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Sigma-Aldrich

1-Butyl-2,3-dimethylimidazolium chloride

≥97.0% (HPLC/AT)

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About This Item

Empirical Formula (Hill Notation):
C9H17ClN2
CAS Number:
98892-75-2
Molecular Weight:
188.70
MDL number:
MFCD03093291
UNSPSC Code:
12352100
PubChem Substance ID:
57652732
NACRES:
NA.22

Quality Level

100

Assay

≥97.0% (HPLC/AT)

form

crystals

impurities

≤1.0% water

SMILES string

[Cl-].CCCCn1cc[n+](C)c1C

InChI

1S/C9H17N2.ClH/c1-4-5-6-11-8-7-10(3)9(11)2;/h7-8H,4-6H2,1-3H3;1H/q+1;/p-1

InChI key

HHHYPTORQNESCU-UHFFFAOYSA-M

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Application

1-Butyl-2,3-dimethylimidazolium chloride can be used:
  • As a solvent in the chemical modification of polysaccharide cellulose.
  • As a model ionic liquid in the conversion of a monosaccharide like fructose into 5-hydroxymethylfurfural using H2SO4.
  • To prepare 1-butyl-2,3-dimethylimidazolium dicarba-7,8-nidoundecaborate by reacting with caesium dicarba-7,8-nido-undecaborate.
  • To prepare mesoporous ZnAl2O4 nanomaterials, which are used as catalysts or catalyst supports.

Physical form

ionic liquid

Other Notes

Ionic liquid suitable for use in strongly basic conditions, e.g. for oxidations and metathesis reactions

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

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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Yanqi Wang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(7), 1624-1632 (2020-01-24)
Although supertetrahedral Tn sulfide clusters (n=2-6) have been extensively explored, the synthesis of Tn selenide clusters with n>4 has not been achieved thus far. Reported here are ionic-liquid (IL)-assisted precursor route syntheses, characterizations, and the photocatalytic properties of six new
Crystal structure of 1-butyl-2, 3-dimethylimidazolium dicarba-7, 8-nido-undecaborate
Klemes MJ, et al.
Acta Crystallographica Section E: Crystallographic Communications, 71(3), o183-o183 (2015)
Preparation of mesoporous ZnAl2O4 nanoflakes by ion exchange from a Na-dawsonite parent material in the presence of an ionic liquid
Kim T, et al.
Royal Society of Chemistry Advances, 9(21), 11894-11900 (2019)
Bertram Peters et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(70), 16683-16689 (2020-09-03)
Multinary chalcogenido (semi)metalate salts exhibit finely tunable optical properties based on the combination of metal and chalcogenide ions in their polyanionic substructure. Here, we present the structural expansion of chalcogenido germanate(IV) or stannate(IV) architectures with SbIII , which clearly affects
Interactions of ionic liquids with polysaccharides-2: Cellulose
Heinze T, et al.
Macromolecular Symposia, 262(1), 8-22 (2008)
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Articles

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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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