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Safety Information

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
Pricing and availability is not currently available.

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

53096-25G:
53096-BULK:
53096-VAR:
53096-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5166
BCCD8499
BCCB0902
BCBV6793
BCBR0831V

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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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