348414
1-Butylimidazole
98%
Synonym(s):
1-Butyl-1H-imidazole, 1-n-Butylimidazole, N-(n-Butyl)imidazole, N-Butyl-1H-imidazole, N-Butylimidazole, N-Butylimidazolium
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About This Item
Empirical Formula (Hill Notation):
C7H12N2
CAS Number:
Molecular Weight:
124.18
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-335-9
Beilstein/REAXYS Number:
109499
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.480 (lit.)
bp
114-116 °C/12 mmHg (lit.)
density
0.945 g/mL at 25 °C (lit.)
SMILES string
CCCCn1ccnc1
InChI
1S/C7H12N2/c1-2-3-5-9-6-4-8-7-9/h4,6-7H,2-3,5H2,1H3
InChI key
MCMFEZDRQOJKMN-UHFFFAOYSA-N
General description
1-Butylimidazole acts as an N-coordinated ligand. 1-Butylimidazole is formed as intermediate during the synthesis of a cationic cyclodextrin, used in the chiral separation of amino acids and anionic pharmaceuticals by capillary electrophoresis. Influence of 1-butylimidazole as base on the synthesis of dissymmetric chlorohydrin ester has been reported.
Application
1-Butylimidazole may be used in the synthesis of a heterocyclic mesomeric betaine. It was used in the synthesis of 1-(1-butyl-3-imidazolio)propane-3-sulfonate (BIm3S).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
293.0 °F
flash_point_c
145 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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A study of intravascular platelet aggregation by continuous platelet counting.
G M Smith et al.
Thrombosis research, 23(3), 275-288 (1981-08-01)
Viktoriya Polevaya et al.
Materials (Basel, Switzerland), 12(17) (2019-08-31)
The work is devoted to the chemical modification of a polymer that is promising for the creation of gas separation membranes, aimed at increasing the selectivity with respect to CO2. The introduction of ionic liquids into the structure of poly(1-trimethylsilyl-1-propyne)
Nina Gonsior et al.
Beilstein journal of organic chemistry, 8, 390-397 (2012-04-18)
The synthesis of a heterocyclic mesomeric betaine by quaternization reaction of 1-butylimidazole and tetrabromo-1,4-benzoquinone is presented. The structure was verified by means of X-ray single-crystal analysis, NMR and IR spectroscopy. Inclusion complexes of the heterocyclic mesomeric betaine with randomly methylated