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89483

Sigma-Aldrich

1-Ethyl-3-methylimidazolium bromide

≥97.0% (T)

Synonym(s):

1-Ethyl-3-methyl-1H-imidazolium bromide, 1-Methyl-3-ethylimidazolium bromide

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About This Item

Empirical Formula (Hill Notation):
C6H11BrN2
CAS Number:
Molecular Weight:
191.07
Beilstein:
5162084
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97.0% (T)

form

crystals

SMILES string

[Br-].CCn1cc[n+](C)c1

InChI

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

InChI key

GWQYPLXGJIXMMV-UHFFFAOYSA-M

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Application

1-Ethyl-3-methylimidazolium bromide can be used to prepare:
  • 1-ethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide
  • 1-ethyl-3-methylimidazolium tetrafluoroborate
  • (EMI)[Cd(BTC)] (EMI = 1-ethyl-3-methylimidazolium, BTC = 1,3,5-benzenetricarboxylate), a coordination polymer

Other Notes

Hydrophobic, highly conductive imidazolium molten salt melting at ambient temp.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Voltammetry of oxygen in the room-temperature ionic liquids 1-ethyl-3-methylimidazolium bis ((trifluoromethyl) sulfonyl) imide and hexyltriethylammonium bis ((trifluoromethyl) sulfonyl) imide: one-electron reduction to form superoxide. Steady-state and transient behavior......
Buzzeo MC, et al.
The Journal of Physical Chemistry A, 107(42), 8872-8878 (2003)
The phase behaviour of 1-alkyl-3-methylimidazolium tetrafluoroborates; ionic liquids and ionic liquid crystals.
J. Chem. Soc., Dalton Trans., 13, 2133-2140 (1999)
Ionic liquid as solvent for the synthesis and crystallization of a coordination polymer:(EMI)[Cd(BTC)](EMI=1-ethyl-3-methylimidazolium,BTC=1,3,5 benzenetricarboxylate).
Liao JH, et al.
Crystal Growth & Design, 6(5), 1062-1063 (2006)
Seungmin Oh et al.
The journal of physical chemistry. B, 123(39), 8274-8284 (2019-09-11)
Ionic liquids with aprotic heterocyclic anions (AHAs) have been developed for CO2 capture but have been considered for other applications as well. Previously, we have shown that AHA ILs, where the only site for reaction with CO2 is the anion
Pierre Bonhôte et al.
Inorganic chemistry, 35(5), 1168-1178 (1996-02-28)
New, hydrophobic ionic liquids with low melting points (<-30 degrees C to ambient temperature) have been synthesized and investigated, based on 1,3-dialkyl imidazolium cations and hydrophobic anions. Other imidazolium molten salts with hydrophilic anions and thus water-soluble are also described.

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