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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

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)

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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.
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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
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
Quan Cao et al.
Carbohydrate research, 346(7), 956-959 (2011-04-05)
Conversion of fructose and glucose into 5-hydroxymethylfurfural (HMF) was investigated in various imidazolium ionic liquids, including 1-butyl-3-methylimidazolium chloride (BmimCl), 1-hexyl-3-methylimidazolium chloride (HmimCl), 1-octyl-3-methylimidazolium chloride (OmimCl), 1-benzyl-3-methylimidazolium chloride (BemimCl), 1-Butyl-2,3-dimethylimidazolium chloride (BdmimCl), and 1-butyl-3-methylimidazolium p-toluenesulfonate (BmimPS). The acidic C-2 hydrogen of

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Task-Specific Ionic Liquids

Task-Specific Ionic Liquids (TSILs) for the selective liquid/liquid extraction of heavy metals from aqueous systems were first published by Robin D. Rogers et al. in the year 2001.

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