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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

PRTR

Class I Designated Chemical Substances

JAN Code

91508-BULK:
91508-VAR:
91508-INTR:
91508-250G:4548173183244
91508-50G:4548173183251
91508-5G:4548173183268


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)
Preparation of 1?Butyl?3?Methyl Imidazolium?Based Room Temperature Ionic Liquids
Dupont, Jairton, et al.
Organic Syntheses, 236-236 (2003)
P.J. Dyson et al.
Chemical Communications (Cambridge, England), 25-25 (1999)
Dahye Ji et al.
Scientific reports, 5, 16362-16362 (2015-11-10)
The AgO nanoparticles were utilized for a CO2 separation membrane. The AgO nanoparticles were successfully generated in ionic liquid 1-butyl-3-methyl imidazolium tetrafluoroborate (BMIMBF4) by favorable interaction between the surface of particles and the counteranion of BMIMBF4. The generated AgO nanoparticles
Synthesis, characterization and application of 1-butyl-3-methylimidazolium tetrafluoroborate for extractive desulfurization of liquid fuel.
Dharaskar SA, et al.
Arabian Journal of Chemistry, 9(4), 578-587 (2016)

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