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Sigma-Aldrich

1-Butyl-3-methylimidazolium tetrachloroaluminate

95%

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About This Item

Empirical Formula (Hill Notation):
C8H15AlCl4N2
CAS Number:
80432-09-3
Molecular Weight:
308.01
MDL number:
MFCD06798193
UNSPSC Code:
12352100
PubChem Substance ID:
57651523
NACRES:
NA.22

Assay

≥94.5% (HPLC)
95%

SMILES string

Cl[Al-](Cl)(Cl)Cl.CCCCn1cc[n+](C)c1

InChI

1S/C8H15N2.Al.4ClH/c1-3-4-5-10-7-6-9(2)8-10;;;;;/h6-8H,3-5H2,1-2H3;;4*1H/q+1;+3;;;;/p-4

InChI key

PNOZWIUFLYBVHH-UHFFFAOYSA-J

Related Categories

General description

1-Butyl-3-methylimidazolium tetrachloroaluminate is an ionic liquid that can be prepared by reacting 1-butyl-3-methylimidazolium chloride with aluminum chloride hexahydrate.

Application

1-Butyl-3-methylimidazolium tetrachloroaluminate can be used as an efficient catalyst in tetrahydropyranylation of alcohols, and detetrahydropyranylation of THP (tetrahydropyranyl) protected ethers.
It can also be used as:
  • A catalyst to synthesize linear alkylbenzenes by alkylation of benzene with 1-dodecene.
  • A solvent in extractive desulfurization of oil products.

Signal Word

Danger

Hazard Statements

H302,H314,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

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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Microwave-assisted preparation of dialkylimidazolium tetrachloroaluminates and their use as catalysts in the solvent-free tetrahydropyranylation of alcohols and phenols
Namboodiri VV and Varma RS
Chemical Communications (Cambridge, England), 342-343 (2002)
Microwave-assisted preparation of dialkylimidazolium tetrachloroaluminates and their use as catalysts in the solvent-free tetrahydropyranylation of alcohols and phenols.
Namboodiri VV and Varma RS.
Chemical Communications (Cambridge, England), 4, 342-343 (2002)
Oil products desulfurization by 1-butyl-3-methylimidazolium tetrachloroaluminate ionic liquid: Experimental study and thermodynamic modelling
Fazlali A, et al.
Journal of Molecular Liquids, 237(1-2), 437-446 (2017)
Sylwia Bajkacz et al.
Molecules (Basel, Switzerland), 25(20) (2020-10-21)
A novel, efficient extraction procedure based on natural deep eutectic solvents (NADES) and ionic liquids (ILs) for determination of 20-hydroxyecdysone (20-E) in spinach has been developed. NADES, the first green extraction agent, with different hydrogen bond donors and acceptors are
Activity and stability investigation of [BMIM][AlCl4] ionic liquid as catalyst for alkylation of benzene with 1-dodecene
Qiao C-Z, et al.
Applied Catalysis A: General, 276(1-2), 61-66 (2004)
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BASIONICS™ Ionic Liquids

BASIONICS™ Ionic Liquids offer diverse properties for varied applications in the BASF portfolio.

BASIONICS™ Ionic Liquids

BASIONICS™ Ionic Liquids offer diverse properties for varied applications in the BASF portfolio.

BASIONICS™ Ionic Liquids

BASIONICS™ Ionic Liquids offer diverse properties for varied applications in the BASF portfolio.

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