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91508

Sigma-Aldrich

1-Butyl-3-methylimidazolium tetrafluoroborate

≥97.0% (HPLC)

Synonym(s):

BMIMBF4

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About This Item

Empirical Formula (Hill Notation):
C8H15BF4N2
CAS Number:
Molecular Weight:
226.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97.0% (HPLC)

form

liquid

density

1.21 g/mL at 20 °C (lit.)

SMILES string

F[B-](F)(F)F.CCCCn1cc[n+](C)c1

InChI

1S/C8H15N2.BF4/c1-3-4-5-10-7-6-9(2)8-10;2-1(3,4)5/h6-8H,3-5H2,1-2H3;/q+1;-1

InChI key

LSBXQLQATZTAPE-UHFFFAOYSA-N

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Application

1-Butyl-3-methylimidazolium tetrafluoroborate may be used as an extractant for the removal of dibenzothiophene (DBS) from liquid fuels via extractive desulfurization.

Other Notes

Ionic liquid used in many reactions, e.g. hydrogenations; asymmetric hydrogenations proceed in higher enantioselectivity than in homogeneous phase; Suzuki cross-coupling at ambient temperature

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

550.4 °F

Flash Point(C)

288 °C

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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C.J. Mathews et al.
Chemical Communications (Cambridge, England), 1249-1249 (2000)
Toshiyuki Wako et al.
Scientific reports, 10(1), 8948-8948 (2020-06-04)
During cell division, mitotic chromosomes assemble and are equally distributed into two new daughter cells. The chromosome organisation of the two chromatids is essential for even distribution of genetic materials. Although the 11-nm fibre or nucleosome structure is well-understood as
A.L. Monteiro et al.
Tetrahedron Asymmetry, 8, 177-177 (1997)
P.J. Dyson et al.
Chemical Communications (Cambridge, England), 25-25 (1999)
Preparation of 1?Butyl?3?Methyl Imidazolium?Based Room Temperature Ionic Liquids
Dupont, Jairton, et al.
Organic Syntheses, 236-236 (2003)

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