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53096

Sigma-Aldrich

1-Ethyl-3-methylimidazolium chloride

dry, ≥98.0% (T)

Synonym(s):

1-Methyl-3-ethylimidazolinium chloride, 1-Methyl-3-ethylimidazolium chloride, 3-Ethyl-1-methylimidazolium chloride, N-Methyl-N′-ethylimidazolium chloride

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About This Item

Empirical Formula (Hill Notation):
C6H11ClN2
CAS Number:
65039-09-0
Molecular Weight:
146.62
Beilstein:
5163190
MDL number:
MFCD00074843
UNSPSC Code:
12352100
PubChem Substance ID:
57651397
NACRES:
NA.22

Assay

≥98.0% (T)

form

solid

impurities

≤800 ppm water

mp

77-79 °C (lit.)

SMILES string

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

InChI

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

InChI key

BMQZYMYBQZGEEY-UHFFFAOYSA-M

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

370.4 °F - closed cup

Flash Point(C)

188 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Anshu Sharma et al.
Carbohydrate polymers, 134, 617-626 (2015-10-03)
Ionic liquids (IL) can alter the physical properties of agar hydrogels. Rheology studies show that gels with wide range of storage moduli (gel strength) G0 values ranging from 1 to 20 KPa could be made in imidazolium based IL solutions
M T Ubeda-Torres et al.
Journal of chromatography. A, 1380, 96-103 (2015-01-17)
In reversed-phase liquid chromatography in the absence of additives, cationic basic compounds give rise to broad and asymmetrical peaks as a result of ionic interactions with residual free silanols on silica-based stationary phases. Ionic liquids (ILs), added to the mobile

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