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Sigma-Aldrich

1-Butyl-2,3-dimethylimidazolium chloride

≥97.0% (HPLC/AT)

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About This Item

Formule empirique (notation de Hill):
C9H17ClN2
Numéro CAS:
98892-75-2
Poids moléculaire :
188.70
Numéro MDL:
MFCD03093291
Code UNSPSC :
12352100
ID de substance PubChem :
57652732
Nomenclature NACRES :
NA.22

Pureté

≥97.0% (HPLC/AT)

Forme

crystals

Impuretés

≤1.0% water

Chaîne SMILES 

[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

Clé InChI

HHHYPTORQNESCU-UHFFFAOYSA-M

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Catégories apparentées

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.

Forme physique

ionic liquid

Autres remarques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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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
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
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)
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)
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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