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Sigma-Aldrich

1-Butyl-2,3-dimethylimidazolium chloride

≥97.0% (HPLC/AT)

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About This Item

Formula empirica (notazione di Hill):
C9H17ClN2
Numero CAS:
98892-75-2
Peso molecolare:
188.70
Numero MDL:
MFCD03093291
Codice UNSPSC:
12352100
ID PubChem:
57652732
NACRES:
NA.22

Saggio

≥97.0% (HPLC/AT)

Forma fisica

crystals

Impurezze

≤1.0% water

Stringa SMILE

[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
HHHYPTORQNESCU-UHFFFAOYSA-M

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Categorie correlate

Applicazioni

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.

Stato fisico

ionic liquid

Altre note

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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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.
Royal Society of Chemistry Advances, 9(21), 11894-11900 (2019)
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
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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