technique

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J. Fuller et al.
Journal of the Chemical Society. Chemical Communications, 299-299 (1994)
Capillary electrophoretic application of 1-alkyl-3-methylimidazolium-based ionic liquids.
Yanes EG, et al.
Analytical Chemistry, 73(16), 3838-3844 (2001)
High-pressure phase behavior of systems with ionic liquids: II. The binary system carbon dioxide+ 1-ethyl-3-methylimidazolium hexafluorophosphate
Shariati, A., and C. J. Peters
Journal of Supercritical Fluids, 29.1, 43-48 (2004)
Rotational dynamics of a diatomic solute in the room-temperature ionic liquid 1-ethyl-3-methylimidazolium hexafluorophosphate
Shim, Youngseon, et al.
J. Chem. Phys. , 125.6 (2006)
Molecular dynamics studies of melting and some liquid-state properties of 1-ethyl-3-methylimidazolium hexafluorophosphate [emim][PF 6]
Alavi, Saman, and Donald L. Thompson
J. Chem. Phys. , 122.15, 154704-154704 (2005)

Articles

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

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