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Safety Information

73244

Sigma-Aldrich

1-Hexyl-3-methylimidazolium tetrafluoroborate

≥97.0% (HPLC)

Synonym(s):

HMIMBF4

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About This Item

Empirical Formula (Hill Notation):
C10H19BF4N2
CAS Number:
244193-50-8
Molecular Weight:
254.08
Beilstein:
8366236
MDL number:
MFCD03095459
UNSPSC Code:
12352100
PubChem Substance ID:
57652467
NACRES:
NA.22

Quality Level

100

Assay

≥97.0% (HPLC)

form

liquid

impurities

≤1.0% water

refractive index

n20/D 1.430

density

1.149 g/mL at 20 °C (lit.)

SMILES string

F[B-](F)(F)F.CCCCCCn1cc[n+](C)c1

InChI

1S/C10H19N2.BF4/c1-3-4-5-6-7-12-9-8-11(2)10-12;2-1(3,4)5/h8-10H,3-7H2,1-2H3;/q+1;-1

InChI key

MFXLOVLEQJRXFP-UHFFFAOYSA-N

Other Notes

Enzyme catalysis in ionic liquids

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

No data available

Flash Point(C)

No data available

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

73244-VAR:
73244-BULK:
73244-50G:4548173179131
73244-5G:4548173179148

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF6118
BCBG1979V
1402471V
1402471
1314525

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S.H. Schofer et al.
Chemical Communications (Cambridge, England), 425-425 (2001)
E Diaz et al.
Ecotoxicology and environmental safety, 162, 29-34 (2018-07-01)
The ecotoxicity and inhibition of 12 imidazolium ionic liquids (ILs) with alkyl chain from C4 to C10 and chloride (Cl-), tetrafluoroborate (BF4-) and bis(trifluoromethanesulfonyl)imide (NTf2-) anions have been studied by means of respiration inhibition assays using activated sludge collected from
Renata Kołodziejska et al.
Chirality, 30(2), 206-214 (2017-11-16)
The application of ionic liquids as solvents for transesterification of prochiral pirymidine acyclonucleoside using lipase (EC 3.1.1.3) Amano PS from Burkholderia cepacia (BCL) is reported. The effect of using medium reaction, acyl group donor, and temperature on the activity and
Kunze Du et al.
Food chemistry, 244, 190-196 (2017-11-10)
A simple and green ionic liquid-based vortex-forced matrix solid phase dispersion (IL-VFMSPD) method was presented to simultaneously extract 5-hydroxymethyl furfurol (5-HMF) and iridoid glycosides in Fructus Corni by ultra-high performance liquid chromatography. Ionic liquid was used as a green elution
Sylwia Bajkacz et al.
Molecules (Basel, Switzerland), 25(14) (2020-07-18)
This work aimed to comprehensively evaluate the potential and effectiveness of deep eutectic solvents (DESs) in the extraction of seven catechins from various tea samples. Different combinations of DES were used, consisting of Girard's reagent T (GrT) in various mixing

Protocols

Enzymatic Reactions in Ionic Liquids

One of the most popular lipase for synthetic use is the Candida antarctica lipase (CALB). CALB catalyzes the enantioselective acylation of 1-phenylethylamine with 4-pentenoic acid

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