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87929

Sigma-Aldrich

1-Hexyl-3-methylimidazolium chloride

≥97.0% (HPLC)

Synonym(s):

HMIMCl

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About This Item

Empirical Formula (Hill Notation):
C10H19ClN2
CAS Number:
Molecular Weight:
202.72
Beilstein:
8356525
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97.0% (HPLC)

form

liquid

SMILES string

[Cl-].CCCCCCn1cc[n+](C)c1

InChI

1S/C10H19N2.ClH/c1-3-4-5-6-7-12-9-8-11(2)10-12;/h8-10H,3-7H2,1-2H3;1H/q+1;/p-1

InChI key

NKRASMXHSQKLHA-UHFFFAOYSA-M

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General description

1-hexyl-3-methylimidazolium chloride is an ionic liquid (IL). Its surface and bulk properties in aqueous solution at various temperatures indicates that it behaves as a short-chain cationic surfactant and shows aggregation behavior.

Physical form

Ionic solvent, liquid salt

Other Notes

Ionic liquid employed in the catalytic, solvent-free alkylation; catalyst for polymerization of olefins.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Dynamic viscosities of a series of 1-alkyl-3-methylimidazolium chloride ionic liquids and their binary mixtures with water at several temperatures
Gomez, Elena, et al.
Journal of Chemical and Engineering Data, 51.2, 696-701 (2006)
Solution enthalpies of ionic liquid 1-hexyl-3-methylimidazolium chloride
Fang, Da-Wei, Ying-Chun Sun, and Zhen-Wei Wang
Journal of Chemical and Engineering Data, 53.1, 259-261 (2007)
Physical properties of the ternary mixture ethanol+ water+ 1-hexyl-3-methylimidazolium chloride at 298.15 K
Gomez, E., et al.
Physics and Chemistry of Liquids, 44.4, 409-417 (2006)
Homogeneous Tritylation of Cellulose in 1?Butyl?3?methylimidazolium Chloride
Erdmenger, Tina, et al.
Macromolecular Bioscience, 7.4, 440-445 (2007)
Vasudevan V Namboodiri et al.
Chemical communications (Cambridge, England), (4), 342-343 (2002-07-18)
Microwave-assisted preparation of dialkylimidazolium tetrachloroaluminates, [CnMIM][AlCl4] and their application as recyclable catalysts for the efficient and eco-friendly protection of alcohols as tetrahydropyranyl (THP) ethers are described. The same catalyst can also be utilized for the deprotection of THP ethers.

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